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Benefits of Remote-Based Mindfulness on Physical Symptom Outcomes in Cancer Survivors: Systematic Review and Meta-Analysis.
IF 3.3 Q2 ONCOLOGY Pub Date : 2025-01-16 DOI: 10.2196/54154
Maria Komariah, Sidik Maulana, Shakira Amirah, Hesti Platini, Laili Rahayuwati, Ah Yusuf, Mohd Khairul Zul Hasymi Firdaus

Background: Many cancer survivors experience a wide range of symptoms closely linked to psychological problems, highlighting the need for psychological treatment, one of the most popular being mindfulness. The use of the internet has greatly increased in the last decade, and has encouraged the use of remote-based interventions to help people living with cancer access treatment remotely via devices.

Objective: The primary aim of this study was to explore the efficacy of internet-based mindfulness interventions on the physical symptoms of people living with cancer, where physical symptoms are defined as distressing somatic experiences (eg fatigue, insomnia, and pain) regardless of the underlying cause. The secondary aim was to investigate interventions for the quality of life (QoL).

Methods: This study followed the Preferred Reporting Items for Systematic Review and Meta-analysis (PRISMA) guidelines. Relevant articles were systematically searched using electronic databases, namely Scopus, Medline through PubMed, Cumulated Index in Nursing and Allied Health Literature (CINAHL) through EBSCOhost, and Cochrane Central Database. Randomized controlled and pilot trials involving adults and/or older adults with cancer and using remote-based mindfulness interventions compared to usual care were included. The quality of the trials included in this study was assessed using the revised Cochrane risk of bias, version 2.0. This study estimated the standardized mean difference (SMD) and mean difference (MD) with 95% CI. The I2 test was used to identify potential causes of heterogeneity. Publication bias was assessed using contour-enhanced funnel plots and the Egger linear regression test to reveal a small study effect.

Results: The initial search yielded 1985 records, of which 13 studies were ultimately included. After treatment, remote-based mindfulness significantly reduced fatigue (SMD -0.94; 95% CI: -1.56 to -0.33; P=.002), sleep disturbance (SMD -0.36; 95% CI: -0.60 to -0.12; P=.004), and improved physical function (SMD .25; 95% CI: 0.09 to 0.41; P=.002) compared to that observed before treatment. However, compared with usual care, remote-based mindfulness showed a statistically significant reduction only in sleep disturbance (SMD: -0.37; 95% CI: -0.58 to -0.16; P=.0006) after treatment. Moreover, remote-based mindfulness was not statistically significant in reducing pain both within and between groups.

Conclusions: Remote-based mindfulness shows promise in reducing sleep disturbances; however, its impact on fatigue, pain, and physical function may be limited.

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引用次数: 0
Analyzing Geospatial and Socioeconomic Disparities in Breast Cancer Screening Among Populations in the United States: Machine Learning Approach. 分析美国人群中乳腺癌筛查的地理空间和社会经济差异:机器学习方法。
IF 3.3 Q2 ONCOLOGY Pub Date : 2025-01-16 DOI: 10.2196/59882
Soheil Hashtarkhani, Yiwang Zhou, Fekede Asefa Kumsa, Shelley White-Means, David L Schwartz, Arash Shaban-Nejad

Background: Breast cancer screening plays a pivotal role in early detection and subsequent effective management of the disease, impacting patient outcomes and survival rates.

Objective: This study aims to assess breast cancer screening rates nationwide in the United States and investigate the impact of social determinants of health on these screening rates.

Methods: Data on mammography screening at the census tract level for 2018 and 2020 were collected from the Behavioral Risk Factor Surveillance System. We developed a large-scale dataset of social determinants of health, comprising 13 variables for 72,337 census tracts. Spatial analysis employing Getis-Ord Gi statistics was used to identify clusters of high and low breast cancer screening rates. To evaluate the influence of these social determinants, we implemented a random forest model, with the aim of comparing its performance to linear regression and support vector machine models. The models were evaluated using R2 and root mean squared error metrics. Shapley Additive Explanations values were subsequently used to assess the significance of variables and direction of their influence.

Results: Geospatial analysis revealed elevated screening rates in the eastern and northern United States, while central and midwestern regions exhibited lower rates. The random forest model demonstrated superior performance, with an R2=64.53 and root mean squared error of 2.06, compared to linear regression and support vector machine models. Shapley Additive Explanations values indicated that the percentage of the Black population, the number of mammography facilities within a 10-mile radius, and the percentage of the population with at least a bachelor's degree were the most influential variables, all positively associated with mammography screening rates.

Conclusions: These findings underscore the significance of social determinants and the accessibility of mammography services in explaining the variability of breast cancer screening rates in the United States, emphasizing the need for targeted policy interventions in areas with relatively lower screening rates.

背景:乳腺癌筛查在疾病的早期发现和随后的有效管理中起着关键作用,影响患者的预后和生存率。目的:本研究旨在评估美国全国乳腺癌筛查率,并调查健康的社会决定因素对这些筛查率的影响。方法:从行为危险因素监测系统中收集2018年和2020年普查区乳腺x线检查数据。我们开发了一个大规模的健康社会决定因素数据集,包括72,337个人口普查区的13个变量。采用Getis-Ord Gi统计数据进行空间分析,以确定乳腺癌筛查率高和低的群集。为了评估这些社会决定因素的影响,我们实施了一个随机森林模型,目的是将其性能与线性回归和支持向量机模型进行比较。使用R2和均方根误差指标对模型进行评估。随后使用沙普利加性解释值来评估变量的重要性及其影响的方向。结果:地理空间分析显示,美国东部和北部的筛查率较高,而中部和中西部地区的筛查率较低。与线性回归和支持向量机模型相比,随机森林模型表现出更好的性能,R2=64.53,均方根误差为2.06。Shapley加性解释值表明,黑人人口的百分比、10英里半径内乳房x光检查设施的数量以及至少拥有学士学位的人口的百分比是最具影响力的变量,它们都与乳房x光检查率呈正相关。结论:这些发现强调了社会决定因素和乳房x光检查服务的可及性在解释美国乳腺癌筛查率差异方面的重要性,强调了筛查率相对较低地区有针对性政策干预的必要性。
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引用次数: 0
Preliminary Effectiveness of a Telehealth-Delivered Exercise Program in Older Adults Living With and Beyond Cancer: Retrospective Study. 远程健康运动项目对老年癌症患者的初步效果:回顾性研究。
IF 3.3 Q2 ONCOLOGY Pub Date : 2025-01-13 DOI: 10.2196/56718
Emily R Dunston, Sonal Oza, Yang Bai, Maria Newton, Leslie Podlog, Kish Larson, Darren Walker, Rebecca W Zingg, Pamela A Hansen, Adriana M Coletta

Background: Exercise can attenuate the deleterious combined effects of cancer treatment and aging among older adults with cancer, yet exercise participation is low. Telehealth exercise may improve exercise engagement by decreasing time and transportation barriers; however, the utility of telehealth exercise among older adults with cancer is not well established.

Objective: We aimed to evaluate the preliminary effectiveness of a one-on-one, supervised telehealth exercise program on physical function, muscular endurance, balance, and flexibility among older adults with cancer.

Methods: In this retrospective study, we analyzed electronic health record data collected from the Personal Optimism With Exercise Recovery clinical exercise program delivered via telehealth among older adults with cancer (≥65 y) who completed a virtual initial program telehealth assessment between March 2020 and December 2021. The virtual initial assessment included the following measures: 30-second chair stand test, 30-second maximum push-up test, 2-minute standing march, single leg stance, plank, chair sit and reach, shoulder range of motion, and the clock test. All baseline measures were repeated after 12-weeks of telehealth exercise. Change scores were calculated for all assessments and compared to minimal clinically important difference (MCID) values for assessments with published MCIDs. Paired samples t tests (2-tailed) were conducted to determine change in assessment outcomes.

Results: Older adults with cancer who chose to participate in the telehealth exercise program (N=68) were 71.8 (SD 5.3) years of age on average (range 65-92 y). The 3 most common cancer types in this sample were breast (n=13), prostate (n=13), and multiple myeloma (n=8). All cancer stages were represented in this sample with stage II (n=16, 23.5%) and III (n=18, 26.5%) being the most common. A follow-up telehealth assessment was completed by 29.4% (n=20) of older adults with cancer. Among those who completed a follow-up telehealth assessment, there were significant increases in the 30-second chair stand (n=19; mean change +2.00 repetitions, 95% CI 0.12 to 3.88) and 30-second maximum push-up scores (n=20; mean change +2.85 repetitions, 95% CI 1.60 to 4.11). There were no significant differences for the 2-minute standing march, plank, single leg stance, sit and reach, shoulder mobility, or clock test (P>.05). Nine (47.3%) older adults with cancer had a change in 30-second chair stand scores greater than the MCID of 2 repetitions.

Conclusions: Our findings suggest a one-on-one, supervised telehealth exercise program may positively influence measures of physical function, muscular endurance, balance, and flexibility among older adults with cancer, but more adequately powered trials are needed to confirm these findings.

背景:在老年癌症患者中,运动可以减弱癌症治疗和衰老的有害综合效应,但运动参与率很低。远程保健练习可以通过减少时间和交通障碍来提高锻炼的参与度;然而,远程保健运动在老年癌症患者中的效用尚未得到很好的证实。目的:我们旨在评估一个一对一的、有监督的远程医疗锻炼计划对老年癌症患者身体功能、肌肉耐力、平衡和灵活性的初步效果。方法:在这项回顾性研究中,我们分析了通过远程医疗提供的个人乐观运动恢复临床运动计划收集的电子健康记录数据,这些数据来自于2020年3月至2021年12月期间完成虚拟初始计划远程医疗评估的老年癌症患者(≥65岁)。虚拟初始评估包括以下措施:30秒椅子站立测试,30秒最大俯卧撑测试,2分钟站立行军,单腿站立,平板支撑,椅子坐和伸展,肩部活动范围和时钟测试。所有基线测量在12周的远程医疗锻炼后重复进行。计算所有评估的变化评分,并与已公布的最小临床重要差异(MCID)值进行比较。进行配对样本t检验(双尾)以确定评估结果的变化。结果:选择参加远程医疗锻炼计划的老年癌症患者(N=68)平均年龄为71.8岁(SD = 5.3)(范围为65-92岁)。该样本中最常见的3种癌症类型是乳腺癌(N= 13)、前列腺癌(N= 13)和多发性骨髓瘤(N= 8)。在该样本中,所有癌症阶段都有代表,其中II期(n=16, 23.5%)和III期(n=18, 26.5%)最常见。29.4% (n=20)的老年癌症患者完成了随访远程健康评估。在完成后续远程医疗评估的人中,30秒站立椅的时间显著增加(n=19;平均变化+2.00次重复,95% CI 0.12至3.88)和30秒最大俯卧撑分数(n=20;平均变化+2.85个重复,95% CI 1.60 ~ 4.11)。2分钟站立行军、平板支撑、单腿站立、坐伸、肩部活动度或时钟测试无显著差异(P < 0.05)。9名(47.3%)老年癌症患者的30秒椅子站立得分变化大于2次重复的MCID。结论:我们的研究结果表明,一对一的、有监督的远程医疗锻炼计划可能对老年癌症患者的身体功能、肌肉耐力、平衡和灵活性的测量产生积极影响,但需要更充分有力的试验来证实这些发现。
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引用次数: 0
Design and Use of Patient-Facing Electronic Patient-Reported Outcomes and Sensor Data Visualizations During Outpatient Chemotherapy. 在门诊化疗期间设计和使用面向患者的电子患者报告结果和传感器数据可视化。
IF 3.3 Q2 ONCOLOGY Pub Date : 2025-01-10 DOI: 10.2196/62711
Christianna Bartel, Leeann Chen, Weiyu Huang, Qichang Li, Qingyang Li, Jennifer Fedor, Krina C Durica, Carissa A Low

Unlabelled: This study describes patients' interaction with a personalized web-based visualization displaying daily electronic patient-reported outcomes and wearable device data during outpatient chemotherapy.

无标签:本研究描述了患者在门诊化疗期间与个性化的基于网络的可视化交互,显示每日电子患者报告的结果和可穿戴设备数据。
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引用次数: 0
A Novel Telehealth Exercise Program Designed for Rural Survivors of Cancer With Cancer-Related Fatigue: Single-Arm Feasibility Trial. 为农村癌症相关疲劳幸存者设计的新型远程医疗锻炼方案:单组可行性试验。
IF 3.3 Q2 ONCOLOGY Pub Date : 2025-01-10 DOI: 10.2196/59478
Ryan J Marker, Andrew J Kittelson, Jared J Scorsone, Ian A Moran, John C Quindry, Heather J Leach
<p><strong>Background: </strong>Exercise interventions are among the best-known interventions for cancer-related fatigue (CRF). Rural survivors of cancer, however, report specific barriers to engaging in exercise programs and lack overall access to effective programs.</p><p><strong>Objective: </strong>The purpose of this investigation was to assess the feasibility of a novel telehealth exercise program designed specifically for rural survivors of cancer with CRF.</p><p><strong>Methods: </strong>A single-arm clinical trial of the BfitBwell Telehealth Program was performed. Based on an established clinical program, this adapted 12-week program addressed barriers previously reported by rural survivors by providing synchronous videoconference exercise sessions (2 per program), asynchronous exercise sessions using a personal training smartphone or internet app (3-5 per week), and regular symptom (CRF) monitoring using automated emailed surveys (every 2 weeks). Personalized exercise prescriptions containing aerobic and resistance activities were implemented by cancer exercise specialists. Symptom-triggered synchronous sessions were initiated for participants failing to improve in CRF, as identified by a reference chart of CRF improvements observed during a supervised exercise program. Eligible participants were adult survivors of any cancer diagnosis who had completed treatment with curative intent in the past 12 months or had no planned changes in treatment for the duration of the study, lived in a rural area, and were currently experiencing CRF. Feasibility was assessed by objective measures of recruitment, data collection, intervention acceptability and suitability, and preliminary evaluations of participant responses. CRF was the primary clinical outcome (assessed using the Functional Assessment of Chronic Illness Therapy-Fatigue Scale [FACIT-Fatigue]) and was measured before, after, and 6 months after program completion.</p><p><strong>Results: </strong>In total, 19 participants enrolled in the study, 16 initiated the exercise program, and 15 completed the program. A total of 14 participants were recruited through internet advertisements, and the total recruitment rate peaked at 5 participants per month. Participants completed 100% of initial and final assessments (30 assessments across all participants) and 93% (70/75 possible surveys across all participants) of emailed surveys and attended 97% (29/30 possible sessions across all participants) of synchronous exercise sessions. In total, 6 participants initiated symptom-triggered sessions, with 6 of 7 initiated sessions attended. The mean FACIT-Fatigue scores significantly improved (P=.001) by 11.2 (SD 6.8) points following the completion of the program. A total of 13 participants demonstrated at least a minimal clinically important difference in FACIT-Fatigue scores (≥ +3 points) at this time. FACIT-Fatigue scores did not significantly change from program completion to 6-month follow-up (n=13; mea
背景:运动干预是治疗癌症相关性疲劳(CRF)最著名的干预措施之一。然而,农村地区的癌症幸存者报告说,参与锻炼计划存在特定障碍,并且缺乏全面的有效计划。目的:本研究的目的是评估一种专门为农村CRF癌症幸存者设计的新型远程医疗锻炼方案的可行性。方法:对BfitBwell远程医疗项目进行单臂临床试验。基于一个已建立的临床项目,这个经过调整的为期12周的项目通过提供同步视频会议锻炼课程(每个项目2次),使用个人训练智能手机或互联网应用程序的异步锻炼课程(每周3-5次),以及使用自动电子邮件调查(每两周)进行定期症状(CRF)监测,解决了以前农村幸存者报告的障碍。癌症运动专家实施了包含有氧和抵抗运动的个性化运动处方。在有监督的锻炼项目中观察到CRF改善的参考图表,对于CRF改善失败的参与者,启动症状触发的同步会话。符合条件的参与者是任何癌症诊断的成年幸存者,他们在过去12个月内完成了以治愈为目的的治疗,或者在研究期间没有计划改变治疗,居住在农村地区,目前正在经历CRF。通过招募、数据收集、干预的可接受性和适宜性以及参与者反应的初步评估来评估可行性。CRF是主要临床结果(使用慢性疾病治疗-疲劳量表的功能评估[facit -疲劳量表]进行评估),并在项目完成前、后和6个月进行测量。结果:总共有19名参与者参加了这项研究,16人开始了锻炼计划,15人完成了锻炼计划。通过网络广告共招募了14名参与者,总招募率最高为每月5名参与者。参与者完成了100%的初始和最终评估(所有参与者中30个评估)和93%(所有参与者中70/75个可能的调查)的电子邮件调查,并参加了97%(所有参与者中29/30个可能的会话)的同步锻炼课程。总共有6名参与者启动了症状触发型会议,7个启动的会议中有6个参加了会议。在项目完成后,FACIT-Fatigue平均得分显著提高了11.2 (SD 6.8)分(P= 0.001)。共有13名参与者在facit -疲劳评分(≥+3分)上表现出至少最小的临床重要差异。facit -疲劳评分从项目完成到6个月的随访没有显著变化(n=13;平均变化-1.1,标准差3.4点;P = 29)。结论:本研究结果支持BfitBwell远程医疗项目和后续疗效试验的可行性。新的项目组件也为通过异步运动处方和症状监测来提高运动项目的功效和效率提供了潜在的模型。试验注册:ClinicalTrials.gov NCT04533165;https://clinicaltrials.gov/study/NCT04533165。
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引用次数: 0
Exploring Motives Behind Ideal Melanoma Survivorship Care Plans With Multiple Stakeholders: A Cocreation Study. 探索背后的动机理想黑色素瘤生存护理计划与多方利益相关者:共同创造的研究。
IF 3.3 Q2 ONCOLOGY Pub Date : 2025-01-02 DOI: 10.2196/55746
Nadia Christina Willemina Kamminga, Marjolein Lugtenberg, Julia Annabel Van den Broek, Tamar Nijsten, Marlies Wakkee, Kasia Tabeau
<p><strong>Background: </strong>Survivorship care plans (SCPs), ie, personalized health care plans for cancer survivors, can be used to support the growing group of melanoma survivors throughout their disease trajectory. However, implementation and effectiveness of SCPs are suboptimal and could benefit from the involvement of stakeholders in developing a user-centered design.</p><p><strong>Objective: </strong>The aim of this study was to identify the ideal SCP for patients with melanoma in terms of functions and features to be included according to different stakeholders and to explore their underlying motives.</p><p><strong>Methods: </strong>In total, 3 cocreation sessions were organized with mixed samples of stakeholders, ie, patients with (a history of) melanoma (n=4), health care providers (HCPs) active in melanoma care (n=3), and IT specialists active in hospital IT departments (n=6). They were invited to compose their ideal melanoma SCP based on potential functions and features identified from prior qualitative research. These functions and features belonged to one of the four main categories of survivorship care (SSC): (1) information and education, (2) identification and treatment, (3) oncological follow-up, and (4) coordination. Participants were invited to explain their motives for including functions and features. Ideas were shared between stakeholders, and interaction was promoted. Descriptive statistics were used to determine the ideal SCP per stakeholder group. To analyze underlying motives, all cocreation sessions were audio-taped, transcribed verbatim, and analyzed in a thematic content analysis.</p><p><strong>Results: </strong>With regard to their ideal SCPs, all stakeholders added functions from all 4 SSC categories. Patients assembled a rather compact SCP with category 2 on identification and treatment being most important. Both HCPs and IT professionals constructed a somewhat larger SCP, with category 3 on oncological follow-up being the most important aspect and HCPs also focusing on category 4 on coordination. As for the motives behind their ideal SCP compositions, patients predominantly added functions based on their personal experiences or experiences from fellow patients, whereas both HCPS and IT professionals based their compositions primarily on their respective areas of expertise: HCPs related their additions to their roles as medical practitioners; for example, in providing a complete treatment plan and obtaining informed consent, while IT professionals' contributions were mainly influenced by feasibility and privacy concerns.</p><p><strong>Conclusions: </strong>This cocreation study provides insights into stakeholders' ideal melanoma SCP and the motivations behind them. Considering the diversity in both the preferences and underlying motives regarding SCP composition between patients, HCPs, and IT specialists, it is crucial to develop a broad SCP that extends beyond traditional SCP content, emphasizing personalizatio
背景:幸存者护理计划(SCPs),即针对癌症幸存者的个性化医疗保健计划,可用于支持越来越多的黑色素瘤幸存者的整个疾病轨迹。然而,scp的实施和有效性是次优的,可以从利益相关者参与开发以用户为中心的设计中获益。目的:本研究的目的是根据不同的利益相关者,确定黑色素瘤患者理想的SCP的功能和特征,并探讨其潜在的动机。方法:共组织了3次共同创造会议,参与者包括有黑色素瘤病史的患者(n=4)、从事黑色素瘤护理的医疗保健提供者(n=3)和医院IT部门的IT专家(n=6)。他们被邀请根据先前定性研究确定的潜在功能和特征组成理想的黑色素瘤SCP。这些功能和特征属于生存关怀(SSC)的四个主要类别之一:(1)信息和教育,(2)识别和治疗,(3)肿瘤随访,(4)协调。参与者被邀请解释他们加入功能和特性的动机。利益相关者之间分享了想法,促进了互动。描述性统计用于确定每个利益相关者群体的理想SCP。为了分析潜在的动机,所有的共同创造会议都被录音,逐字记录下来,并在主题内容分析中进行分析。结果:对于理想的scp,所有利益相关者都添加了所有4种SSC类别的功能。患者组装了一个相当紧凑的SCP,第2类的识别和治疗是最重要的。HCPs和IT专业人员都构建了一个更大的SCP,第3类肿瘤随访是最重要的方面,HCPs也关注第4类协调。至于他们理想的SCP组合物背后的动机,患者主要是根据他们的个人经验或其他患者的经验添加功能,而医护人员和IT专业人员主要是根据他们各自的专业领域添加功能:医护人员将他们添加的功能与他们作为医生的角色联系起来;例如,在提供完整的治疗计划和获得知情同意方面,而IT专业人员的贡献主要受到可行性和隐私问题的影响。结论:这项共同创造研究提供了利益相关者理想的黑色素瘤SCP及其背后动机的见解。考虑到患者、HCPs和IT专家在SCP组成方面的偏好和潜在动机的多样性,开发一种超越传统SCP内容、强调个性化的广泛SCP是至关重要的。除了利益相关者的持续参与外,还应努力解决潜在的可行性和隐私问题,以确保SCP满足患者和医护人员的需求。
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引用次数: 0
Implementation of Regular Lifestyle Counseling During Long-Term Follow-Up Care of Childhood Cancer Survivors: Monocentric Prospective Study. 儿童癌症幸存者长期随访护理中定期生活方式咨询的实施:单中心前瞻性研究。
IF 3.3 Q2 ONCOLOGY Pub Date : 2024-12-26 DOI: 10.2196/59614
Franziska Richter, Lea Louisa Kronziel, Inke König, Thorsten Langer, Judith Gebauer

Background: Many childhood cancer survivors (CCS) develop treatment-related late effects, including an increased risk of obesity and metabolic syndrome. A healthy lifestyle can reduce the risk of associated comorbidities. Therefore, at-risk CCS could benefit from lifestyle counseling during regular long-term follow-up (LTFU).

Objective: We implemented a new form of care to decrease the long-term morbidity among CCS and to gain new insights into the lifestyle of those patients.

Methods: Over a 1-year study period, lifestyle counseling was integrated into LTFU care. Metabolic disorders, including hypercholesterolemia, diabetes mellitus, overweight or underweight, and low activity levels, were assessed as screening parameters for various risk groups. The perspectives of CCS, physicians, and sports scientists were compared to identify those with the highest needs. Each lifestyle counseling included general recommendations for physical activity, as well as an assessment of individual preferences for and barriers to the implementation of a healthy lifestyle. A follow-up appointment after 1 month was performed.

Results: Of the 155 CCS aged 18 to 63 years (n=100, 65% female and n=55, 35% male), 112 (72%) had an indication for lifestyle counseling, identified by physicians, sports scientists, or the CCS themselves. Metabolic disorders affected 45% (n=70) of these CCS, and 46% (n=72) did not meet recommended activity levels. A total of 120 (77%) CCS received lifestyle counseling, including 8 initially uninterested individuals who became open to recommendations. Those with intensive cancer treatment history showed the greatest need. A total of 65 (54%) CCS were advised to change their lifestyle in both areas (diet and exercise) while 51 (43%) CCS received recommendations for only exercise (n=43 CCS, 36%) or diet (n=8 CCS, 7%). A total of 4 (3%) CCS, although interested in counseling, received no advice, as they already met the recommendations. Follow-up revealed high adherence to recommendations and successful integration into daily lives. In total, 97% (n=150) of survivors indicated that the provision of lifestyle counseling during LTFU would be generally beneficial.

Conclusions: Incorporating specialized health care professionals such as sports scientists into survivorship care enhances the multidisciplinary approach of LTFU care. Promoting a healthy lifestyle by offering guideline-based lifestyle counseling is broadly accepted among CCS and may reduce long-term morbidity.

背景:许多儿童癌症幸存者(CCS)出现治疗相关的后期效应,包括肥胖和代谢综合征的风险增加。健康的生活方式可以降低相关合并症的风险。因此,在定期长期随访(LTFU)期间,高危CCS患者可以从生活方式咨询中获益。目的:我们实施了一种新的护理形式,以降低CCS患者的长期发病率,并对这些患者的生活方式有了新的认识。方法:在1年的研究期间,生活方式咨询被纳入LTFU护理。代谢紊乱,包括高胆固醇血症、糖尿病、超重或体重不足、低活动水平,被评估为各种风险群体的筛选参数。比较了CCS、医生和运动科学家的观点,以确定那些需求最高的人。每项生活方式咨询都包括对身体活动的一般建议,以及对个人偏好和实施健康生活方式的障碍的评估。1个月后进行随访预约。结果:在155名年龄在18至63岁的CCS (n=100, 65%为女性,n=55, 35%为男性)中,112名(72%)有生活方式咨询的指征,由医生、运动科学家或CCS自己确定。代谢紊乱影响了45% (n=70)的CCS, 46% (n=72)没有达到推荐的活动水平。共有120名(77%)CCS接受了生活方式咨询,其中包括8名最初不感兴趣的人,后来接受了建议。那些有强烈癌症治疗史的患者表现出最大的需求。共有65名(54%)CCS被建议在两个方面(饮食和运动)改变他们的生活方式,而51名(43%)CCS只收到了运动(n=43名CCS, 36%)或饮食(n=8名CCS, 7%)的建议。总共有4个(3%)CCS,虽然对咨询感兴趣,但没有得到建议,因为他们已经达到了建议。随访显示,患者对建议的依从性很高,并成功融入日常生活。总共有97% (n=150)的幸存者表示,在LTFU期间提供生活方式咨询通常是有益的。结论:将专业卫生保健专业人员如运动科学家纳入生存护理,可提高LTFU护理的多学科方法。通过提供基于指南的生活方式咨询来促进健康的生活方式在CCS中被广泛接受,并可能降低长期发病率。
{"title":"Implementation of Regular Lifestyle Counseling During Long-Term Follow-Up Care of Childhood Cancer Survivors: Monocentric Prospective Study.","authors":"Franziska Richter, Lea Louisa Kronziel, Inke König, Thorsten Langer, Judith Gebauer","doi":"10.2196/59614","DOIUrl":"10.2196/59614","url":null,"abstract":"<p><strong>Background: </strong>Many childhood cancer survivors (CCS) develop treatment-related late effects, including an increased risk of obesity and metabolic syndrome. A healthy lifestyle can reduce the risk of associated comorbidities. Therefore, at-risk CCS could benefit from lifestyle counseling during regular long-term follow-up (LTFU).</p><p><strong>Objective: </strong>We implemented a new form of care to decrease the long-term morbidity among CCS and to gain new insights into the lifestyle of those patients.</p><p><strong>Methods: </strong>Over a 1-year study period, lifestyle counseling was integrated into LTFU care. Metabolic disorders, including hypercholesterolemia, diabetes mellitus, overweight or underweight, and low activity levels, were assessed as screening parameters for various risk groups. The perspectives of CCS, physicians, and sports scientists were compared to identify those with the highest needs. Each lifestyle counseling included general recommendations for physical activity, as well as an assessment of individual preferences for and barriers to the implementation of a healthy lifestyle. A follow-up appointment after 1 month was performed.</p><p><strong>Results: </strong>Of the 155 CCS aged 18 to 63 years (n=100, 65% female and n=55, 35% male), 112 (72%) had an indication for lifestyle counseling, identified by physicians, sports scientists, or the CCS themselves. Metabolic disorders affected 45% (n=70) of these CCS, and 46% (n=72) did not meet recommended activity levels. A total of 120 (77%) CCS received lifestyle counseling, including 8 initially uninterested individuals who became open to recommendations. Those with intensive cancer treatment history showed the greatest need. A total of 65 (54%) CCS were advised to change their lifestyle in both areas (diet and exercise) while 51 (43%) CCS received recommendations for only exercise (n=43 CCS, 36%) or diet (n=8 CCS, 7%). A total of 4 (3%) CCS, although interested in counseling, received no advice, as they already met the recommendations. Follow-up revealed high adherence to recommendations and successful integration into daily lives. In total, 97% (n=150) of survivors indicated that the provision of lifestyle counseling during LTFU would be generally beneficial.</p><p><strong>Conclusions: </strong>Incorporating specialized health care professionals such as sports scientists into survivorship care enhances the multidisciplinary approach of LTFU care. Promoting a healthy lifestyle by offering guideline-based lifestyle counseling is broadly accepted among CCS and may reduce long-term morbidity.</p>","PeriodicalId":45538,"journal":{"name":"JMIR Cancer","volume":"10 ","pages":"e59614"},"PeriodicalIF":3.3,"publicationDate":"2024-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11694152/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142899212","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluating Online Cannabis Health Information for Thai Breast Cancer Survivors Using the Quality Evaluation Scoring Tool (QUEST): Mixed Method Study. 使用质量评估评分工具(QUEST)评估泰国乳腺癌幸存者的在线大麻健康信息:混合方法研究
IF 3.3 Q2 ONCOLOGY Pub Date : 2024-12-24 DOI: 10.2196/55300
Thanarpan Peerawong, Tharin Phenwan, Meiko Makita, Sojirat Supanichwatana, Panupong Puttarak, Naowanit Siammai, Prakaidao Sunthorn
<p><strong>Background: </strong>Following medical cannabis legalization in Thailand in 2019, more people are seeking medical cannabis-related information, including women living with breast cancer. The extent to which they access cannabis-related information from internet sources and social media platforms and the quality of such content are relatively unknown and need further evaluation.</p><p><strong>Objective: </strong>This study aims to analyze the factors determining cannabis-related content quality for breast cancer care from internet sources and on social media platforms and examine the characteristics of such content accessed and consumed by Thai breast cancer survivors.</p><p><strong>Methods: </strong>A mixed methods study was conducted between January 2021 and May 2022, involving a breast cancer survivor support group. The group identified medical cannabis-related content from frequently accessed internet sources and social media platforms. The contents were categorized based on content creators, platforms, content category, and upload dates. Four researchers used the Quality Evaluation Scoring Tool (QUEST) to assess content quality, with scores ranging from 0 to 28. Contents were expert-rated as either high or poor. The QUEST interobserver reliability was analyzed. Receiver-operating characteristic curve analysis with the Youden index was used to determine the QUEST score cut-off point. Statistical significance was set at P<.05. Fairclough Critical Discourse Analysis was undertaken to examine the underlying discourses around poor-quality content.</p><p><strong>Results: </strong>Sixty-two Thai-language cannabis-related items were evaluated. The content sources were categorized as follows: news channels (21/62, 34%), government sources (16/62, 26%), health care providers (12/62, 19%), and alternative medicine providers (12/62, 19%). Most of the contents (30/62, 48%) were uploaded to YouTube, whereas 31% (19/62) appeared on websites and Facebook. Forty of 62 content items (64%) were news-related and generic cannabis advertisements while 8 of 62 (13%) content items had no identifiable date. The interobserver QUEST score correlation was 0.86 (P<.001). The mean QUEST score was 12.1 (SD 7.6). Contents were considered "high" when the expert rating was >3. With a QUEST score of 15 as the threshold, the sensitivity and specificity for differentiating between high and poor content quality were 81% and 98%, respectively. Content creation was the only significant factor between high- and poor-quality content. Poor-quality contents were primarily created by alternative medicine providers and news channels. Two discourses were identified: advocacy for cannabis use normalization and cannabis romanticization as a panacea. These discourses overly normalize and romanticize the use of cannabis, focusing on indications and instructions for cannabis use, and medical cannabis promotion, while neglecting discussions on cannabis contraindications and potential
背景:随着2019年泰国医用大麻合法化,越来越多的人寻求医用大麻相关信息,包括患有乳腺癌的女性。他们从互联网来源和社交媒体平台获取大麻相关信息的程度以及这些内容的质量相对未知,需要进一步评估。目的:本研究旨在分析影响互联网和社交媒体平台上乳腺癌护理大麻相关内容质量的因素,并研究泰国乳腺癌幸存者访问和消费此类内容的特征。方法:在2021年1月至2022年5月期间进行了一项混合方法研究,涉及乳腺癌幸存者支持小组。该组织从经常访问的互联网资源和社交媒体平台上确定了与医用大麻相关的内容。根据内容创建者、平台、内容类别和上传日期对内容进行分类。四名研究人员使用质量评估评分工具(QUEST)评估内容质量,得分范围从0到28。内容被专家评价为高或差。对QUEST观察者间信度进行了分析。采用约登指数进行患者工作特征曲线分析,确定QUEST评分的分界点。结果:评估了62个泰语大麻相关项目。内容来源分类如下:新闻频道(21/ 62,34%)、政府来源(16/ 62,26%)、卫生保健提供者(12/ 62,19%)和替代医学提供者(12/ 62,19%)。大部分内容(30/62,48%)上传到YouTube, 31%(19/62)出现在网站和Facebook上。62个内容项中有40个(64%)是与新闻相关的通用大麻广告,而62个内容项中有8个(13%)没有可识别的日期。观察者间QUEST评分相关性为0.86 (P3)。以QUEST评分15为阈值,区分内容质量好坏的敏感性和特异性分别为81%和98%。内容创作是区分高质量内容和低质量内容的唯一重要因素。低质量的内容主要是由替代医学提供者和新闻频道创造的。确定了两种话语:倡导大麻使用正常化和大麻浪漫化作为灵丹妙药。这些论述将大麻的使用过度正常化和浪漫化,侧重于大麻使用的适应症和说明以及医用大麻的推广,而忽视了对大麻禁忌症和潜在副作用的讨论。结论:泰国乳腺癌幸存者访问和分享的互联网资源和社交媒体平台上的医疗大麻相关信息质量参差不齐,这是一个令人担忧的问题。鉴于内容创作者是高内容质量的唯一预测因素,未来的研究应检查公众和患者可获得的更广泛的大麻相关来源,以更全面地了解这一问题。
{"title":"Evaluating Online Cannabis Health Information for Thai Breast Cancer Survivors Using the Quality Evaluation Scoring Tool (QUEST): Mixed Method Study.","authors":"Thanarpan Peerawong, Tharin Phenwan, Meiko Makita, Sojirat Supanichwatana, Panupong Puttarak, Naowanit Siammai, Prakaidao Sunthorn","doi":"10.2196/55300","DOIUrl":"10.2196/55300","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Following medical cannabis legalization in Thailand in 2019, more people are seeking medical cannabis-related information, including women living with breast cancer. The extent to which they access cannabis-related information from internet sources and social media platforms and the quality of such content are relatively unknown and need further evaluation.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;This study aims to analyze the factors determining cannabis-related content quality for breast cancer care from internet sources and on social media platforms and examine the characteristics of such content accessed and consumed by Thai breast cancer survivors.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;A mixed methods study was conducted between January 2021 and May 2022, involving a breast cancer survivor support group. The group identified medical cannabis-related content from frequently accessed internet sources and social media platforms. The contents were categorized based on content creators, platforms, content category, and upload dates. Four researchers used the Quality Evaluation Scoring Tool (QUEST) to assess content quality, with scores ranging from 0 to 28. Contents were expert-rated as either high or poor. The QUEST interobserver reliability was analyzed. Receiver-operating characteristic curve analysis with the Youden index was used to determine the QUEST score cut-off point. Statistical significance was set at P&lt;.05. Fairclough Critical Discourse Analysis was undertaken to examine the underlying discourses around poor-quality content.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Sixty-two Thai-language cannabis-related items were evaluated. The content sources were categorized as follows: news channels (21/62, 34%), government sources (16/62, 26%), health care providers (12/62, 19%), and alternative medicine providers (12/62, 19%). Most of the contents (30/62, 48%) were uploaded to YouTube, whereas 31% (19/62) appeared on websites and Facebook. Forty of 62 content items (64%) were news-related and generic cannabis advertisements while 8 of 62 (13%) content items had no identifiable date. The interobserver QUEST score correlation was 0.86 (P&lt;.001). The mean QUEST score was 12.1 (SD 7.6). Contents were considered \"high\" when the expert rating was &gt;3. With a QUEST score of 15 as the threshold, the sensitivity and specificity for differentiating between high and poor content quality were 81% and 98%, respectively. Content creation was the only significant factor between high- and poor-quality content. Poor-quality contents were primarily created by alternative medicine providers and news channels. Two discourses were identified: advocacy for cannabis use normalization and cannabis romanticization as a panacea. These discourses overly normalize and romanticize the use of cannabis, focusing on indications and instructions for cannabis use, and medical cannabis promotion, while neglecting discussions on cannabis contraindications and potential","PeriodicalId":45538,"journal":{"name":"JMIR Cancer","volume":"10 ","pages":"e55300"},"PeriodicalIF":3.3,"publicationDate":"2024-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11693783/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142899174","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Designing Positive Psychology Interventions for Social Media: Cross-Sectional Web-Based Experiment With Young Adults With Cancer. 为社交媒体设计积极心理学干预措施:以患癌症的年轻成年人为对象的跨部门网络实验。
IF 3.3 Q2 ONCOLOGY Pub Date : 2024-12-20 DOI: 10.2196/48627
Allison J Lazard, Rhyan N Vereen, Jieni Zhou, Hazel B Nichols, Marlyn Pulido, Catherine Swift, Nabarun Dasgupta, Barbara L Fredrickson
<p><strong>Background: </strong>Young adults (ages 18-39 years) with cancer face unique risks for negative psychosocial outcomes. These risks could be lessened with positive psychology interventions adapted for social media if intervention messages encourage intentions to do the activities and positive message reactions and if young adults with cancer perceive few downsides.</p><p><strong>Objective: </strong>This study aimed to assess whether social media messages from evidence-based positive psychology interventions encouraged intentions to do the intervention activities and intended positive message reactions, overall and among sociodemographic or cancer characteristic subgroups. We also aimed to identify perceived downsides of the activity that would negatively impact the interventions' feasibility.</p><p><strong>Methods: </strong>Young adults (ages 18-39 years, cancer diagnosis ages 15-39 years) were randomized to a between-persons web-based experiment. Participants viewed a social media message with social context cues (vs not) for 1 of 2 types of intervention (acts of kindness vs social connectedness). Participants reported intentions to do the activity, along with their perceived social presence in the message (how much they felt the sense of others) and forecasted positivity resonance (whether they would experience socially connected positive emotions when doing the activity), with 5-point items. Participants also reported their self-efficacy (how certain they can do the intervention activity) with a 0-100 item and potential downsides of the activity categorically.</p><p><strong>Results: </strong>More than 4 out of 5 young adults with cancer (N=396) reported they "somewhat" (coded as 3) to "extremely" (5) intended to do the intervention activity (336/396, 84.8%; mean ranged from 3.4-3.6, SD 0.9-1.0), perceived social presence in the messages (350/396, 88.4%; mean 3.8, SD 0.7), and forecasted positivity resonance (349/396, 88.1%; mean 3.8-3.9, SD 0.8). Participants reported having self-efficacy to complete the activity (mean 70.7% of possible 100%, SD 15.4%-17.2%). Most (320/396, 80.8%) did not think of the downsides of the interventions. Messages with social context cues (vs not) and both intervention types were rated similarly (all P>.05). Black young adults reported lower intentions, perceived social presence, and forecasted positivity resonance than White young adults (all P<.001). Participants in active treatment (vs completed) reported greater intentions to do the activities (P<.001).</p><p><strong>Conclusions: </strong>Positive psychology intervention messages adapted for social media were perceived as acceptable and feasible among young adults with cancer. The social media-based messages encouraged increasing one's social connectedness and performing acts of kindness. Young adults with cancer also predicted they would have feelings of positive social engagement (positivity resonance) when doing the interventions-the key ingredient
背景:患有癌症的年轻人(18-39岁)面临着独特的负面心理社会结局风险。如果干预信息鼓励进行活动的意图和积极的信息反应,并且患有癌症的年轻成年人几乎没有感觉到负面影响,那么针对社交媒体的积极心理学干预可以降低这些风险。目的:本研究旨在评估基于证据的积极心理学干预的社交媒体信息是否在总体上以及在社会人口学或癌症特征亚组中鼓励了进行干预活动的意愿和预期的积极信息反应。我们还旨在确定可能对干预措施的可行性产生负面影响的活动的负面影响。方法:年轻人(年龄在18-39岁,癌症诊断年龄在15-39岁)被随机分配到一个基于网络的人际实验中。参与者在两种干预(善意行为与社会联系)中的一种中观看了带有社会背景线索的社交媒体信息(与不带有社会背景线索的对照)。参与者报告了做这项活动的意图,以及他们在信息中感知到的社会存在感(他们感受到他人的感觉有多强烈)和预测的积极共鸣(他们在做这项活动时是否会体验到与社会相关的积极情绪)。参与者还用0-100分的项目分类地报告了他们的自我效能感(他们对干预活动的肯定程度)和活动的潜在缺点。结果:超过4 / 5的年轻癌症患者(N=396)报告他们“有点”(编码为3)到“非常”(编码为5)打算进行干预活动(336/396,84.8%;平均值为3.4-3.6,标准差为0.9-1.0),信息中感知到的社会存在(350/396,88.4%;平均3.8,标准差0.7),预测阳性共振(349/396,88.1%;平均值3.8-3.9,标准差0.8)。参与者报告在完成活动时具有自我效能感(平均为70.7%,标准差为15.4%-17.2%)。大多数(320/396,80.8%)没有想到干预措施的负面影响。具有社会背景线索的信息(与不具有)和两种干预类型的评价相似(P均为0.05)。与白人青年相比,黑人青年报告的意向、感知的社会存在和预测的积极共振较低(所有结论:适应社交媒体的积极心理干预信息在患有癌症的青年中被认为是可接受和可行的。基于社交媒体的信息鼓励增加一个人的社会联系和做善事。患有癌症的年轻人还预测,在进行干预时,他们会有积极的社会参与感(积极的共鸣),这是体验这些活动对健康有益的关键因素。这项研究为开发适合年龄的、高度可扩展的干预措施来改善年轻癌症患者的心理社会健康提供了有希望的证据。
{"title":"Designing Positive Psychology Interventions for Social Media: Cross-Sectional Web-Based Experiment With Young Adults With Cancer.","authors":"Allison J Lazard, Rhyan N Vereen, Jieni Zhou, Hazel B Nichols, Marlyn Pulido, Catherine Swift, Nabarun Dasgupta, Barbara L Fredrickson","doi":"10.2196/48627","DOIUrl":"10.2196/48627","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Young adults (ages 18-39 years) with cancer face unique risks for negative psychosocial outcomes. These risks could be lessened with positive psychology interventions adapted for social media if intervention messages encourage intentions to do the activities and positive message reactions and if young adults with cancer perceive few downsides.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;This study aimed to assess whether social media messages from evidence-based positive psychology interventions encouraged intentions to do the intervention activities and intended positive message reactions, overall and among sociodemographic or cancer characteristic subgroups. We also aimed to identify perceived downsides of the activity that would negatively impact the interventions' feasibility.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;Young adults (ages 18-39 years, cancer diagnosis ages 15-39 years) were randomized to a between-persons web-based experiment. Participants viewed a social media message with social context cues (vs not) for 1 of 2 types of intervention (acts of kindness vs social connectedness). Participants reported intentions to do the activity, along with their perceived social presence in the message (how much they felt the sense of others) and forecasted positivity resonance (whether they would experience socially connected positive emotions when doing the activity), with 5-point items. Participants also reported their self-efficacy (how certain they can do the intervention activity) with a 0-100 item and potential downsides of the activity categorically.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;More than 4 out of 5 young adults with cancer (N=396) reported they \"somewhat\" (coded as 3) to \"extremely\" (5) intended to do the intervention activity (336/396, 84.8%; mean ranged from 3.4-3.6, SD 0.9-1.0), perceived social presence in the messages (350/396, 88.4%; mean 3.8, SD 0.7), and forecasted positivity resonance (349/396, 88.1%; mean 3.8-3.9, SD 0.8). Participants reported having self-efficacy to complete the activity (mean 70.7% of possible 100%, SD 15.4%-17.2%). Most (320/396, 80.8%) did not think of the downsides of the interventions. Messages with social context cues (vs not) and both intervention types were rated similarly (all P&gt;.05). Black young adults reported lower intentions, perceived social presence, and forecasted positivity resonance than White young adults (all P&lt;.001). Participants in active treatment (vs completed) reported greater intentions to do the activities (P&lt;.001).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;Positive psychology intervention messages adapted for social media were perceived as acceptable and feasible among young adults with cancer. The social media-based messages encouraged increasing one's social connectedness and performing acts of kindness. Young adults with cancer also predicted they would have feelings of positive social engagement (positivity resonance) when doing the interventions-the key ingredient ","PeriodicalId":45538,"journal":{"name":"JMIR Cancer","volume":"10 ","pages":"e48627"},"PeriodicalIF":3.3,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11675907/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142869716","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Prototype of an App Designed to Support Self-Management for Health Behaviors and Weight in Women Living With Breast Cancer: Qualitative User Experience Study. 旨在支持乳腺癌女性患者自我管理健康行为和体重的应用程序原型:定性用户体验研究。
IF 3.3 Q2 ONCOLOGY Pub Date : 2024-12-20 DOI: 10.2196/48170
Phillippa Lally, Christine N May, E Siobhan Mitchell, Meaghan McCallum, Andreas Michaelides, Abigail Fisher

Background: Accessible self-management interventions are required to support people living with breast cancer.

Objective: This was an industry-academic partnership study that aimed to collect qualitative user experience data of a prototype app with built-in peer and coach support designed to support the management of health behaviors and weight in women living with breast cancer.

Methods: Participants were aged ≥18 years, were diagnosed with breast cancer of any stage within the last 5 years, had completed active treatment, and were prescribed oral hormone therapy. Participants completed demographic surveys and were asked to use the app for 4 weeks. Following this, they took part in in-depth qualitative interviews about their experiences. These were analyzed using thematic analysis.

Results: Eight participants (mean age, 45 years; mean time since diagnosis, 32 months) were included. Of the 8 participants, 7 (88%) were white, 6 (75%) had a graduate degree or above, and 6 (75%) had stage I-III breast cancer. Four overarching themes were identified: (1) Support for providing an app earlier in the care pathway; (2) Desire for more weight-focused content tailored to the breast cancer experience; (3) Tracking of health behaviors that are generally popular; and (4) High value of in-app social support.

Conclusions: This early user experience work showed that women with breast cancer found an app with integrated social and psychological support appealing to receive support for behavior change and weight management or self-management. However, many features were recommended for further development. This work is the first step in an academic-industry collaboration that would ultimately aim to develop and empirically test a supportive app that could be integrated into the cancer care pathway.

背景:需要可获得的自我管理干预措施来支持乳腺癌患者。目的:这是一项行业-学术合作研究,旨在收集具有内置同伴和教练支持的原型应用程序的定性用户体验数据,旨在支持乳腺癌女性患者的健康行为和体重管理。方法:参与者年龄≥18岁,在过去5年内被诊断为乳腺癌的任何阶段,已完成积极治疗,并给予口服激素治疗。参与者完成了人口统计调查,并被要求使用该应用程序4周。在此之后,他们参加了关于他们经历的深度定性访谈。使用主题分析对这些进行了分析。结果:8名参与者(平均年龄45岁;平均诊断时间为32个月)。在8名参与者中,7名(88%)是白人,6名(75%)拥有研究生或以上学位,6名(75%)患有I-III期乳腺癌。确定了四个总体主题:(1)支持在护理途径的早期提供应用程序;(2)希望获得更多针对乳腺癌体验的以体重为重点的内容;(3)跟踪普遍流行的健康行为;(4)应用内社交支持价值高。结论:这项早期的用户体验研究表明,患有乳腺癌的女性发现,一款具有综合社会和心理支持的应用程序很有吸引力,可以获得行为改变、体重管理或自我管理方面的支持。然而,许多特性被推荐用于进一步开发。这项工作是学术与行业合作的第一步,最终目标是开发和实证测试一款可以整合到癌症治疗途径中的支持性应用程序。
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JMIR Cancer
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