Tina Coenen, Matthias Maerevoet, Stephanie Chen, Mathias De Brouwer, Sofie Van Hoecke, Ernst Hw Koster, Mariek Mp Vanden Abeele, Klaas Bombeke
Background: Major depressive disorder is often a recurrent condition, with a high risk of relapse for individuals remitted from depression. Early detection of relapse is critical to improve clinical outcomes. Mobile health (mHealth) technologies offer new opportunities for real-time monitoring and prevention of relapse, if the user requirements of the target population are effectively implemented.
Objective: This study investigated the requirements and concerns of individuals remitted from depression for an mHealth app aimed at monitoring depressive symptoms and detecting early signs of relapse through integrating both active ecological momentary assessment data and passive data from the user's smartphone and smartwatch.
Methods: Three focus group discussions were conducted with 17 participants remitted from depression. Before the focus group, participants had gained some experience with an in-house designed ecological momentary assessment monitoring app, prompting questions regarding their mood multiple times throughout the day. During the focus groups, feedback and insights were gathered on participants' expectations, requirements, concerns, and attitudes toward a depression monitoring app. A thematic analysis was performed to identify recurring themes and subthemes, shedding light on the desired user experience and functionalities.
Results: We identified 5 main themes. Participants highlighted (1) a need for customization settings, particularly in terms of data collection and sharing, and frequency of self-assessments. They also valued (2) positivity in the app's design through positive reinforcement and journaling features. Additionally, participants emphasized (3) interventions to be the main motivator for adoption and long-term usage. More specifically, they wanted the app to foster self-awareness, self-reflection, and insights, and to offer support during deteriorations in mental health. Furthermore, participants deemed (4) transparency in data use and machine learning predictions to be essential for building trust. Participants required these functionalities to bear (5) the user burdens of self-monitoring. Key concerns were for passive monitoring to cause a privacy burden and for active monitoring to raise an emotional burden.
Conclusions: Considering the vulnerability of potential users, the design of an mHealth app for early depression relapse detection should be guided by user preferences and approached with caution. Requirements for customization, positivity, interventions, and transparency must be addressed, while minimizing both the emotional and privacy burden. Future iterations should implement these findings to improve and test the app's acceptability, adoption, and usability for clinical use.
{"title":"Requirements and Concerns of Individuals Remitted From Depression for an Early Relapse Detection mHealth App: Focus Group Study.","authors":"Tina Coenen, Matthias Maerevoet, Stephanie Chen, Mathias De Brouwer, Sofie Van Hoecke, Ernst Hw Koster, Mariek Mp Vanden Abeele, Klaas Bombeke","doi":"10.2196/67141","DOIUrl":"10.2196/67141","url":null,"abstract":"<p><strong>Background: </strong>Major depressive disorder is often a recurrent condition, with a high risk of relapse for individuals remitted from depression. Early detection of relapse is critical to improve clinical outcomes. Mobile health (mHealth) technologies offer new opportunities for real-time monitoring and prevention of relapse, if the user requirements of the target population are effectively implemented.</p><p><strong>Objective: </strong>This study investigated the requirements and concerns of individuals remitted from depression for an mHealth app aimed at monitoring depressive symptoms and detecting early signs of relapse through integrating both active ecological momentary assessment data and passive data from the user's smartphone and smartwatch.</p><p><strong>Methods: </strong>Three focus group discussions were conducted with 17 participants remitted from depression. Before the focus group, participants had gained some experience with an in-house designed ecological momentary assessment monitoring app, prompting questions regarding their mood multiple times throughout the day. During the focus groups, feedback and insights were gathered on participants' expectations, requirements, concerns, and attitudes toward a depression monitoring app. A thematic analysis was performed to identify recurring themes and subthemes, shedding light on the desired user experience and functionalities.</p><p><strong>Results: </strong>We identified 5 main themes. Participants highlighted (1) a need for customization settings, particularly in terms of data collection and sharing, and frequency of self-assessments. They also valued (2) positivity in the app's design through positive reinforcement and journaling features. Additionally, participants emphasized (3) interventions to be the main motivator for adoption and long-term usage. More specifically, they wanted the app to foster self-awareness, self-reflection, and insights, and to offer support during deteriorations in mental health. Furthermore, participants deemed (4) transparency in data use and machine learning predictions to be essential for building trust. Participants required these functionalities to bear (5) the user burdens of self-monitoring. Key concerns were for passive monitoring to cause a privacy burden and for active monitoring to raise an emotional burden.</p><p><strong>Conclusions: </strong>Considering the vulnerability of potential users, the design of an mHealth app for early depression relapse detection should be guided by user preferences and approached with caution. Requirements for customization, positivity, interventions, and transparency must be addressed, while minimizing both the emotional and privacy burden. Future iterations should implement these findings to improve and test the app's acceptability, adoption, and usability for clinical use.</p>","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":"13 ","pages":"e67141"},"PeriodicalIF":6.2,"publicationDate":"2025-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12592899/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145354551","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Walter Staiano, Christine E Callahan, Michelle Davis, Leah Tanner, Sarah Kunkle, Jenna Glover, Jon Kole, Neeru Bakshi, Marco Romagnoli, Ulrich Kirk
<p><strong>Background: </strong>Anxiety and depressive disorders affect hundreds of millions globally, with substantial barriers limiting access to evidence-based treatments like cognitive behavioral therapy. Digital mental health interventions offer potential solutions to improve access to support. However, evidence of efficacy through randomized controlled trials is essential for clinical adoption.</p><p><strong>Objective: </strong>This study evaluated the efficacy of the Headspace Anxiety and Depression Program, a digitally delivered 21-session intervention grounded in the Unified Protocol that integrates cognitive behavioral and mindfulness-based strategies to target common drivers of emotional disorders, compared to a waitlist control group. Primary aims were to assess reductions in anxiety (Generalized Anxiety Disorder-7 [GAD-7]) and depression (Patient Health Questionnaire-8 [PHQ-8]) symptoms. Secondary aims examined improvements in sleep quality (Pittsburgh Sleep Quality Index), perceived stress (Perceived Stress Scale-10), mindfulness (Mindful Attention Awareness Scale), and overall well-being (Warwick-Edinburgh Mental Well-Being Scale), as well as clinical remission and treatment response rates.</p><p><strong>Methods: </strong>A fully remote, 2-arm parallel-group randomized controlled trial was conducted with 168 participants (aged ≥18 years) who had clinically significant anxiety (GAD-7≥10) or depression symptoms (PHQ-8≥10). Participants were randomized to either the Headspace Anxiety and Depression Program (n=84) or waitlist control (n=84). The intervention consisted of 21 daily sessions (5-10 minutes each) delivered via the Headspace app. Primary (GAD-7 and PHQ-8) and secondary outcomes (Pittsburgh Sleep Quality Index, Perceived Stress Scale-10, Mindful Attention Awareness Scale, and Warwick-Edinburgh Mental Well-Being Scale) were assessed at baseline, postintervention, and a 3-week follow-up using intention-to-treat analysis with mixed-model ANOVAs.</p><p><strong>Results: </strong>Study retention was high, with the majority (154/168, 91.7%) of participants completing the 3-week follow-up visit, and no serious adverse events were reported. Intervention adherence was high, with 82.1% (69/84) in the intervention group completing all 21 sessions. Significant group×time interactions were observed for both primary outcomes (P<.001). The Headspace group showed substantial reductions in anxiety symptoms (GAD-7: 34.5% reduction from baseline: mean 11.9, SD 2.8 to follow-up: mean 7.8, SD 2.3; η<sup>2</sup><sub>p</sub>=0.350) and depression symptoms (PHQ-8: 33.9% reduction from baseline: mean 12.1, SD 2.8 to follow-up: mean 8.0, SD 2.0; η<sup>2</sup><sub>p</sub>=0.370), while the control group did not show significant reductions. Combined anxiety and depression remission rates were significantly higher in the Headspace group (18/84, 21.4%) versus controls (7/84, 8.3%; P=.03), as were treatment response rates (23/84, 27.3% vs 2/84, 2.3%; P=.03)
{"title":"Efficacy of a Self-Guided Transdiagnostic Intervention for Adults With Anxiety and Depression: Randomized Controlled Trial.","authors":"Walter Staiano, Christine E Callahan, Michelle Davis, Leah Tanner, Sarah Kunkle, Jenna Glover, Jon Kole, Neeru Bakshi, Marco Romagnoli, Ulrich Kirk","doi":"10.2196/79759","DOIUrl":"10.2196/79759","url":null,"abstract":"<p><strong>Background: </strong>Anxiety and depressive disorders affect hundreds of millions globally, with substantial barriers limiting access to evidence-based treatments like cognitive behavioral therapy. Digital mental health interventions offer potential solutions to improve access to support. However, evidence of efficacy through randomized controlled trials is essential for clinical adoption.</p><p><strong>Objective: </strong>This study evaluated the efficacy of the Headspace Anxiety and Depression Program, a digitally delivered 21-session intervention grounded in the Unified Protocol that integrates cognitive behavioral and mindfulness-based strategies to target common drivers of emotional disorders, compared to a waitlist control group. Primary aims were to assess reductions in anxiety (Generalized Anxiety Disorder-7 [GAD-7]) and depression (Patient Health Questionnaire-8 [PHQ-8]) symptoms. Secondary aims examined improvements in sleep quality (Pittsburgh Sleep Quality Index), perceived stress (Perceived Stress Scale-10), mindfulness (Mindful Attention Awareness Scale), and overall well-being (Warwick-Edinburgh Mental Well-Being Scale), as well as clinical remission and treatment response rates.</p><p><strong>Methods: </strong>A fully remote, 2-arm parallel-group randomized controlled trial was conducted with 168 participants (aged ≥18 years) who had clinically significant anxiety (GAD-7≥10) or depression symptoms (PHQ-8≥10). Participants were randomized to either the Headspace Anxiety and Depression Program (n=84) or waitlist control (n=84). The intervention consisted of 21 daily sessions (5-10 minutes each) delivered via the Headspace app. Primary (GAD-7 and PHQ-8) and secondary outcomes (Pittsburgh Sleep Quality Index, Perceived Stress Scale-10, Mindful Attention Awareness Scale, and Warwick-Edinburgh Mental Well-Being Scale) were assessed at baseline, postintervention, and a 3-week follow-up using intention-to-treat analysis with mixed-model ANOVAs.</p><p><strong>Results: </strong>Study retention was high, with the majority (154/168, 91.7%) of participants completing the 3-week follow-up visit, and no serious adverse events were reported. Intervention adherence was high, with 82.1% (69/84) in the intervention group completing all 21 sessions. Significant group×time interactions were observed for both primary outcomes (P<.001). The Headspace group showed substantial reductions in anxiety symptoms (GAD-7: 34.5% reduction from baseline: mean 11.9, SD 2.8 to follow-up: mean 7.8, SD 2.3; η<sup>2</sup><sub>p</sub>=0.350) and depression symptoms (PHQ-8: 33.9% reduction from baseline: mean 12.1, SD 2.8 to follow-up: mean 8.0, SD 2.0; η<sup>2</sup><sub>p</sub>=0.370), while the control group did not show significant reductions. Combined anxiety and depression remission rates were significantly higher in the Headspace group (18/84, 21.4%) versus controls (7/84, 8.3%; P=.03), as were treatment response rates (23/84, 27.3% vs 2/84, 2.3%; P=.03)","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":"13 ","pages":"e79759"},"PeriodicalIF":6.2,"publicationDate":"2025-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12592896/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145354580","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Tyler Prochnow, Wei-Lin Wang, Shirlene Wang, Jixin Li, Alexander J Rothman, Stephen S Intille, Donald Hedeker, Genevieve F Dunton
<p><strong>Background: </strong>Ecological momentary assessment (EMA) is a valuable method for capturing real-time data on behaviors and experiences in naturalistic settings. However, maintaining participant engagement in longitudinal (ie, multiburst) EMA studies remains challenging, particularly when collecting intensive data over extended periods. Understanding factors affecting completion rates is essential for designing more effective EMA protocols and interpreting results accurately.</p><p><strong>Objective: </strong>This study investigated factors influencing EMA completion rates in a 12-month intensive longitudinal study among young adults in the United States, examining both time-varying factors and stable individual characteristics.</p><p><strong>Methods: </strong>Young adults (N=246, ages 18-29 years) participated in the Temporal Influences on Movement and Exercise (TIME) study, responding to smartphone-based EMA prompts during biweekly measurement bursts (4-day periods of intensive sampling), with continuous passive data collection via smartwatches. Each burst included signal-contingent prompts delivered approximately once per hour during waking hours, resulting in an average of 12.1 (SD 1.3) prompts per day. Multilevel logistic regression models examined the effects of time-varying temporal factors (time of day, day of week, season, and time in study), contextual factors (phone screen status, phone usage, and location), behavioral factors (sleep duration, physical activity levels, and travel status), and psychological factors (momentary affect and stress) on prompt completion. Models also included time-invariant demographic characteristics (sex, race, ethnicity, education, and employment) and tested interactions between time in study and other predictors.</p><p><strong>Results: </strong>Mean completion rate was 77% (SD 13%). Hispanic participants showed lower odds of completion compared to non-Hispanic participants (odds ratio [OR] 0.79, 95% CI 0.63-0.99; P=.04) and employed participants were less likely to complete prompts than unemployed participants (OR 0.75, 95% CI 0.61-0.92; P<.01). Having the phone screen on at prompt delivery substantially increased completion odds (OR 3.39, 95% CI 2.81-4.09; P<.001), while being away from home reduced completion likelihood, with particularly low odds when at sports facilities (OR 0.58, 95% CI 0.47-0.74; P<.001) or restaurants and shops (OR 0.61, 95% CI 0.51-0.72; P<.001). Short sleep duration the previous night (OR 0.92, 95% CI 0.87-0.99; P=.02) and traveling status (OR 0.78, 95% CI 0.75-0.82; P<.001) were associated with lower completion odds. Higher momentary stress levels predicted lower completion of subsequent prompts (OR 0.85, 95% CI 0.78-0.93; P<.001). Completion odds declined over the 12-month study (OR 0.95, 95% CI 0.94-0.96; P<.001), with significant interactions between time in study and various predictors, indicating changing patterns of engagement over time.</p><p><strong>Conclusi
背景:生态瞬间评估(EMA)是一种捕捉自然环境中行为和体验的实时数据的有价值的方法。然而,在纵向(即多脉冲)EMA研究中保持参与者的参与度仍然具有挑战性,特别是在长时间收集密集数据时。了解影响完成率的因素对于设计更有效的EMA方案和准确解释结果至关重要。目的:本研究在美国年轻人中进行了为期12个月的密集纵向研究,研究了影响EMA完成率的因素,考察了时变因素和稳定的个体特征。方法:年轻人(N=246,年龄18-29岁)参加了运动和锻炼的时间影响(TIME)研究,在两周的测量爆发(4天的密集采样周期)中响应基于智能手机的EMA提示,通过智能手表连续被动收集数据。每次脉冲包括在清醒时大约每小时传递一次的信号相关提示,平均每天产生12.1次(SD 1.3)提示。多层逻辑回归模型检验了时变的时间因素(一天中的时间、一周中的哪一天、季节和学习时间)、背景因素(手机屏幕状态、手机使用情况和位置)、行为因素(睡眠时间、身体活动水平和旅行状况)和心理因素(瞬间影响和压力)对快速完成的影响。模型还包括时不变的人口特征(性别、种族、民族、教育和就业),并测试了学习时间和其他预测因素之间的相互作用。结果:平均完成率为77% (SD为13%)。与非西班牙裔受试者相比,西班牙裔受试者完成提示的几率较低(比值比[OR] 0.79, 95% CI 0.63-0.99; P= 0.04),就业受试者完成提示的可能性低于失业受试者(比值比[OR] 0.75, 95% CI 0.61-0.92;结论:研究结果强调了纵向多脉冲研究中EMA参与的动态性质,并强调了在研究设计和分析中考虑时变和时不变因素的重要性。这项研究为研究人员在行为科学和数字健康方面设计深入的纵向研究提供了有价值的见解。优化EMA协议的潜在策略可能包括根据个人情况定制提示时间表和开发自适应采样技术。
{"title":"Understanding Longitudinal Ecological Momentary Assessment Completion: Results From 12 Months of Burst Sampling in the TIME Study.","authors":"Tyler Prochnow, Wei-Lin Wang, Shirlene Wang, Jixin Li, Alexander J Rothman, Stephen S Intille, Donald Hedeker, Genevieve F Dunton","doi":"10.2196/67117","DOIUrl":"10.2196/67117","url":null,"abstract":"<p><strong>Background: </strong>Ecological momentary assessment (EMA) is a valuable method for capturing real-time data on behaviors and experiences in naturalistic settings. However, maintaining participant engagement in longitudinal (ie, multiburst) EMA studies remains challenging, particularly when collecting intensive data over extended periods. Understanding factors affecting completion rates is essential for designing more effective EMA protocols and interpreting results accurately.</p><p><strong>Objective: </strong>This study investigated factors influencing EMA completion rates in a 12-month intensive longitudinal study among young adults in the United States, examining both time-varying factors and stable individual characteristics.</p><p><strong>Methods: </strong>Young adults (N=246, ages 18-29 years) participated in the Temporal Influences on Movement and Exercise (TIME) study, responding to smartphone-based EMA prompts during biweekly measurement bursts (4-day periods of intensive sampling), with continuous passive data collection via smartwatches. Each burst included signal-contingent prompts delivered approximately once per hour during waking hours, resulting in an average of 12.1 (SD 1.3) prompts per day. Multilevel logistic regression models examined the effects of time-varying temporal factors (time of day, day of week, season, and time in study), contextual factors (phone screen status, phone usage, and location), behavioral factors (sleep duration, physical activity levels, and travel status), and psychological factors (momentary affect and stress) on prompt completion. Models also included time-invariant demographic characteristics (sex, race, ethnicity, education, and employment) and tested interactions between time in study and other predictors.</p><p><strong>Results: </strong>Mean completion rate was 77% (SD 13%). Hispanic participants showed lower odds of completion compared to non-Hispanic participants (odds ratio [OR] 0.79, 95% CI 0.63-0.99; P=.04) and employed participants were less likely to complete prompts than unemployed participants (OR 0.75, 95% CI 0.61-0.92; P<.01). Having the phone screen on at prompt delivery substantially increased completion odds (OR 3.39, 95% CI 2.81-4.09; P<.001), while being away from home reduced completion likelihood, with particularly low odds when at sports facilities (OR 0.58, 95% CI 0.47-0.74; P<.001) or restaurants and shops (OR 0.61, 95% CI 0.51-0.72; P<.001). Short sleep duration the previous night (OR 0.92, 95% CI 0.87-0.99; P=.02) and traveling status (OR 0.78, 95% CI 0.75-0.82; P<.001) were associated with lower completion odds. Higher momentary stress levels predicted lower completion of subsequent prompts (OR 0.85, 95% CI 0.78-0.93; P<.001). Completion odds declined over the 12-month study (OR 0.95, 95% CI 0.94-0.96; P<.001), with significant interactions between time in study and various predictors, indicating changing patterns of engagement over time.</p><p><strong>Conclusi","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":"13 ","pages":"e67117"},"PeriodicalIF":6.2,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12590043/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145344990","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ronald T Ackermann, Kenzie A Cameron, David T Liss, Nancy Dolan, Cassandra Aikman, Amy R Carson, Sterling A Harris, Kathryn Doyle, Andrew J Cooper, Brian Hitsman
Background: Intensive lifestyle interventions (ILI) improve weight loss and cardiovascular risk factors, but health care systems face challenges in implementing them. We engaged stakeholders to cocreate and evaluate primary care implementation strategies for ILI components.
Objective: This study aimed to describe the design of intervention components and implementation strategies and to evaluate the feasibility of pragmatic trial enrollment and randomization procedures, as well as the acceptability and preliminary effectiveness of the interventions.
Methods: The study setting was a single, urban primary care office. Patients with a BMI ≥27 kg/m² and ≥1 cardiovascular risk factor were sent a single electronic health record (EHR) message between December 2019 and January 2020 offering services to support a weight loss goal of 10 pounds in 10 weeks. All patients who affirmed interest were pragmatically enrolled in a trial offering basic lifestyle support (BLS), which provided a scale that transmits weight data to the EHR using cellular networks, a coupon to enroll in lifestyle coaching resources through a partnering fitness organization, and periodic EHR messages encouraging use of those resources. About half (n=42) of participants were randomized by an EHR algorithm to also receive customized lifestyle support (CLS), including weekly email messages adaptive to weight loss progress and telephonic coaching by a nurse for those facing challenges. Interventions and assessments spanned from January to July 2020, with disruption by the COVID-19 pandemic. Weight data were collected from administrative sources. Qualitative analysis of stakeholder recommendations and patient interviews assessed intervention acceptability, appropriateness, and sustainability.
Results: Over 6 weeks, 426 patients were sent the EHR invitation message, and 80 (18.8%) patients affirmed interest in the weight loss goal and were enrolled. Overall, 48 of 80 (60%) trial participants lost weight at 6 months; 12 (15%) exhibited weight loss ≥5%, with no significant difference between CLS and BLS arms (P=.85). During the 12 weeks of adaptive MyChart (Epic Systems) messaging, 18 (43%) CLS patients and 8 (21%) BLS patients performed daily self-weighing (P=.06), and 22 (52%) CLS patients and 14 (37%) BLS patients enrolled in referral-based lifestyle resources (P=.18).
Conclusions: Pragmatic enrollment, randomization, and data collection procedures proved feasible, and interventions showed preliminary effectiveness warranting further study in a larger trial.
{"title":"Hybrid Health IT and Telehealth-Delivered Behavioral Weight Loss Services for Primary Care Patients With Cardiovascular Risk Factors: Intervention Component Design and Pragmatic Randomized Feasibility Trial.","authors":"Ronald T Ackermann, Kenzie A Cameron, David T Liss, Nancy Dolan, Cassandra Aikman, Amy R Carson, Sterling A Harris, Kathryn Doyle, Andrew J Cooper, Brian Hitsman","doi":"10.2196/58722","DOIUrl":"10.2196/58722","url":null,"abstract":"<p><strong>Background: </strong>Intensive lifestyle interventions (ILI) improve weight loss and cardiovascular risk factors, but health care systems face challenges in implementing them. We engaged stakeholders to cocreate and evaluate primary care implementation strategies for ILI components.</p><p><strong>Objective: </strong>This study aimed to describe the design of intervention components and implementation strategies and to evaluate the feasibility of pragmatic trial enrollment and randomization procedures, as well as the acceptability and preliminary effectiveness of the interventions.</p><p><strong>Methods: </strong>The study setting was a single, urban primary care office. Patients with a BMI ≥27 kg/m² and ≥1 cardiovascular risk factor were sent a single electronic health record (EHR) message between December 2019 and January 2020 offering services to support a weight loss goal of 10 pounds in 10 weeks. All patients who affirmed interest were pragmatically enrolled in a trial offering basic lifestyle support (BLS), which provided a scale that transmits weight data to the EHR using cellular networks, a coupon to enroll in lifestyle coaching resources through a partnering fitness organization, and periodic EHR messages encouraging use of those resources. About half (n=42) of participants were randomized by an EHR algorithm to also receive customized lifestyle support (CLS), including weekly email messages adaptive to weight loss progress and telephonic coaching by a nurse for those facing challenges. Interventions and assessments spanned from January to July 2020, with disruption by the COVID-19 pandemic. Weight data were collected from administrative sources. Qualitative analysis of stakeholder recommendations and patient interviews assessed intervention acceptability, appropriateness, and sustainability.</p><p><strong>Results: </strong>Over 6 weeks, 426 patients were sent the EHR invitation message, and 80 (18.8%) patients affirmed interest in the weight loss goal and were enrolled. Overall, 48 of 80 (60%) trial participants lost weight at 6 months; 12 (15%) exhibited weight loss ≥5%, with no significant difference between CLS and BLS arms (P=.85). During the 12 weeks of adaptive MyChart (Epic Systems) messaging, 18 (43%) CLS patients and 8 (21%) BLS patients performed daily self-weighing (P=.06), and 22 (52%) CLS patients and 14 (37%) BLS patients enrolled in referral-based lifestyle resources (P=.18).</p><p><strong>Conclusions: </strong>Pragmatic enrollment, randomization, and data collection procedures proved feasible, and interventions showed preliminary effectiveness warranting further study in a larger trial.</p>","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":"13 ","pages":"e58722"},"PeriodicalIF":6.2,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12543212/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145345019","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Banchia Palmen, Zjala Ebadi, Maarten van Herck, Yvonne M J Goërtz, Qichen Deng, Melissa S Y Thong, Chris Burtin, Jeannette B Peters, Roy T M Sprooten, Erik W M A Bischoff, Emiel F M Wouters, Mirjam A G Sprangers, Jan H Vercoulen, Sarah Houben-Wilke, Anouk W Vaes, Daisy J A Janssen, Martijn A Spruit
Background: Questionnaire-based symptom assessment may introduce recall bias and lacks bidirectional exploration. This is particularly relevant, given the unclear direction of the associations between physical activity (PA), sedentary time (ST), and symptoms in patients with chronic obstructive pulmonary disease (COPD). Understanding these associations could inform symptom management strategies and improve patient quality of life.
Objective: This study aimed to investigate the direction of the association between PA, ST, and symptoms in patients with COPD using accelerometry and ecological momentary assessment (EMA).
Methods: A subsample from the FAntasTIGUE study answered 8 randomly timed EMA questionnaires daily for 5 days. Ten symptoms were rated on a 7-point Likert scale: "I feel relaxed, short of breath, energetic, cheerful, insecure, irritated, satisfied, anxious, tired, and mentally fit." Concurrently, step count and ST were measured using the ActiGraph GT9X Link placed on the right hip. Step count and ST 15 and 30 minutes pre- and post-EMA were used in multilevel models, controlled for pre-EMA steps and ST, and the previous EMA score. Significant confounders were used as covariates, and patient ID was used as random intercept.
Results: Thirty-four patients (19/34, 56% men, mean age 66, SD 7 years; forced expiratory volume in 1 second 52±20% predicted; 1035 EMA responses) were included. Feeling more relaxed was associated with a higher step count 15 minutes post-EMA (β=5.1; 95% CI 0.9 to 10.1; P=.046). Conversely, higher step count 15 and 30 minutes pre-EMA was associated with feeling less relaxed (β=-5.2×10-4; 95% CI -9.7×10-4 to -7.0×10-5; P=.02; and β=-3.2×10-4; 95% CI -5.6×10-4 to -7.9×10-5; P=.009), more short of breath (β=8.5×10-4; 95% CI 4.7×10-4 to 1.2×10-3; P<.001; and β=4.6×10-4; 95% CI 2.6×10-4 to 6.6×10-4; P<.001), and tired (β=5.1×10-4; 95% CI 7.2×10-5 to 9.4×10-4; P=.02; and β=2.9×10-4; 95% CI 5.3×10-5 to 5.2×10-4; P=.02). Higher ST 15 and 30 minutes pre-EMA was associated with feeling more anxious (β=1.7×10-4; 95% CI 1.7×10-5 to 3.2×10-4; P=.03; and β=8.5×10-5; 95% CI 2.5×10-6 to 1.7×10-4; P=.04).
Conclusions: A bidirectional association of feeling relaxed with PA was found in patients with COPD. Higher step count was related to feeling more short of breath and tired, whereas higher ST was associated with heightened anxiety.
背景:基于问卷的症状评估可能会引入回忆偏倚,缺乏双向探索。考虑到慢性阻塞性肺疾病(COPD)患者体力活动(PA)、久坐时间(ST)和症状之间的关联方向尚不明确,这一点尤为重要。了解这些关联可以为症状管理策略提供信息,并改善患者的生活质量。目的:本研究旨在通过加速计和生态瞬时评估(EMA)研究COPD患者PA、ST与症状之间的关系。方法:从FAntasTIGUE研究中抽取一个子样本,连续5天每天随机回答8份EMA问卷。10种症状按7分李克特量表打分:“我感到放松、呼吸急促、精力充沛、愉快、不安全、烦躁、满足、焦虑、疲倦和精神健康。”同时,使用放置在右臀部的ActiGraph GT9X Link测量步数和ST。在多水平模型中使用EMA前后15和30分钟的步数和ST,控制EMA前步数和ST,以及之前的EMA评分。采用显著混杂因素作为协变量,患者ID作为随机截距。结果:纳入34例患者(19/34,56%男性,平均年龄66,SD 7岁;1秒用力呼气量预测52±20%;EMA应答1035例)。感觉更放松与ema后15分钟较高的步数相关(β=5.1; 95% CI 0.9至10.1;P= 0.046)。相反,高15 - 30分钟pre-EMA步数与感觉不那么放松(β= -5.2 4×打败;95% CI -9.7 4×打败-7.0×纯;P = .02;和β= -3.2 4×打败;95% CI -5.6 4×打败-7.9×纯;P = .009),更多的呼吸急促(β= 8.5 4×打败;95% CI 4.7球季1.2×4×打败;PConclusions:双向关联的感觉放松与PA在COPD患者被发现。步数越高,感觉越气短和疲倦,而ST值越高,则越焦虑。
{"title":"Bidirectional Associations Between Physical Activity, Sedentary Behavior, and Daily Symptoms in Patients With Chronic Obstructive Pulmonary Disease: Longitudinal Observational Study.","authors":"Banchia Palmen, Zjala Ebadi, Maarten van Herck, Yvonne M J Goërtz, Qichen Deng, Melissa S Y Thong, Chris Burtin, Jeannette B Peters, Roy T M Sprooten, Erik W M A Bischoff, Emiel F M Wouters, Mirjam A G Sprangers, Jan H Vercoulen, Sarah Houben-Wilke, Anouk W Vaes, Daisy J A Janssen, Martijn A Spruit","doi":"10.2196/65653","DOIUrl":"10.2196/65653","url":null,"abstract":"<p><strong>Background: </strong>Questionnaire-based symptom assessment may introduce recall bias and lacks bidirectional exploration. This is particularly relevant, given the unclear direction of the associations between physical activity (PA), sedentary time (ST), and symptoms in patients with chronic obstructive pulmonary disease (COPD). Understanding these associations could inform symptom management strategies and improve patient quality of life.</p><p><strong>Objective: </strong>This study aimed to investigate the direction of the association between PA, ST, and symptoms in patients with COPD using accelerometry and ecological momentary assessment (EMA).</p><p><strong>Methods: </strong>A subsample from the FAntasTIGUE study answered 8 randomly timed EMA questionnaires daily for 5 days. Ten symptoms were rated on a 7-point Likert scale: \"I feel relaxed, short of breath, energetic, cheerful, insecure, irritated, satisfied, anxious, tired, and mentally fit.\" Concurrently, step count and ST were measured using the ActiGraph GT9X Link placed on the right hip. Step count and ST 15 and 30 minutes pre- and post-EMA were used in multilevel models, controlled for pre-EMA steps and ST, and the previous EMA score. Significant confounders were used as covariates, and patient ID was used as random intercept.</p><p><strong>Results: </strong>Thirty-four patients (19/34, 56% men, mean age 66, SD 7 years; forced expiratory volume in 1 second 52±20% predicted; 1035 EMA responses) were included. Feeling more relaxed was associated with a higher step count 15 minutes post-EMA (β=5.1; 95% CI 0.9 to 10.1; P=.046). Conversely, higher step count 15 and 30 minutes pre-EMA was associated with feeling less relaxed (β=-5.2×10-4; 95% CI -9.7×10-4 to -7.0×10-5; P=.02; and β=-3.2×10-4; 95% CI -5.6×10-4 to -7.9×10-5; P=.009), more short of breath (β=8.5×10-4; 95% CI 4.7×10-4 to 1.2×10-3; P<.001; and β=4.6×10-4; 95% CI 2.6×10-4 to 6.6×10-4; P<.001), and tired (β=5.1×10-4; 95% CI 7.2×10-5 to 9.4×10-4; P=.02; and β=2.9×10-4; 95% CI 5.3×10-5 to 5.2×10-4; P=.02). Higher ST 15 and 30 minutes pre-EMA was associated with feeling more anxious (β=1.7×10-4; 95% CI 1.7×10-5 to 3.2×10-4; P=.03; and β=8.5×10-5; 95% CI 2.5×10-6 to 1.7×10-4; P=.04).</p><p><strong>Conclusions: </strong>A bidirectional association of feeling relaxed with PA was found in patients with COPD. Higher step count was related to feeling more short of breath and tired, whereas higher ST was associated with heightened anxiety.</p>","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":"13 ","pages":"e65653"},"PeriodicalIF":6.2,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12543037/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145344972","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Cancer-related fatigue is a common and significant symptom experienced by patients with cancer and survivors across all age groups, profoundly impacting their quality of life. Adolescents and young adults often encounter substantial academic, career, and personal demands, which pose unique challenges in managing this symptom and may have a more profound overall impact on their lives. While digital health interventions show considerable promise in managing cancer-related fatigue, few reviews have specifically addressed their use among adolescents and young adults.
Objective: This scoping review aimed to identify and assess the types and effectiveness of digital health interventions in managing cancer-related fatigue among adolescents and young adults.
Methods: A comprehensive literature search was conducted using the keywords "digital health," "adolescent," "young adult," "fatigue," and "neoplasms" across 6 databases: PubMed, CINAHL, PsycINFO, Embase, Cochrane Library, and Web of Science. The search included English-language publications from the inception of each database to August 2024. Two researchers independently screened the studies based on predetermined inclusion and exclusion criteria.
Results: A total of 2965 articles were retrieved during the initial search, of which 10 (0.34%) satisfied the inclusion criteria of this review. The 10 included studies comprised 5 (50%) randomized controlled trials, 2 (20%) quasi-experimental studies, 2 (20%) mixed methods studies, and 1 (10%) cohort study. On the basis of the functions and forms of digital health interventions, the interventions included in this review were categorized into the following 5 types: dynamic health monitoring and feedback, automated online guidance and feedback, live remote coaching and instruction, gamified interventions, and robot-assisted interventions. Multiple studies (7/10, 70%) demonstrated that digital health interventions are effective in reducing cancer-related fatigue in adolescents and young adults and show potential in improving physical function and emotional well-being in this population.
Conclusions: Digital health interventions overcome the time and spatial limitations of traditional treatments and provide holistic support across physical, psychological, and social domains. They hold significant potential to alleviate cancer-related fatigue in adolescents and young adults. Future research should integrate various fatigue measurement scales and conduct large-scale studies and long-term follow-ups to capture a more comprehensive range of fatigue experiences, validate these findings, and enhance the effectiveness of digital health interventions.
背景:癌症相关疲劳是所有年龄段的癌症患者和幸存者都经历过的一种常见且重要的症状,深刻地影响着他们的生活质量。青少年和年轻人经常遇到大量的学术、事业和个人需求,这对管理这种症状构成了独特的挑战,并可能对他们的生活产生更深远的整体影响。虽然数字健康干预措施在管理与癌症相关的疲劳方面显示出相当大的希望,但很少有评论专门讨论它们在青少年和年轻人中的使用情况。目的:本综述旨在确定和评估数字健康干预措施在管理青少年和年轻人癌症相关疲劳方面的类型和有效性。方法:通过PubMed、CINAHL、PsycINFO、Embase、Cochrane Library和Web of Science等6个数据库,以“数字健康”、“青少年”、“年轻人”、“疲劳”和“肿瘤”等关键词进行全面的文献检索。搜索包括从每个数据库建立之初到2024年8月的英语出版物。两名研究人员根据预先确定的纳入和排除标准独立筛选研究。结果:初始检索共检索到2965篇文献,其中10篇(0.34%)符合本综述的纳入标准。纳入的10项研究包括5项(50%)随机对照试验、2项(20%)准实验研究、2项(20%)混合方法研究和1项(10%)队列研究。根据数字健康干预的功能和形式,本文将数字健康干预分为5类:动态健康监测与反馈、自动在线指导与反馈、实时远程指导与指导、游戏化干预和机器人辅助干预。多项研究(7/ 10,70 %)表明,数字健康干预措施可有效减少青少年和年轻人的癌症相关疲劳,并显示出改善这一人群身体功能和情绪健康的潜力。结论:数字卫生干预克服了传统治疗的时间和空间限制,并提供了跨越身体、心理和社会领域的整体支持。它们在缓解青少年和年轻人的癌症相关疲劳方面具有巨大的潜力。未来的研究应整合各种疲劳测量量表,进行大规模研究和长期随访,以获取更全面的疲劳体验,验证这些发现,并提高数字健康干预措施的有效性。
{"title":"Digital Health Interventions to Reduce Cancer-Related Fatigue Among Adolescents and Young Adults: Scoping Review.","authors":"Shanshan Jiang, Xiaoyu Yang, Xinying Yu","doi":"10.2196/68834","DOIUrl":"10.2196/68834","url":null,"abstract":"<p><strong>Background: </strong>Cancer-related fatigue is a common and significant symptom experienced by patients with cancer and survivors across all age groups, profoundly impacting their quality of life. Adolescents and young adults often encounter substantial academic, career, and personal demands, which pose unique challenges in managing this symptom and may have a more profound overall impact on their lives. While digital health interventions show considerable promise in managing cancer-related fatigue, few reviews have specifically addressed their use among adolescents and young adults.</p><p><strong>Objective: </strong>This scoping review aimed to identify and assess the types and effectiveness of digital health interventions in managing cancer-related fatigue among adolescents and young adults.</p><p><strong>Methods: </strong>A comprehensive literature search was conducted using the keywords \"digital health,\" \"adolescent,\" \"young adult,\" \"fatigue,\" and \"neoplasms\" across 6 databases: PubMed, CINAHL, PsycINFO, Embase, Cochrane Library, and Web of Science. The search included English-language publications from the inception of each database to August 2024. Two researchers independently screened the studies based on predetermined inclusion and exclusion criteria.</p><p><strong>Results: </strong>A total of 2965 articles were retrieved during the initial search, of which 10 (0.34%) satisfied the inclusion criteria of this review. The 10 included studies comprised 5 (50%) randomized controlled trials, 2 (20%) quasi-experimental studies, 2 (20%) mixed methods studies, and 1 (10%) cohort study. On the basis of the functions and forms of digital health interventions, the interventions included in this review were categorized into the following 5 types: dynamic health monitoring and feedback, automated online guidance and feedback, live remote coaching and instruction, gamified interventions, and robot-assisted interventions. Multiple studies (7/10, 70%) demonstrated that digital health interventions are effective in reducing cancer-related fatigue in adolescents and young adults and show potential in improving physical function and emotional well-being in this population.</p><p><strong>Conclusions: </strong>Digital health interventions overcome the time and spatial limitations of traditional treatments and provide holistic support across physical, psychological, and social domains. They hold significant potential to alleviate cancer-related fatigue in adolescents and young adults. Future research should integrate various fatigue measurement scales and conduct large-scale studies and long-term follow-ups to capture a more comprehensive range of fatigue experiences, validate these findings, and enhance the effectiveness of digital health interventions.</p>","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":"13 ","pages":"e68834"},"PeriodicalIF":6.2,"publicationDate":"2025-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12539328/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145337123","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Higinio Fernández-Sánchez, Javier Salazar-Alberto, Jhan Carlos Manuel Fernandez-Delgado, Annalynn Galvin, Michael J Mugavero, Carlos E Rodriguez-Diaz, Diane Santa Maria
<p><strong>Background: </strong>Canada, Mexico, and the United States are primary transit destinations for migrants in the Western Hemisphere. Migrants face barriers to accessing health services, including HIV/AIDS and STI prevention. Mobile apps may enhance public health access for these populations.</p><p><strong>Objective: </strong>This study systematically identifies and evaluates mobile apps supporting HIV and STI prevention in Canada, Mexico, and the United States.</p><p><strong>Methods: </strong>An environmental scan of 357 mobile applications from the Google Play and Apple App stores was conducted on June 18, 2024, following the rigorous six-step framework proposed by Fernández-Sánchez to ensure a systematic and comprehensive evaluation of apps for HIV and STI prevention. Predefined inclusion and exclusion criteria were applied, resulting in 6 eligible apps. Each app was assessed using the 29-item Mobile App Rating Scale (MARS), scored on a 5-point Likert scale (1 = inadequate, 5 = excellent), and categorized as high (3), medium (2), or low (1) based on mean scores. Internal consistency was excellent (Cronbach's α = 0.90), and inter-rater reliability demonstrated near-perfect agreement (Cohen's κ = 0.862). Data analysis was performed using SPSS version 27.</p><p><strong>Results: </strong>All six apps were available in Canada, Mexico, and the United States, with 33.3% from Google Play, 16.7% from Apple, and 50.0% from both platforms. MARS evaluation revealed high quality ratings for Engagement (100%), Functionality (88.9%), Aesthetics (83.3%), and Interaction (83.0%), as well as high subjective quality (83.3%) and app-specific quality (88.9%). Life4Me+ was the highest-rated app (4.6; 3/5), while HIV-TEST received the lowest rating (3.4; 7/5). Most apps (83.3%) were only available in English, and 16.7% supported multiple languages, which may limit accessibility for non-English-speaking migrant populations. Additionally, 83.3% were updated in 2024, 33.3% were linked to non-governmental organization, 16.7% to a university, and 50.0% had no clear affiliation. Regarding their focus, 50.0% addressed STI prevention, diagnosis, and treatment, 16.7% combined HIV and STI prevention, and 33.3% provided PrEP-related resources.</p><p><strong>Conclusions: </strong>These six apps stand out for their high functionality, engagement, and accessibility, establishing themselves as effective tools for HIV and STI prevention education among migrant populations. This study highlights the critical role of digital resources in addressing public health challenges faced by vulnerable and minority groups. Integrating these apps into health promotion strategies is essential to improve health literacy and encourage preventive behaviors. Moreover, ensuring the quality, credibility, linguistic diversity, and continuous updating of these digital interventions is crucial to achieving a real and sustained impact on public health. Policies should promote clear standards that
{"title":"Mobile Apps for HIV and STI Prevention in Canada, Mexico, and the United States: An Environmental Scan.","authors":"Higinio Fernández-Sánchez, Javier Salazar-Alberto, Jhan Carlos Manuel Fernandez-Delgado, Annalynn Galvin, Michael J Mugavero, Carlos E Rodriguez-Diaz, Diane Santa Maria","doi":"10.2196/72009","DOIUrl":"10.2196/72009","url":null,"abstract":"<p><strong>Background: </strong>Canada, Mexico, and the United States are primary transit destinations for migrants in the Western Hemisphere. Migrants face barriers to accessing health services, including HIV/AIDS and STI prevention. Mobile apps may enhance public health access for these populations.</p><p><strong>Objective: </strong>This study systematically identifies and evaluates mobile apps supporting HIV and STI prevention in Canada, Mexico, and the United States.</p><p><strong>Methods: </strong>An environmental scan of 357 mobile applications from the Google Play and Apple App stores was conducted on June 18, 2024, following the rigorous six-step framework proposed by Fernández-Sánchez to ensure a systematic and comprehensive evaluation of apps for HIV and STI prevention. Predefined inclusion and exclusion criteria were applied, resulting in 6 eligible apps. Each app was assessed using the 29-item Mobile App Rating Scale (MARS), scored on a 5-point Likert scale (1 = inadequate, 5 = excellent), and categorized as high (3), medium (2), or low (1) based on mean scores. Internal consistency was excellent (Cronbach's α = 0.90), and inter-rater reliability demonstrated near-perfect agreement (Cohen's κ = 0.862). Data analysis was performed using SPSS version 27.</p><p><strong>Results: </strong>All six apps were available in Canada, Mexico, and the United States, with 33.3% from Google Play, 16.7% from Apple, and 50.0% from both platforms. MARS evaluation revealed high quality ratings for Engagement (100%), Functionality (88.9%), Aesthetics (83.3%), and Interaction (83.0%), as well as high subjective quality (83.3%) and app-specific quality (88.9%). Life4Me+ was the highest-rated app (4.6; 3/5), while HIV-TEST received the lowest rating (3.4; 7/5). Most apps (83.3%) were only available in English, and 16.7% supported multiple languages, which may limit accessibility for non-English-speaking migrant populations. Additionally, 83.3% were updated in 2024, 33.3% were linked to non-governmental organization, 16.7% to a university, and 50.0% had no clear affiliation. Regarding their focus, 50.0% addressed STI prevention, diagnosis, and treatment, 16.7% combined HIV and STI prevention, and 33.3% provided PrEP-related resources.</p><p><strong>Conclusions: </strong>These six apps stand out for their high functionality, engagement, and accessibility, establishing themselves as effective tools for HIV and STI prevention education among migrant populations. This study highlights the critical role of digital resources in addressing public health challenges faced by vulnerable and minority groups. Integrating these apps into health promotion strategies is essential to improve health literacy and encourage preventive behaviors. Moreover, ensuring the quality, credibility, linguistic diversity, and continuous updating of these digital interventions is crucial to achieving a real and sustained impact on public health. Policies should promote clear standards that","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":" ","pages":""},"PeriodicalIF":6.2,"publicationDate":"2025-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145337147","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sanghee Lee, Chan Yoon, Chi-Hyun Choi, Tae Hyun Park, Sang Jin Yang, Ha Ri Cha, Tae Woo Kim, Jae Hyeon Park, Moon Jong Chang, Chong Bum Chang
<p><strong>Background: </strong>Patellofemoral pain (PFP) is a common musculoskeletal disorder characterized by persistent knee pain, often without any structural abnormalities. Conservative treatments, particularly exercise therapy, are widely recommended; however, adherence remains generally low, and full recovery is often not achieved. Psychological interventions can aid in symptom management; however, studies integrating cognitive behavioral therapy (CBT), which is known to be effective for chronic pain, with exercise therapy for patients with PFP are limited. This study examined the impact of MORA Cure (PFP), a multidisciplinary digital therapeutics (DTx) app that integrates exercise and CBT, in comparison with conventional treatments for PFP management.</p><p><strong>Objective: </strong>This study aimed to evaluate the efficacy and safety of an 8-week DTx intervention incorporating exercise and CBT compared with in-person exercise education in patients with PFP.</p><p><strong>Methods: </strong>A parallel-group randomized controlled trial was conducted with 35 patients diagnosed with PFP recruited from orthopedic outpatient clinics. Participants were randomly assigned to either the DTx group (n=18, 51%) or the control group (n=17, 49%). The DTx group received an 8-week intervention via the MORA Cure (PFP) app incorporating home-based exercises and weekly CBT modules with daily worksheets. The control group received conventional treatment, including disease education, a single in-person exercise education session conducted by a medical professional, and encouragement to continue self-exercising throughout the study period. The outcome measures included pain severity (usual and worst, assessed using the numeric pain rating scale), functional disability (Anterior Knee Pain Scale), knee extension strength (measured using an isokinetic dynamometer), health-related quality of life (EQ-5D), and mental health status (9-item Patient Health Questionnaire). Assessments were conducted from baseline at 4-week intervals for up to 12 weeks.</p><p><strong>Results: </strong>The DTx group showed significant reductions in usual pain at each time point (4 weeks: mean score 2.2, SD 1.5, and P=.006; 8 weeks: mean 2.3, SD 1.7, and P=.003; 12 weeks: mean 1.2, SD 1.8, and P=.008), whereas the control group exhibited no changes. The knee extension strength in the DTx group increased significantly at both 8 and 12 weeks (P<.001), with greater improvement than that in the control group at 8 weeks (P=.04). Both groups showed significant improvements in functional disability at 12 weeks (DTx: mean score 85.2, SD 12.7, and P=.006; control: mean 84.5, SD 13.0, and P=.01). Health-related quality of life (EQ-5D) also improved in the DTx group at 8 and 12 weeks, whereas the control group showed improvement only at 12 weeks.</p><p><strong>Conclusions: </strong>This multidisciplinary DTx intervention was associated with significant pain reduction, improved functional disability
{"title":"Efficacy of a Mobile Multidisciplinary Digital Therapeutics App for Patellofemoral Pain: Randomized Controlled Trial.","authors":"Sanghee Lee, Chan Yoon, Chi-Hyun Choi, Tae Hyun Park, Sang Jin Yang, Ha Ri Cha, Tae Woo Kim, Jae Hyeon Park, Moon Jong Chang, Chong Bum Chang","doi":"10.2196/69627","DOIUrl":"10.2196/69627","url":null,"abstract":"<p><strong>Background: </strong>Patellofemoral pain (PFP) is a common musculoskeletal disorder characterized by persistent knee pain, often without any structural abnormalities. Conservative treatments, particularly exercise therapy, are widely recommended; however, adherence remains generally low, and full recovery is often not achieved. Psychological interventions can aid in symptom management; however, studies integrating cognitive behavioral therapy (CBT), which is known to be effective for chronic pain, with exercise therapy for patients with PFP are limited. This study examined the impact of MORA Cure (PFP), a multidisciplinary digital therapeutics (DTx) app that integrates exercise and CBT, in comparison with conventional treatments for PFP management.</p><p><strong>Objective: </strong>This study aimed to evaluate the efficacy and safety of an 8-week DTx intervention incorporating exercise and CBT compared with in-person exercise education in patients with PFP.</p><p><strong>Methods: </strong>A parallel-group randomized controlled trial was conducted with 35 patients diagnosed with PFP recruited from orthopedic outpatient clinics. Participants were randomly assigned to either the DTx group (n=18, 51%) or the control group (n=17, 49%). The DTx group received an 8-week intervention via the MORA Cure (PFP) app incorporating home-based exercises and weekly CBT modules with daily worksheets. The control group received conventional treatment, including disease education, a single in-person exercise education session conducted by a medical professional, and encouragement to continue self-exercising throughout the study period. The outcome measures included pain severity (usual and worst, assessed using the numeric pain rating scale), functional disability (Anterior Knee Pain Scale), knee extension strength (measured using an isokinetic dynamometer), health-related quality of life (EQ-5D), and mental health status (9-item Patient Health Questionnaire). Assessments were conducted from baseline at 4-week intervals for up to 12 weeks.</p><p><strong>Results: </strong>The DTx group showed significant reductions in usual pain at each time point (4 weeks: mean score 2.2, SD 1.5, and P=.006; 8 weeks: mean 2.3, SD 1.7, and P=.003; 12 weeks: mean 1.2, SD 1.8, and P=.008), whereas the control group exhibited no changes. The knee extension strength in the DTx group increased significantly at both 8 and 12 weeks (P<.001), with greater improvement than that in the control group at 8 weeks (P=.04). Both groups showed significant improvements in functional disability at 12 weeks (DTx: mean score 85.2, SD 12.7, and P=.006; control: mean 84.5, SD 13.0, and P=.01). Health-related quality of life (EQ-5D) also improved in the DTx group at 8 and 12 weeks, whereas the control group showed improvement only at 12 weeks.</p><p><strong>Conclusions: </strong>This multidisciplinary DTx intervention was associated with significant pain reduction, improved functional disability","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":"13 ","pages":"e69627"},"PeriodicalIF":6.2,"publicationDate":"2025-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12579297/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145312846","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nora Jacobson, Linda S Park, Alice Pulvermacher, Samantha Voelker, Mallory Herzog, Andrew Quanbeck
Background: Implementation frameworks such as the Exploration, Preparation, Implementation, Sustainment model emphasize the importance of the fit between an intervention and its context, which includes the needs of its target population, as well as the culture, resources, and capabilities of the implementing organization. Although lack of fit is a major barrier to implementation, fit has not often been a focus of implementation research. This paper uses fit as a lens to examine the implementation of Tula, a mobile health app aimed at reducing risky drinking days among individuals meeting the criteria for mild to moderate alcohol use disorder, in a 3-arm (app alone, app plus peer mentoring, and app plus health coaching) randomized controlled trial.
Objective: We sought to better understand the trial results and to provide actionable guidance for future implementation of digital health interventions in health care organizations.
Methods: Semistructured interviews with 18 trial participants and 7 Tula implementers were conducted. Trial participants were pulled equally from each arm of the trial and represented participants who demonstrated both high and low engagement with the app. Implementers consisted of a project manager, 4 peer mentors, and 2 health coaches. Interviews with participants focused on their motivations, opinions, and experiences of the intervention and their perception of their drinking behavior following the intervention, including how their use of the app worked to change that behavior. Interviews with implementers were centered on their roles, theories of change, perceptions of intervention, and areas for improvement. All interviews were analyzed using rapid qualitative analysis with deductive and inductive components.
Results: We identified areas of both fit and misfit. For example, there was a good fit between implementers' theories of change and participants' description of how change occurred. Fit was improved by the versatility of the app, which allowed participants to customize their experiences. Conversely, misfit was noted in the app's inability to cultivate connection for many participants and a disjunction between the role of peer mentors in the intervention and their broader professional ethos.
Conclusions: Focusing on fit provides a useful guide to enhance future iterations of the Tula app that lead to better sustainment of the intervention.
{"title":"Exploring Fit in a Mobile Health Intervention for Alcohol Use Disorder: Qualitative Study.","authors":"Nora Jacobson, Linda S Park, Alice Pulvermacher, Samantha Voelker, Mallory Herzog, Andrew Quanbeck","doi":"10.2196/65218","DOIUrl":"10.2196/65218","url":null,"abstract":"<p><strong>Background: </strong>Implementation frameworks such as the Exploration, Preparation, Implementation, Sustainment model emphasize the importance of the fit between an intervention and its context, which includes the needs of its target population, as well as the culture, resources, and capabilities of the implementing organization. Although lack of fit is a major barrier to implementation, fit has not often been a focus of implementation research. This paper uses fit as a lens to examine the implementation of Tula, a mobile health app aimed at reducing risky drinking days among individuals meeting the criteria for mild to moderate alcohol use disorder, in a 3-arm (app alone, app plus peer mentoring, and app plus health coaching) randomized controlled trial.</p><p><strong>Objective: </strong>We sought to better understand the trial results and to provide actionable guidance for future implementation of digital health interventions in health care organizations.</p><p><strong>Methods: </strong>Semistructured interviews with 18 trial participants and 7 Tula implementers were conducted. Trial participants were pulled equally from each arm of the trial and represented participants who demonstrated both high and low engagement with the app. Implementers consisted of a project manager, 4 peer mentors, and 2 health coaches. Interviews with participants focused on their motivations, opinions, and experiences of the intervention and their perception of their drinking behavior following the intervention, including how their use of the app worked to change that behavior. Interviews with implementers were centered on their roles, theories of change, perceptions of intervention, and areas for improvement. All interviews were analyzed using rapid qualitative analysis with deductive and inductive components.</p><p><strong>Results: </strong>We identified areas of both fit and misfit. For example, there was a good fit between implementers' theories of change and participants' description of how change occurred. Fit was improved by the versatility of the app, which allowed participants to customize their experiences. Conversely, misfit was noted in the app's inability to cultivate connection for many participants and a disjunction between the role of peer mentors in the intervention and their broader professional ethos.</p><p><strong>Conclusions: </strong>Focusing on fit provides a useful guide to enhance future iterations of the Tula app that lead to better sustainment of the intervention.</p>","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":"13 ","pages":"e65218"},"PeriodicalIF":6.2,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12605291/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145292230","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
<p><strong>Background: </strong>Drug-drug interactions (DDIs) pose a significant risk to patient safety and increase health care costs. Mobile apps offer potential solutions for managing DDIs, yet their quality and effectiveness from the user's perspective remain unclear.</p><p><strong>Objective: </strong>The aim is to evaluate the quality of publicly available mobile apps for DDI management in the US using the Mobile App Rating Scale (MARS) and to identify patterns that reflect user satisfaction and preferences.</p><p><strong>Methods: </strong>A structured review was conducted to identify mobile apps for DDI management, resulting in 19 eligible apps. Two health care-affiliated evaluators independently assessed each app using the mobile app rating scale (MARS). Dimensionality scores were calculated, and correlation analysis was conducted to examine relationships among dimensions. K-means clustering was applied to group apps based on their MARS scores. Scatter plots visualized app distributions across clusters. To validate the clustering model and assess alignment with user satisfaction, mean weighted user ratings were compared with mean MARS scores per cluster. Correlation analysis was also performed between individual MARS dimensions and user ratings within each cluster.</p><p><strong>Results: </strong>The mean MARS score was 3.54 out of 5, with the Information dimension scoring the highest (mean 3.68, SD 0.51) and Engagement the lowest (mean 3.42, SD 0.80). The Kruskal-Wallis test revealed no significant differences in median scores across the four dimensions (χ²3=2.109, P=.55). All MARS dimensions were positively correlated (r=0.65 to 0.92), indicating interrelated quality characteristics. K-means clustering identified three app groups with varying quality profiles: Cluster 1 (n=7, mean MARS=2.86), Cluster 2 (n=7, mean=3.57), and Cluster 3 (n=5, mean=4.44). Cluster 1 apps showed strongest correlations between user satisfaction and functionality (r=0.74) and engagement (r=0.53). Cluster 2 users prioritized information (r=0.41) and aesthetics (r=0.58), and Cluster 3 exhibited balanced influence from information (r=0.62), aesthetics (r=0.58), and functionality (r=0.39). Scatter plots indicated that engagement, functionality, and aesthetics were key drivers of user perception, while information, though consistently strong, played a lesser role in differentiating the apps. The weighted user ratings aligned with MARS scores, supporting the validity of the clustering model.</p><p><strong>Conclusions: </strong>This study assesses the quality of mobile apps for DDI management by integrating MARS with K-means Clustering. This approach enabled a structured classification of apps based on the MARS scores, identifying distinct clusters that reflect overall app quality profiles across key usability dimensions. The study revealed that the influence of MARS dimensions on app ratings varies by cluster, highlighting that the significance of these dimensions shi
{"title":"Investigating the Quality of Mobile Apps for Drug-Drug Interaction Management Using the Mobile App Rating Scale and K-Means Clustering: Systematic Search of App Stores.","authors":"Ayush Bhattacharya, Jose Fernando Florez-Arango","doi":"10.2196/65927","DOIUrl":"10.2196/65927","url":null,"abstract":"<p><strong>Background: </strong>Drug-drug interactions (DDIs) pose a significant risk to patient safety and increase health care costs. Mobile apps offer potential solutions for managing DDIs, yet their quality and effectiveness from the user's perspective remain unclear.</p><p><strong>Objective: </strong>The aim is to evaluate the quality of publicly available mobile apps for DDI management in the US using the Mobile App Rating Scale (MARS) and to identify patterns that reflect user satisfaction and preferences.</p><p><strong>Methods: </strong>A structured review was conducted to identify mobile apps for DDI management, resulting in 19 eligible apps. Two health care-affiliated evaluators independently assessed each app using the mobile app rating scale (MARS). Dimensionality scores were calculated, and correlation analysis was conducted to examine relationships among dimensions. K-means clustering was applied to group apps based on their MARS scores. Scatter plots visualized app distributions across clusters. To validate the clustering model and assess alignment with user satisfaction, mean weighted user ratings were compared with mean MARS scores per cluster. Correlation analysis was also performed between individual MARS dimensions and user ratings within each cluster.</p><p><strong>Results: </strong>The mean MARS score was 3.54 out of 5, with the Information dimension scoring the highest (mean 3.68, SD 0.51) and Engagement the lowest (mean 3.42, SD 0.80). The Kruskal-Wallis test revealed no significant differences in median scores across the four dimensions (χ²3=2.109, P=.55). All MARS dimensions were positively correlated (r=0.65 to 0.92), indicating interrelated quality characteristics. K-means clustering identified three app groups with varying quality profiles: Cluster 1 (n=7, mean MARS=2.86), Cluster 2 (n=7, mean=3.57), and Cluster 3 (n=5, mean=4.44). Cluster 1 apps showed strongest correlations between user satisfaction and functionality (r=0.74) and engagement (r=0.53). Cluster 2 users prioritized information (r=0.41) and aesthetics (r=0.58), and Cluster 3 exhibited balanced influence from information (r=0.62), aesthetics (r=0.58), and functionality (r=0.39). Scatter plots indicated that engagement, functionality, and aesthetics were key drivers of user perception, while information, though consistently strong, played a lesser role in differentiating the apps. The weighted user ratings aligned with MARS scores, supporting the validity of the clustering model.</p><p><strong>Conclusions: </strong>This study assesses the quality of mobile apps for DDI management by integrating MARS with K-means Clustering. This approach enabled a structured classification of apps based on the MARS scores, identifying distinct clusters that reflect overall app quality profiles across key usability dimensions. The study revealed that the influence of MARS dimensions on app ratings varies by cluster, highlighting that the significance of these dimensions shi","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":"13 ","pages":"e65927"},"PeriodicalIF":6.2,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12516926/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145280264","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}