首页 > 最新文献

JMIR Rehabilitation and Assistive Technologies最新文献

英文 中文
Validation of Gait Kinematics With Ramp and Stair Ascent and Descent Revealed by Markerless Motion Capture in Simulated Living Space: Test-Retest Reliability Study. 基于无标记动作捕捉的模拟生活空间坡道和楼梯升降步态运动学验证:重测可靠性研究。
Q2 Medicine Pub Date : 2025-05-15 DOI: 10.2196/66886
Daiki Shimotori, Kenji Kato, Tatsuya Yoshimi, Izumi Kondo

Background: In recent years, there has been an increasing demand for markerless motion capture systems, which are being widely used in biomechanical and clinical research. Furthermore, by using a markerless motion capture system in a laboratory environment that mimics living spaces, the data acquired on various activities of daily living, such as level walking, ramp walking, and stair ascent and descent, should more closely resemble that of real-life activities. However, the absolute reliability of gait parameters in this context is still unclear.

Objective: The aim of this study was to evaluate the reliability of a markerless motion capture system in assessing the ascent and descent of ramps and stairs during walking in a simulated living space.

Methods: A total of 21 healthy participants performed level walking, ramp and stair ascent and descent on two separate days, with at least a 24-hour interval between sessions. Joint angles were measured using 27 synchronized cameras with a markerless motion capture application, Theia3D (Theia Markerless Inc), and analyzed in Visual3d for all planes of motion at the hip-, knee-, and ankle-joints. The absolute reliability of day-to-day reproducibility was assessed using full-curve analysis (root mean square difference [RMSD]) and discrete point analysis of gait events using the standard error of measurement (SEM). SEM was calculated only for level walking and ramp ascent and descent, where gait events were correctly detected.

Results: The SEM values for level walking and ramp ascent and descent were all below the 5-degree threshold. However, while RMSD values were generally below 5°, this threshold was exceeded for knee-joint flexion-extension angles during ramp ascent and stair ascent (5.07° and 5.64°, respectively).

Conclusions: The markerless motion capture system in the living laboratory setting demonstrated a high degree of accuracy for various environments and gait types. The low SEM values obtained indicate good reliability for joint angle measurements across different days. The slightly higher RMSD values for knee-joint angles during ramp and stair ascent may reflect the system's ability to capture the adaptations in joint kinematics in response to changes in gait conditions. These measurements in a living laboratory environment validated the absolute reliability of various gait parameters not only in level walking but also in ramp and stair ascent and descent. The findings suggest potential clinical applications and research opportunities, including the development of assistive devices and robots, using markerless motion capture in more natural living situations, rather than in controlled environments.

背景:近年来,人们对无标记运动捕捉系统的需求越来越大,在生物力学和临床研究中得到了广泛的应用。此外,通过在模拟生活空间的实验室环境中使用无标记动作捕捉系统,获得的日常生活中各种活动的数据,如水平行走、坡道行走和楼梯上下,应该更接近于现实生活中的活动。然而,在这种情况下,步态参数的绝对可靠性仍然不清楚。目的:本研究的目的是评估无标记运动捕捉系统在模拟生活空间中评估行走时斜坡和楼梯的上升和下降的可靠性。方法:共有21名健康参与者分别在两天内进行水平步行、坡道和楼梯上下运动,每次运动之间至少间隔24小时。关节角度使用27台同步摄像机与无标记运动捕捉应用程序Theia3D (Theia markerless Inc)进行测量,并在Visual3d中分析髋关节、膝关节和踝关节的所有运动平面。使用全曲线分析(均方根差[RMSD])和使用测量标准误差(SEM)的步态事件离散点分析来评估日常重复性的绝对可靠性。扫描电镜只计算水平行走和斜坡上升和下降,其中步态事件被正确检测。结果:水平行走和坡道上下行走的扫描电镜值均低于5度阈值。然而,虽然RMSD值一般低于5°,但在斜坡上升和楼梯上升过程中膝关节屈伸角超过了这个阈值(分别为5.07°和5.64°)。结论:在生活实验室环境中,无标记运动捕捉系统显示出对各种环境和步态类型的高度准确性。所获得的低SEM值表明,在不同的日子接缝角度测量具有良好的可靠性。在坡道和楼梯上,膝关节角度的RMSD值略高,这可能反映了系统捕捉关节运动学适应步态变化的能力。这些在生活实验室环境中的测量验证了各种步态参数的绝对可靠性,不仅在水平行走中,而且在坡道和楼梯上升和下降中。这些发现表明了潜在的临床应用和研究机会,包括辅助设备和机器人的开发,在更自然的生活环境中使用无标记动作捕捉,而不是在受控环境中。
{"title":"Validation of Gait Kinematics With Ramp and Stair Ascent and Descent Revealed by Markerless Motion Capture in Simulated Living Space: Test-Retest Reliability Study.","authors":"Daiki Shimotori, Kenji Kato, Tatsuya Yoshimi, Izumi Kondo","doi":"10.2196/66886","DOIUrl":"10.2196/66886","url":null,"abstract":"<p><strong>Background: </strong>In recent years, there has been an increasing demand for markerless motion capture systems, which are being widely used in biomechanical and clinical research. Furthermore, by using a markerless motion capture system in a laboratory environment that mimics living spaces, the data acquired on various activities of daily living, such as level walking, ramp walking, and stair ascent and descent, should more closely resemble that of real-life activities. However, the absolute reliability of gait parameters in this context is still unclear.</p><p><strong>Objective: </strong>The aim of this study was to evaluate the reliability of a markerless motion capture system in assessing the ascent and descent of ramps and stairs during walking in a simulated living space.</p><p><strong>Methods: </strong>A total of 21 healthy participants performed level walking, ramp and stair ascent and descent on two separate days, with at least a 24-hour interval between sessions. Joint angles were measured using 27 synchronized cameras with a markerless motion capture application, Theia3D (Theia Markerless Inc), and analyzed in Visual3d for all planes of motion at the hip-, knee-, and ankle-joints. The absolute reliability of day-to-day reproducibility was assessed using full-curve analysis (root mean square difference [RMSD]) and discrete point analysis of gait events using the standard error of measurement (SEM). SEM was calculated only for level walking and ramp ascent and descent, where gait events were correctly detected.</p><p><strong>Results: </strong>The SEM values for level walking and ramp ascent and descent were all below the 5-degree threshold. However, while RMSD values were generally below 5°, this threshold was exceeded for knee-joint flexion-extension angles during ramp ascent and stair ascent (5.07° and 5.64°, respectively).</p><p><strong>Conclusions: </strong>The markerless motion capture system in the living laboratory setting demonstrated a high degree of accuracy for various environments and gait types. The low SEM values obtained indicate good reliability for joint angle measurements across different days. The slightly higher RMSD values for knee-joint angles during ramp and stair ascent may reflect the system's ability to capture the adaptations in joint kinematics in response to changes in gait conditions. These measurements in a living laboratory environment validated the absolute reliability of various gait parameters not only in level walking but also in ramp and stair ascent and descent. The findings suggest potential clinical applications and research opportunities, including the development of assistive devices and robots, using markerless motion capture in more natural living situations, rather than in controlled environments.</p>","PeriodicalId":36224,"journal":{"name":"JMIR Rehabilitation and Assistive Technologies","volume":"12 ","pages":"e66886"},"PeriodicalIF":0.0,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12097655/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144081168","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
Patients' Expectations for App-Based Therapy in Knee Osteoarthritis: User-Centered Design Approach. 膝关节骨性关节炎患者对应用程序治疗的期望:以用户为中心的设计方法
Q2 Medicine Pub Date : 2025-05-15 DOI: 10.2196/64607
Pika Krištof Mirt, Karmen Erjavec, Sabina Krsnik, Petra Kotnik, Hussein Mohsen

Background: Knee osteoarthritis (KOA) requires long-term treatment that faces significant barriers, including inadequate physiotherapy services, especially in Slovenia and comparable European countries. Mobile health apps offer a promising solution to improve accessibility and adherence to KOA treatment.

Objectives: This study aimed to identify expectations of patients with KOA for app-based therapy, determine the functional requirements, and assess the main barriers and benefits of using mobile apps for KOA management. It also examined these factors about demographic data (gender, age, and education level) and motivation to perform knee exercises.

Methods: A mixed methods approach was used, integrating quantitative data from a structured questionnaire and qualitative data from in-depth interviews. The purposive sample comprised 82 patients with symptomatic KOA graded 1-3 on the Kellgren-Lawrence scale, excluding those with cognitive impairments, wheelchair dependency, significant comorbidities, or language barriers.

Results: The analysis revealed that 53.7% (44/82) of patients preferred smartphones, while 40.2% (33/82) favored PCs for remote KOA management, citing accessibility and convenience. Exercise videos received the highest rating (µ=9.45), followed by goal setting and tracking (µ=8.95) and regular e-messages (µ=8.83). Telephone consultations with physiotherapists were also highly valued (µ=8.41). Significant differences were observed in the perceived importance of key disease information (F9=2.077; P=.04) and exercise videos (F9=2.788; P=.05) based on motivation levels but not by gender, age, or education. Perceptions of the appropriate duration of physical activity varied with motivation levels (F9=2.490; P=.02) but not with demographic factors. Men rated ease of use (4.93 vs 4.71; F1=3.961; P=.05) and the clarity of the exercise flow display higher than women. The most significant barrier was inaccurate disease information (µ=3.96), with notable differences across age groups. Younger participants (younger than 40 years) and those aged 51-60 years expressed concerns about time management and information accuracy. Patients highlighted the ability to rewatch exercises as a key app feature, while time efficiency and improved access to physiotherapists were highly valued for convenience. Enhanced communication and accurate information were essential for building trust and ensuring effective treatment.

Conclusions: Mobile health apps for KOA management should be designed with a user-centered approach, prioritizing accessibility, motivation, and effective communication. Key functionalities include high-quality exercise videos, goal setting, symptom tracking, and regular electronic reminders. Mitigating user-reported barriers and integrating age-specific adaptations can enhance adherence and therapeutic outcomes. The findings highlig

背景:膝关节骨性关节炎(KOA)需要长期治疗,但面临重大障碍,包括物理治疗服务不足,特别是在斯洛文尼亚和类似的欧洲国家。移动健康应用程序为提高KOA治疗的可及性和依从性提供了一个有希望的解决方案。目的:本研究旨在确定KOA患者对应用程序治疗的期望,确定功能需求,并评估使用移动应用程序进行KOA管理的主要障碍和益处。它还检查了人口统计数据(性别、年龄、教育水平)和进行膝关节运动的动机等因素。方法:采用混合方法,将结构化问卷的定量数据与深度访谈的定性数据相结合。目的样本包括82例症状性KOA患者,Kellgren-Lawrence评分为1-3级,排除认知障碍、轮椅依赖、显著合并症或语言障碍。结果:53.7%(44/82)的患者选择智能手机进行远程KOA管理,40.2%(33/82)的患者选择pc进行远程KOA管理,理由是方便快捷。运动视频的评分最高(µ=9.45),其次是目标设定和跟踪(µ=8.95)和定期电子邮件(µ=8.83)。与物理治疗师的电话咨询也很有价值(µ=8.41)。关键疾病信息感知重要性差异有统计学意义(F9=2.077;P=.04)和运动视频(F9=2.788;P= 0.05),但与性别、年龄或教育程度无关。对体育活动适当持续时间的看法随动机水平而变化(F9=2.490;P=.02),但与人口统计学因素无关。男性认为易用性(4.93 vs 4.71;F1 = 3.961;P= 0.05),运动流清晰度高于女性。最显著的障碍是疾病信息不准确(µ=3.96),不同年龄组之间存在显著差异。年轻的参与者(40岁以下)和51-60岁的参与者表达了对时间管理和信息准确性的担忧。患者强调,重新观看锻炼的能力是应用程序的一个关键功能,而时间效率和更好地获得物理治疗师的便利也受到了高度重视。加强沟通和提供准确信息对于建立信任和确保有效治疗至关重要。结论:用于KOA管理的移动健康应用程序应以用户为中心,优先考虑可访问性、动机和有效沟通。主要功能包括高质量的运动视频、目标设定、症状跟踪和定期电子提醒。减轻用户报告的障碍并结合年龄特异性适应可以增强依从性和治疗结果。研究结果强调了移动卫生技术在优化KOA自我管理和改善患者生活质量方面的潜力,特别是在斯洛文尼亚等物理治疗可及性有限的卫生保健系统中。
{"title":"Patients' Expectations for App-Based Therapy in Knee Osteoarthritis: User-Centered Design Approach.","authors":"Pika Krištof Mirt, Karmen Erjavec, Sabina Krsnik, Petra Kotnik, Hussein Mohsen","doi":"10.2196/64607","DOIUrl":"10.2196/64607","url":null,"abstract":"<p><strong>Background: </strong>Knee osteoarthritis (KOA) requires long-term treatment that faces significant barriers, including inadequate physiotherapy services, especially in Slovenia and comparable European countries. Mobile health apps offer a promising solution to improve accessibility and adherence to KOA treatment.</p><p><strong>Objectives: </strong>This study aimed to identify expectations of patients with KOA for app-based therapy, determine the functional requirements, and assess the main barriers and benefits of using mobile apps for KOA management. It also examined these factors about demographic data (gender, age, and education level) and motivation to perform knee exercises.</p><p><strong>Methods: </strong>A mixed methods approach was used, integrating quantitative data from a structured questionnaire and qualitative data from in-depth interviews. The purposive sample comprised 82 patients with symptomatic KOA graded 1-3 on the Kellgren-Lawrence scale, excluding those with cognitive impairments, wheelchair dependency, significant comorbidities, or language barriers.</p><p><strong>Results: </strong>The analysis revealed that 53.7% (44/82) of patients preferred smartphones, while 40.2% (33/82) favored PCs for remote KOA management, citing accessibility and convenience. Exercise videos received the highest rating (µ=9.45), followed by goal setting and tracking (µ=8.95) and regular e-messages (µ=8.83). Telephone consultations with physiotherapists were also highly valued (µ=8.41). Significant differences were observed in the perceived importance of key disease information (F9=2.077; P=.04) and exercise videos (F9=2.788; P=.05) based on motivation levels but not by gender, age, or education. Perceptions of the appropriate duration of physical activity varied with motivation levels (F9=2.490; P=.02) but not with demographic factors. Men rated ease of use (4.93 vs 4.71; F1=3.961; P=.05) and the clarity of the exercise flow display higher than women. The most significant barrier was inaccurate disease information (µ=3.96), with notable differences across age groups. Younger participants (younger than 40 years) and those aged 51-60 years expressed concerns about time management and information accuracy. Patients highlighted the ability to rewatch exercises as a key app feature, while time efficiency and improved access to physiotherapists were highly valued for convenience. Enhanced communication and accurate information were essential for building trust and ensuring effective treatment.</p><p><strong>Conclusions: </strong>Mobile health apps for KOA management should be designed with a user-centered approach, prioritizing accessibility, motivation, and effective communication. Key functionalities include high-quality exercise videos, goal setting, symptom tracking, and regular electronic reminders. Mitigating user-reported barriers and integrating age-specific adaptations can enhance adherence and therapeutic outcomes. The findings highlig","PeriodicalId":36224,"journal":{"name":"JMIR Rehabilitation and Assistive Technologies","volume":"12 ","pages":"e64607"},"PeriodicalIF":0.0,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12097652/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144081070","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
Co-Designed Digital Device for Tracking Rehabilitation Dosage in a Clinical Environment After Stroke: Mixed Methods Validity and Feasibility Study. 联合设计用于脑卒中后临床环境康复剂量跟踪的数字装置:混合方法的有效性和可行性研究。
Q2 Medicine Pub Date : 2025-05-14 DOI: 10.2196/68129
Fiona Boyd, Gillian Sweeney, Mark Barber, Elaine Forrest, Mark Dunlop, Andrew Kerr

Background: In 2023, the National Clinical Guidelines for Stroke revised the recommended daily multidisciplinary therapy dose from 45 minutes per therapy to 3 hours of therapy overall. To monitor the achievement of these guidelines, there is a need for accurate measurement. This study introduces a novel co-designed digital dosage tracking system that uses Near Field Communication technology to log rehabilitation activities and demonstrates its feasibility and accuracy in a clinical setting through comparison with the current clinical method of manual recording.

Objective: This study aimed to assess the validity, feasibility, and usability of a novel co-designed digital tracker using Near Field Communication technology to automatically log rehabilitation dosage in people with stroke history, providing an objective and low-burden solution for clinical environments.

Methods: This pilot mixed methods study included 2 phases. Phase 1 involved a usability trial with 9 participants conducted at a university research center, assessing usability with the System Usability Scale (SUS) and Intrinsic Motivation Inventory (IMI). Phase 2 consisted of a clinical trial in a National Health Service stroke ward with 15 inpatients, comparing the digital tracker with manual therapist recordings for validity and feasibility using paired t tests, Cohen d, and Bland-Altman plots. An acceptable discrepancy range was set at ±5%-10%.

Results: The digital tracker demonstrated high usability with a mean SUS score of 91.43 (SD 9.53) and strong user satisfaction (IMI score 6.29/7, SD 1.50). Clinical trial results showed a strong agreement between the digital and manual methods (t206=-1.60; P=.11; Cohen d=-0.06), with a small mean time discrepancy of 1.23 (SD 11.01) minutes across 207 activities. The Bland-Altman plot indicated good accuracy and consistency between methods, with limits of agreement within the clinically acceptable range.

Conclusions: The co-designed digital tracker has been shown to agree with a manual method for recording rehabilitation dosage. This development presents the opportunity for objective, automated, and low-burden recording of rehabilitation dose to support prescription, monitoring, and research.

背景:2023年,国家卒中临床指南将推荐的每日多学科治疗剂量从每次治疗45分钟修改为总治疗3小时。为了监测这些指导方针的实现情况,需要进行精确的测量。本研究介绍了一种新型的合作设计的数字剂量跟踪系统,该系统使用近场通信技术记录康复活动,并通过与目前临床手工记录方法的比较,证明了其在临床环境中的可行性和准确性。目的:本研究旨在评估一种新型协同设计的数字跟踪器的有效性、可行性和可用性,该跟踪器使用近场通信技术自动记录卒中患者的康复剂量,为临床环境提供客观、低负担的解决方案。方法:本试验分为两个阶段。阶段1包括在一个大学研究中心进行的有9名参与者的可用性试验,用系统可用性量表(SUS)和内在动机量表(IMI)评估可用性。第二阶段包括在国家卫生服务中风病房进行的临床试验,共有15名住院患者,使用配对t检验、Cohen d和Bland-Altman图比较数字跟踪器与手工治疗师记录的有效性和可行性。可接受的误差范围设定为±5%-10%。结果:该数字追踪器可用性高,平均SUS评分为91.43 (SD 9.53),用户满意度高(IMI评分为6.29/7,SD 1.50)。临床试验结果显示,数字方法与手工方法非常吻合(t206=-1.60;P =厚;Cohen d=-0.06),在207项活动中,平均时间差异很小,为1.23分钟(SD 11.01)。Bland-Altman图显示方法之间具有良好的准确性和一致性,在临床可接受的范围内具有一定的一致性。结论:共同设计的数字跟踪器已被证明与手动记录康复剂量的方法一致。这一发展为客观、自动化和低负担的康复剂量记录提供了机会,以支持处方、监测和研究。
{"title":"Co-Designed Digital Device for Tracking Rehabilitation Dosage in a Clinical Environment After Stroke: Mixed Methods Validity and Feasibility Study.","authors":"Fiona Boyd, Gillian Sweeney, Mark Barber, Elaine Forrest, Mark Dunlop, Andrew Kerr","doi":"10.2196/68129","DOIUrl":"10.2196/68129","url":null,"abstract":"<p><strong>Background: </strong>In 2023, the National Clinical Guidelines for Stroke revised the recommended daily multidisciplinary therapy dose from 45 minutes per therapy to 3 hours of therapy overall. To monitor the achievement of these guidelines, there is a need for accurate measurement. This study introduces a novel co-designed digital dosage tracking system that uses Near Field Communication technology to log rehabilitation activities and demonstrates its feasibility and accuracy in a clinical setting through comparison with the current clinical method of manual recording.</p><p><strong>Objective: </strong>This study aimed to assess the validity, feasibility, and usability of a novel co-designed digital tracker using Near Field Communication technology to automatically log rehabilitation dosage in people with stroke history, providing an objective and low-burden solution for clinical environments.</p><p><strong>Methods: </strong>This pilot mixed methods study included 2 phases. Phase 1 involved a usability trial with 9 participants conducted at a university research center, assessing usability with the System Usability Scale (SUS) and Intrinsic Motivation Inventory (IMI). Phase 2 consisted of a clinical trial in a National Health Service stroke ward with 15 inpatients, comparing the digital tracker with manual therapist recordings for validity and feasibility using paired t tests, Cohen d, and Bland-Altman plots. An acceptable discrepancy range was set at ±5%-10%.</p><p><strong>Results: </strong>The digital tracker demonstrated high usability with a mean SUS score of 91.43 (SD 9.53) and strong user satisfaction (IMI score 6.29/7, SD 1.50). Clinical trial results showed a strong agreement between the digital and manual methods (t206=-1.60; P=.11; Cohen d=-0.06), with a small mean time discrepancy of 1.23 (SD 11.01) minutes across 207 activities. The Bland-Altman plot indicated good accuracy and consistency between methods, with limits of agreement within the clinically acceptable range.</p><p><strong>Conclusions: </strong>The co-designed digital tracker has been shown to agree with a manual method for recording rehabilitation dosage. This development presents the opportunity for objective, automated, and low-burden recording of rehabilitation dose to support prescription, monitoring, and research.</p>","PeriodicalId":36224,"journal":{"name":"JMIR Rehabilitation and Assistive Technologies","volume":"12 ","pages":"e68129"},"PeriodicalIF":0.0,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12094528/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144081046","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
Machine Learning Clinical Decision Support for Interdisciplinary Multimodal Chronic Musculoskeletal Pain Treatment: Prospective Pilot Study of Patient Assessment and Prognostic Profile Validation. 跨学科多模式慢性肌肉骨骼疼痛治疗的机器学习临床决策支持:患者评估和预后验证的前瞻性试点研究。
Q2 Medicine Pub Date : 2025-05-09 DOI: 10.2196/65890
Fredrick Zmudzki, Rob J E M Smeets, Jan S Groenewegen, Erik van der Graaff

Background: Chronic musculoskeletal pain (CMP) impacts around 20% of people globally, resulting in patients living with pain, fatigue, restricted social and employment capacity, and reduced quality of life. Interdisciplinary multimodal pain treatment (IMPT) programs have been shown to provide positive and sustained outcomes where all other interventions have failed. IMPT programs combined with multidimensional machine learning predictive patient profiles aim to improve clinical decision support and personalized patient assessments, potentially leading to better treatment outcomes.

Objective: We aimed to investigate integrating machine learning with IMPT programs and its potential contribution to clinical decision support and treatment outcomes for patients with CMP.

Methods: This prospective pilot study used a machine learning prognostic patient profile of 7 outcome measures across 4 clinically relevant domains, including activity or disability, pain, fatigue, and quality of life. Prognostic profiles were created for new IMPT patients in the Netherlands in November 2023 (N=17). New summary indicators were developed, including defined categories for positive, negative, and mixed prognostic profiles; an accuracy indicator with high, medium, and low levels based on weighted true- or false-positive values; and an indicator for consistently positive or negative outcomes. The consolidated reporting guidelines checklist for prognostic machine learning modeling studies was completed to provide transparency of data quality, model development methodology, and validation.

Results: The machine learning IMPT prognostic patient profiles demonstrated high accuracy and consistency in predicting patient outcomes. The profile, combined with extended new prognostic summary indicators, provided improved identification of patients with predicted positive, negative, and mixed outcomes, supporting more comprehensive assessment. Overall, 82.4% (14/17) of prognostic patient profiles were consistent with clinician assessments. Notably, clinician case notes indicated the stratified prognostic profiles were directly discussed with around half (8/17, 47.1%) of patients. Clinicians found the prognostic patient profiles helpful in 88.2% (15/17) of initial IMPT assessments to support shared clinician and patient decision-making and discussion of individualized treatment planning.

Conclusions: Machine learning prognostic patient profiles showed promising contributions for IMPT clinical decision support and improving treatment outcomes for patients with CMP. Further research is needed to validate these findings in larger, more diverse populations.

背景:慢性肌肉骨骼疼痛(CMP)影响全球约20%的人,导致患者生活在疼痛、疲劳、社会和就业能力受限以及生活质量下降的环境中。跨学科多模式疼痛治疗(IMPT)方案已被证明提供积极和持续的结果,而所有其他干预措施都失败了。IMPT项目与多维机器学习预测患者档案相结合,旨在改善临床决策支持和个性化患者评估,从而可能带来更好的治疗效果。目的:我们旨在研究机器学习与IMPT程序的整合及其对CMP患者临床决策支持和治疗结果的潜在贡献。方法:这项前瞻性先导研究使用机器学习预测4个临床相关领域的7个结果指标的患者预后概况,包括活动或残疾、疼痛、疲劳和生活质量。我们于2023年11月为荷兰的新IMPT患者创建了预后概况(N=17)。制定了新的摘要指标,包括确定的阳性、阴性和混合预后概况类别;一种基于加权真阳性或假阳性值的具有高、中、低水平的准确度指标;以及一个持续积极或消极结果的指标。完成了预测机器学习建模研究的综合报告指南清单,以提供数据质量、模型开发方法和验证的透明度。结果:机器学习IMPT预后患者资料在预测患者预后方面显示出较高的准确性和一致性。该概况与扩展的新预后汇总指标相结合,可以更好地识别预测阳性、阴性和混合结局的患者,支持更全面的评估。总体而言,82.4%(14/17)的患者预后与临床医生的评估一致。值得注意的是,临床医生的病例记录显示,大约一半(8/17,47.1%)的患者直接讨论了分层预后概况。临床医生发现,在88.2%(15/17)的初始IMPT评估中,患者的预后概况有助于临床医生和患者共同决策和讨论个体化治疗计划。结论:机器学习预后患者档案显示了对IMPT临床决策支持和改善CMP患者治疗结果的有希望的贡献。需要进一步的研究在更大、更多样化的人群中验证这些发现。
{"title":"Machine Learning Clinical Decision Support for Interdisciplinary Multimodal Chronic Musculoskeletal Pain Treatment: Prospective Pilot Study of Patient Assessment and Prognostic Profile Validation.","authors":"Fredrick Zmudzki, Rob J E M Smeets, Jan S Groenewegen, Erik van der Graaff","doi":"10.2196/65890","DOIUrl":"10.2196/65890","url":null,"abstract":"<p><strong>Background: </strong>Chronic musculoskeletal pain (CMP) impacts around 20% of people globally, resulting in patients living with pain, fatigue, restricted social and employment capacity, and reduced quality of life. Interdisciplinary multimodal pain treatment (IMPT) programs have been shown to provide positive and sustained outcomes where all other interventions have failed. IMPT programs combined with multidimensional machine learning predictive patient profiles aim to improve clinical decision support and personalized patient assessments, potentially leading to better treatment outcomes.</p><p><strong>Objective: </strong>We aimed to investigate integrating machine learning with IMPT programs and its potential contribution to clinical decision support and treatment outcomes for patients with CMP.</p><p><strong>Methods: </strong>This prospective pilot study used a machine learning prognostic patient profile of 7 outcome measures across 4 clinically relevant domains, including activity or disability, pain, fatigue, and quality of life. Prognostic profiles were created for new IMPT patients in the Netherlands in November 2023 (N=17). New summary indicators were developed, including defined categories for positive, negative, and mixed prognostic profiles; an accuracy indicator with high, medium, and low levels based on weighted true- or false-positive values; and an indicator for consistently positive or negative outcomes. The consolidated reporting guidelines checklist for prognostic machine learning modeling studies was completed to provide transparency of data quality, model development methodology, and validation.</p><p><strong>Results: </strong>The machine learning IMPT prognostic patient profiles demonstrated high accuracy and consistency in predicting patient outcomes. The profile, combined with extended new prognostic summary indicators, provided improved identification of patients with predicted positive, negative, and mixed outcomes, supporting more comprehensive assessment. Overall, 82.4% (14/17) of prognostic patient profiles were consistent with clinician assessments. Notably, clinician case notes indicated the stratified prognostic profiles were directly discussed with around half (8/17, 47.1%) of patients. Clinicians found the prognostic patient profiles helpful in 88.2% (15/17) of initial IMPT assessments to support shared clinician and patient decision-making and discussion of individualized treatment planning.</p><p><strong>Conclusions: </strong>Machine learning prognostic patient profiles showed promising contributions for IMPT clinical decision support and improving treatment outcomes for patients with CMP. Further research is needed to validate these findings in larger, more diverse populations.</p>","PeriodicalId":36224,"journal":{"name":"JMIR Rehabilitation and Assistive Technologies","volume":"12 ","pages":"e65890"},"PeriodicalIF":0.0,"publicationDate":"2025-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12083736/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144056853","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
Beneficial Effects of the Novel Digital Incentive Spirometer Device and Incentive Spirometer in Patients Undergoing Open-Heart Surgery: Randomized Controlled Trial. 新型数字式激励性肺活量计和激励性肺活量计在心内直视手术患者中的有益效果:随机对照试验。
Q2 Medicine Pub Date : 2025-05-06 DOI: 10.2196/68158
Kornanong Yuenyongchaiwat, Somrudee Harnmanop, Lucksanaporn Mahawong, Nattapoomin Ruangphet, Kannika Jeangubon, Chaopraya Nenmanee, Chitima Kulchanarat, Opas Satdhabudha

Background: The number of patients undergoing open-heart surgery (OHS) is persistently increasing. Additionally, postoperative pulmonary complications have been reported after OHS, and an incentive spirometer has been suggested to prevent postoperative pulmonary complications. However, no commercial incentive spirometer provides the precise inhalation volume. We developed a digital incentive spirometer (DIS) that displays the relevant data.

Objective: In this study, we aimed to explore the beneficial effects of a DIS on respiratory function in patients who underwent OHS.

Methods: A randomized controlled trial was designed with 32 patients scheduled for OHS: 16 individuals each were assigned to the DIS and the flow-oriented incentive spirometer (ie, Triflow incentive spirometer) groups, respectively. The patients were requested to use the DIS and Triflow incentive spirometer 15 times/set, two sets/day, from day 1 to 5 postextubation. All participants underwent lung function and respiratory muscle strength assessments prior to OHS and on day 5 postextubation postoperatively. For comparison between and within the groups, we performed an intention-to-treat analysis with a two-way mixed analysis of variance.

Results: In both the DIS and Triflow incentive spirometer groups, pulmonary function parameters and maximal respiratory pressure were markedly reduced on day 5 postextubation when compared with those prior to OHS (P<.05). There were no significant differences in pulmonary function or respiratory muscle strength between the two groups (P>.05).

Conclusions: Pulmonary function and respiratory muscle strength did not differ significantly between the DIS and Triflow incentive spirometer groups among patients who underwent OHS.

背景:接受心脏直视手术(OHS)的患者数量持续增加。此外,OHS术后肺部并发症也有报道,建议使用激励性肺活量计来预防术后肺部并发症。然而,没有商业激励肺活量计提供精确的吸入量。我们开发了一种显示相关数据的数字激励肺活量计(DIS)。目的:在本研究中,我们旨在探讨DIS对OHS患者呼吸功能的有益影响。方法:设计一项随机对照试验,32例OHS患者,每16例分别被分配到DIS组和流量导向激励肺活量计(即Triflow激励肺活量计)组。要求患者拔管后第1 ~ 5天使用DIS和Triflow激励肺活量计15次/套,2套/天。所有参与者在OHS前和拔管后第5天进行肺功能和呼吸肌力量评估。对于组间和组内的比较,我们使用双向混合方差分析进行意向治疗分析。结果:与OHS前相比,DIS和Triflow刺激肺活计组拔管后第5天肺功能参数和最大呼吸压均显著降低(p < 0.05)。结论:OHS患者的肺功能和呼吸肌力量在DIS和Triflow刺激肺活量计组之间无显著差异。
{"title":"Beneficial Effects of the Novel Digital Incentive Spirometer Device and Incentive Spirometer in Patients Undergoing Open-Heart Surgery: Randomized Controlled Trial.","authors":"Kornanong Yuenyongchaiwat, Somrudee Harnmanop, Lucksanaporn Mahawong, Nattapoomin Ruangphet, Kannika Jeangubon, Chaopraya Nenmanee, Chitima Kulchanarat, Opas Satdhabudha","doi":"10.2196/68158","DOIUrl":"10.2196/68158","url":null,"abstract":"<p><strong>Background: </strong>The number of patients undergoing open-heart surgery (OHS) is persistently increasing. Additionally, postoperative pulmonary complications have been reported after OHS, and an incentive spirometer has been suggested to prevent postoperative pulmonary complications. However, no commercial incentive spirometer provides the precise inhalation volume. We developed a digital incentive spirometer (DIS) that displays the relevant data.</p><p><strong>Objective: </strong>In this study, we aimed to explore the beneficial effects of a DIS on respiratory function in patients who underwent OHS.</p><p><strong>Methods: </strong>A randomized controlled trial was designed with 32 patients scheduled for OHS: 16 individuals each were assigned to the DIS and the flow-oriented incentive spirometer (ie, Triflow incentive spirometer) groups, respectively. The patients were requested to use the DIS and Triflow incentive spirometer 15 times/set, two sets/day, from day 1 to 5 postextubation. All participants underwent lung function and respiratory muscle strength assessments prior to OHS and on day 5 postextubation postoperatively. For comparison between and within the groups, we performed an intention-to-treat analysis with a two-way mixed analysis of variance.</p><p><strong>Results: </strong>In both the DIS and Triflow incentive spirometer groups, pulmonary function parameters and maximal respiratory pressure were markedly reduced on day 5 postextubation when compared with those prior to OHS (P<.05). There were no significant differences in pulmonary function or respiratory muscle strength between the two groups (P>.05).</p><p><strong>Conclusions: </strong>Pulmonary function and respiratory muscle strength did not differ significantly between the DIS and Triflow incentive spirometer groups among patients who underwent OHS.</p>","PeriodicalId":36224,"journal":{"name":"JMIR Rehabilitation and Assistive Technologies","volume":"12 ","pages":"e68158"},"PeriodicalIF":0.0,"publicationDate":"2025-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12074550/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144048387","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
Family Members' Experiences of a Person-Centered Information and Communication Technology-Supported Intervention for Stroke Rehabilitation (F@ce 2.0): Qualitative Analysis. 家庭成员对以人为本的信息通信技术支持的脑卒中康复干预的体验(F@ce 2.0):定性分析。
Q2 Medicine Pub Date : 2025-05-02 DOI: 10.2196/69878
Gunilla Eriksson, Kajsa Söderhielm, Malin Erneby, Susanne Guidetti

Background: Stroke often leads to long-term effects on daily activities and participation. Consequences impact not only stroke survivors but also their close networks, and capturing their experiences is crucial for the development of effective interventions. F@ce 2.0 is a person-centered, information and communication technology (ICT)-supported stroke rehabilitation intervention currently being evaluated.

Objective: This study aims to describe family members' experiences of the F@ce 2.0 intervention from the perspective of being a caregiver to a stroke survivor.

Methods: Participants were family members (n=7) of stroke survivors participating in the intervention. Semistructured interviews were conducted at 2 time points, postintervention and 6 months postbaseline, resulting in a total of 13 interviews. Data was analyzed using qualitative inductive content analysis.

Results: An overarching theme was developed from 4 categories. The main theme was the potential of F@ce 2.0 as a support for family members of stroke survivors in the sudden change of life. The categories were: dialogue and partnership with the F@ce 2.0 team, resuming daily activities lowers the demand for family support, support and involvement through the ICT component of F@ce 2.0, and engagement in F@ce 2.0, leading to suggestions for development.

Conclusions: This study aligns with previous research delineating the effects of stroke on family members of stroke survivors. Participants highlighted the positive impact of the focus on daily activities within the intervention. Furthermore, the ICT component was perceived as a support in structuring rehabilitation. Participants, however, suggested further development, both in terms of content and technology.

背景:中风通常会对日常活动和参与产生长期影响。后果不仅影响中风幸存者,也影响他们的亲密网络,获取他们的经验对于制定有效的干预措施至关重要。F@ce 2.0是一个以人为本,信息和通信技术(ICT)支持的中风康复干预目前正在评估中。目的:本研究旨在从照顾者的角度,描述家庭成员对中风幸存者F@ce 2.0干预的体验。方法:参与者为参与干预的脑卒中幸存者家属(n=7)。在干预后和基线后6个月的2个时间点进行半结构化访谈,共13次访谈。数据分析采用定性归纳内容分析。结果:从4个类别中发展出一个总体主题。这次活动的主题是F@ce 2.0的潜力,它可以帮助中风幸存者的家庭成员应对突发的生活变化。类别为:与F@ce 2.0团队的对话和伙伴关系,恢复日常活动,降低对家庭支持的需求,通过F@ce 2.0的ICT组成部分提供支持和参与,以及参与F@ce 2.0,从而提出发展建议。结论:这项研究与先前关于中风对中风幸存者家庭成员影响的研究一致。与会者强调了在干预措施中注重日常活动的积极影响。此外,信通技术部分被认为是重建结构的一种支助。但是,与会者建议在内容和技术方面进一步发展。
{"title":"Family Members' Experiences of a Person-Centered Information and Communication Technology-Supported Intervention for Stroke Rehabilitation (F@ce 2.0): Qualitative Analysis.","authors":"Gunilla Eriksson, Kajsa Söderhielm, Malin Erneby, Susanne Guidetti","doi":"10.2196/69878","DOIUrl":"https://doi.org/10.2196/69878","url":null,"abstract":"<p><strong>Background: </strong>Stroke often leads to long-term effects on daily activities and participation. Consequences impact not only stroke survivors but also their close networks, and capturing their experiences is crucial for the development of effective interventions. F@ce 2.0 is a person-centered, information and communication technology (ICT)-supported stroke rehabilitation intervention currently being evaluated.</p><p><strong>Objective: </strong>This study aims to describe family members' experiences of the F@ce 2.0 intervention from the perspective of being a caregiver to a stroke survivor.</p><p><strong>Methods: </strong>Participants were family members (n=7) of stroke survivors participating in the intervention. Semistructured interviews were conducted at 2 time points, postintervention and 6 months postbaseline, resulting in a total of 13 interviews. Data was analyzed using qualitative inductive content analysis.</p><p><strong>Results: </strong>An overarching theme was developed from 4 categories. The main theme was the potential of F@ce 2.0 as a support for family members of stroke survivors in the sudden change of life. The categories were: dialogue and partnership with the F@ce 2.0 team, resuming daily activities lowers the demand for family support, support and involvement through the ICT component of F@ce 2.0, and engagement in F@ce 2.0, leading to suggestions for development.</p><p><strong>Conclusions: </strong>This study aligns with previous research delineating the effects of stroke on family members of stroke survivors. Participants highlighted the positive impact of the focus on daily activities within the intervention. Furthermore, the ICT component was perceived as a support in structuring rehabilitation. Participants, however, suggested further development, both in terms of content and technology.</p>","PeriodicalId":36224,"journal":{"name":"JMIR Rehabilitation and Assistive Technologies","volume":"12 ","pages":"e69878"},"PeriodicalIF":0.0,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12064076/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144031733","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
Advances in Infant Cry Paralinguistic Classification-Methods, Implementation, and Applications: Systematic Review. 婴儿哭声副语言分类研究进展综述:方法、实现和应用。
Q2 Medicine Pub Date : 2025-04-29 DOI: 10.2196/69457
Geofrey Owino, Bernard Shibwabo
<p><strong>Background: </strong>Effective communication is essential for human interaction; yet, infants can only express their needs through various types of suggestive cries. Traditional approaches of interpreting infant cries are often subjective, inconsistent, and slow, leaving gaps in timely, precise caregiving responses. A precise interpretation of infant cries can potentially provide valuable insights into the infant's health, needs, and well-being, enabling prompt medical or caregiving actions.</p><p><strong>Objective: </strong>This study seeks to systematically review the advancements in methods, coverage, deployment schemes, and applications of infant cry classification over the last 24 years. The review focuses on the different infant cry classification techniques, feature extraction methods, and practical applications. Furthermore, we aimed to identify recent trends and directions in the field of infant cry signal processing to address both academic and practical needs.</p><p><strong>Methods: </strong>A systematic literature review was conducted using 9 electronic databases: Cochrane Database of Systematic Reviews, JSTOR, Web of Science Core Collection, Scopus, PubMed, ACM, MEDLINE, IEEE Xplore, and Google Scholar. A total of 5904 search results were initially retrieved, with 126 studies meeting the eligibility criteria after screening by 2 independent reviewers. The methodological quality of these studies was assessed using the Cochrane risk of bias tool (version 2; RoB2), with 92% (n=116) of the studies indicating a low risk of bias and 8% (n=10) of the studies showing some concerns regarding bias. The overall quality assessment was performed using TRIPOD (Transparent Reporting of a Multivariable Prediction Model for Individual Prognosis or Diagnosis) guidelines. The data analysis was conducted using R (version 3.64; R Foundation).</p><p><strong>Results: </strong>Notable advancements in infant cry classification methods were realized, particularly from 2019 onward, using machine learning, deep learning, and hybrid approaches. Common audio features included Mel-frequency cepstral coefficients, spectrograms, pitch, duration, intensity, formants, 0-crossing rate, and chroma. Deployment methods included mobile apps and web-based platforms for real-time analysis, with 90% (n=113) of the remaining models remaining undeployed to real-world applications. Denoising techniques and federated learning were limitedly used to enhance model robustness and ensure data confidentiality from 5% (n=6) of the studies. Some of the practical applications spanned health care monitoring, diagnostics, and caregiver support.</p><p><strong>Conclusions: </strong>The evolution of infant cry classification methods has progressed from traditional classical statistical methods to machine learning models but with minimal considerations of data privacy, confidentiality, and ultimate deployment to practical use. Further research is thus proposed to develop standardize
背景:有效的沟通是人类互动的必要条件,然而婴儿只能通过各种类型的暗示性哭声来表达他们的需求。解释婴儿哭声的传统方法往往是主观的,不一致的,并且在及时,精确的护理反应中留下空白。对婴儿哭声的精确解释可以潜在地为婴儿的健康、需求和福祉提供有价值的见解,从而使及时的医疗或护理行动成为可能。目的:本研究旨在系统回顾过去24年来婴儿哭声分类在方法、覆盖范围、部署方案和应用方面的进展。综述了婴儿哭声分类技术、特征提取方法及其在婴儿哭声分类中的应用。此外,我们旨在确定婴儿哭声信号处理领域的最新趋势和方向,以满足学术和实践需求。方法:采用Cochrane system Reviews Database、JSTOR、Web of Science Core Collection、Scopus、PubMed、ACM、MEDLINE、IEEE Xplore、谷歌Scholar等9个电子数据库进行系统文献综述。最初共检索到5904个检索结果,经两名独立审稿人筛选后,有126个研究符合资格标准。使用Cochrane风险偏倚工具第2版(RoB2)评估研究的方法学质量,92% (n=116)的研究显示低偏倚风险,8% (n=10)的研究显示存在偏倚问题。采用TRIPOD(透明报告个体预后或诊断的多变量预测模型)指南进行总体质量评估。使用R 3.64版本进行数据分析。结果:婴儿哭声分类方法取得了显著进展,特别是从2019年开始,采用机器学习、深度学习和混合方法。常见的音频特征包括Mel-frequency倒谱系数(MFCCs),谱图,音高,持续时间,强度,共振峰,过零率和色度。部署方法包括用于实时分析的移动应用程序和基于web的平台,其余90% (n=113)的模型仍未部署到现实世界的应用程序中。从5% (n=6)的研究中,去噪技术和联邦学习被有限地用于增强模型鲁棒性和确保数据机密性。一些实际应用涵盖了医疗保健监控、诊断和护理人员支持。结论:婴儿哭声分类方法的发展已经从传统的经典统计方法发展到机器学习模型,但很少考虑数据的隐私性、保密性,最终部署到实际应用。因此,建议进一步研究开发标准化的基础音频多模态方法,结合更广泛的音频特征,并通过联邦学习等方法确保数据保密性。此外,在特征提取阶段之前,提出了一个初始层用于对哭泣信号进行去噪。这些改进将提高婴儿哭声分类模型在不同医疗环境中的准确性、普遍性和实用性。
{"title":"Advances in Infant Cry Paralinguistic Classification-Methods, Implementation, and Applications: Systematic Review.","authors":"Geofrey Owino, Bernard Shibwabo","doi":"10.2196/69457","DOIUrl":"10.2196/69457","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Effective communication is essential for human interaction; yet, infants can only express their needs through various types of suggestive cries. Traditional approaches of interpreting infant cries are often subjective, inconsistent, and slow, leaving gaps in timely, precise caregiving responses. A precise interpretation of infant cries can potentially provide valuable insights into the infant's health, needs, and well-being, enabling prompt medical or caregiving actions.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;This study seeks to systematically review the advancements in methods, coverage, deployment schemes, and applications of infant cry classification over the last 24 years. The review focuses on the different infant cry classification techniques, feature extraction methods, and practical applications. Furthermore, we aimed to identify recent trends and directions in the field of infant cry signal processing to address both academic and practical needs.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;A systematic literature review was conducted using 9 electronic databases: Cochrane Database of Systematic Reviews, JSTOR, Web of Science Core Collection, Scopus, PubMed, ACM, MEDLINE, IEEE Xplore, and Google Scholar. A total of 5904 search results were initially retrieved, with 126 studies meeting the eligibility criteria after screening by 2 independent reviewers. The methodological quality of these studies was assessed using the Cochrane risk of bias tool (version 2; RoB2), with 92% (n=116) of the studies indicating a low risk of bias and 8% (n=10) of the studies showing some concerns regarding bias. The overall quality assessment was performed using TRIPOD (Transparent Reporting of a Multivariable Prediction Model for Individual Prognosis or Diagnosis) guidelines. The data analysis was conducted using R (version 3.64; R Foundation).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Notable advancements in infant cry classification methods were realized, particularly from 2019 onward, using machine learning, deep learning, and hybrid approaches. Common audio features included Mel-frequency cepstral coefficients, spectrograms, pitch, duration, intensity, formants, 0-crossing rate, and chroma. Deployment methods included mobile apps and web-based platforms for real-time analysis, with 90% (n=113) of the remaining models remaining undeployed to real-world applications. Denoising techniques and federated learning were limitedly used to enhance model robustness and ensure data confidentiality from 5% (n=6) of the studies. Some of the practical applications spanned health care monitoring, diagnostics, and caregiver support.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;The evolution of infant cry classification methods has progressed from traditional classical statistical methods to machine learning models but with minimal considerations of data privacy, confidentiality, and ultimate deployment to practical use. Further research is thus proposed to develop standardize","PeriodicalId":36224,"journal":{"name":"JMIR Rehabilitation and Assistive Technologies","volume":" ","pages":"e69457"},"PeriodicalIF":0.0,"publicationDate":"2025-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12076029/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143754975","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
The Importance of Telerehabilitation and Future Directions for the Field. 远程康复的重要性及未来发展方向。
Q2 Medicine Pub Date : 2025-04-29 DOI: 10.2196/76153
Sarah Munce

During the COVID-19 pandemic, telerehabilitation was critical to providing ongoing care for people with impairments or disabilities, and it remains frequently used and popular after the pandemic. Telerehabilitation has been shown to be feasible and effective in a variety of conditions, including chronic heart failure and coronary artery disease, stroke, multiple sclerosis, and spinal cord injuries, with adverse events being rare. This editorial identifies important areas and future directions for the field, including implementation considerations in the postpandemic context, issues of access and equity, and emerging innovations and personalized care. The development and implementation of this knowledge will ensure that individuals with disabilities and impairments will continue to receive effective, safe, and person-driven care remotely.

在2019冠状病毒病大流行期间,远程康复对于为残障人士提供持续护理至关重要,在大流行之后,远程康复仍然被频繁使用和流行。远程康复已被证明在多种情况下是可行和有效的,包括慢性心力衰竭和冠状动脉疾病、中风、多发性硬化症和脊髓损伤,而且不良事件很少发生。本社论确定了该领域的重要领域和未来方向,包括大流行后背景下的实施考虑、获取和公平问题、新兴创新和个性化护理。这些知识的发展和实施将确保残疾和受损个体将继续获得有效、安全和以人为本的远程护理。
{"title":"The Importance of Telerehabilitation and Future Directions for the Field.","authors":"Sarah Munce","doi":"10.2196/76153","DOIUrl":"10.2196/76153","url":null,"abstract":"<p><p>During the COVID-19 pandemic, telerehabilitation was critical to providing ongoing care for people with impairments or disabilities, and it remains frequently used and popular after the pandemic. Telerehabilitation has been shown to be feasible and effective in a variety of conditions, including chronic heart failure and coronary artery disease, stroke, multiple sclerosis, and spinal cord injuries, with adverse events being rare. This editorial identifies important areas and future directions for the field, including implementation considerations in the postpandemic context, issues of access and equity, and emerging innovations and personalized care. The development and implementation of this knowledge will ensure that individuals with disabilities and impairments will continue to receive effective, safe, and person-driven care remotely.</p>","PeriodicalId":36224,"journal":{"name":"JMIR Rehabilitation and Assistive Technologies","volume":"12 ","pages":"e76153"},"PeriodicalIF":0.0,"publicationDate":"2025-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12076027/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144050960","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
Wheelchair Servicing for Older Adults: Cross-Sectional Study. 老年人轮椅服务:横断面研究。
Q2 Medicine Pub Date : 2025-04-28 DOI: 10.2196/66472
Anand Mhatre, Abigail Dumm, Muyun Zhao, Lorena Parra Rodriguez

Background: Wheelchairs are assistive mobility devices known to experience frequent part failures and breakdowns within 6 months of regular use. No tools or technologies exist to monitor the wheelchairs' condition or usage and inform stakeholders and users regarding when or how often they need to undergo servicing to avoid critical part failure.

Objective: We aimed to test the association between wheelchair usage and manual wheelchair damage, part failures, and consequences for older wheelchair users and evaluate their preferences for a new wheelchair servicing technology.

Methods: A cross-sectional study was performed with older manual wheelchair users atInstituto Nacional de Geriatría in Mexico. Demographic data, wheelchair information, failure counts, and preferences for new technology (sensor and smartphone app for servicing) were collected using surveys. Road shocks experienced by the wheelchair were collected for a week using a sensor.

Results: Ten participants (mean [SD] age, 78.8 [11.8] y; 8 female and 2 male) participated. Seven experienced an average (SD) of 2.86 (1.36) self-reported part failures. Road shocks correlated with self-reported loose brake failures (r(8)=0.58, P=.09), the damaged condition of tires (r(8)=0.61, P=.1), and the damaged condition of brakes (r(8)=0.58, P=.099). No consequences were reported. Part failures increased as self-maintenance occurrences increased (r(9)=0.67, P=.04). More than 8 participants responded that they would like to monitor the wheelchair's condition using the new technology and purchase it at an average (SD) price of US $28.95 (18.13).

Conclusions: In this study, the association between wheelchair usage and failures showed that data-driven wheelchair inspection schedules should be determined through a collaborative approach involving researchers and stakeholders in wheelchair repair provision and older adult users. Older adults are interested in using new technology to engage in wheelchair servicing.

背景:轮椅是一种辅助行动装置,已知在正常使用6个月内经常出现零件故障和故障。没有工具或技术来监测轮椅的状况或使用情况,并告知利益相关者和用户何时或多久需要进行维修以避免关键部件故障。目的:我们旨在测试轮椅使用与老年轮椅使用者手动轮椅损坏、部件故障和后果之间的关系,并评估他们对一种新的轮椅维修技术的偏好。方法:在墨西哥国立研究所Geriatría对老年手动轮椅使用者进行横断面研究。通过调查收集了人口统计数据、轮椅信息、故障计数和对新技术(传感器和智能手机应用程序的服务)的偏好。使用传感器收集轮椅经历的道路冲击一周。结果:10名参与者(平均[SD]年龄78.8 [11.8]y;8名女性和2名男性)参加。其中7人自我报告的零件故障平均(SD)为2.86(1.36)。道路冲击与自我报告的松动制动失效(r(8)=0.58, P= 0.09)、轮胎损坏情况(r(8)=0.61, P= 0.1)和制动器损坏情况(r(8)=0.58, P= 0.099)相关。没有结果报告。部件故障随着自我维修次数的增加而增加(r(9)=0.67, P= 0.04)。超过8名参与者回应说,他们想用新技术监测轮椅的状况,并以28.95美元(18.13美元)的平均价格购买。结论:在本研究中,轮椅使用与故障之间的关系表明,数据驱动的轮椅检查时间表应该通过涉及轮椅维修提供的研究人员和利益相关者以及老年成人用户的合作方式来确定。老年人对使用新技术从事轮椅服务很感兴趣。
{"title":"Wheelchair Servicing for Older Adults: Cross-Sectional Study.","authors":"Anand Mhatre, Abigail Dumm, Muyun Zhao, Lorena Parra Rodriguez","doi":"10.2196/66472","DOIUrl":"https://doi.org/10.2196/66472","url":null,"abstract":"<p><strong>Background: </strong>Wheelchairs are assistive mobility devices known to experience frequent part failures and breakdowns within 6 months of regular use. No tools or technologies exist to monitor the wheelchairs' condition or usage and inform stakeholders and users regarding when or how often they need to undergo servicing to avoid critical part failure.</p><p><strong>Objective: </strong>We aimed to test the association between wheelchair usage and manual wheelchair damage, part failures, and consequences for older wheelchair users and evaluate their preferences for a new wheelchair servicing technology.</p><p><strong>Methods: </strong>A cross-sectional study was performed with older manual wheelchair users atInstituto Nacional de Geriatría in Mexico. Demographic data, wheelchair information, failure counts, and preferences for new technology (sensor and smartphone app for servicing) were collected using surveys. Road shocks experienced by the wheelchair were collected for a week using a sensor.</p><p><strong>Results: </strong>Ten participants (mean [SD] age, 78.8 [11.8] y; 8 female and 2 male) participated. Seven experienced an average (SD) of 2.86 (1.36) self-reported part failures. Road shocks correlated with self-reported loose brake failures (r(8)=0.58, P=.09), the damaged condition of tires (r(8)=0.61, P=.1), and the damaged condition of brakes (r(8)=0.58, P=.099). No consequences were reported. Part failures increased as self-maintenance occurrences increased (r(9)=0.67, P=.04). More than 8 participants responded that they would like to monitor the wheelchair's condition using the new technology and purchase it at an average (SD) price of US $28.95 (18.13).</p><p><strong>Conclusions: </strong>In this study, the association between wheelchair usage and failures showed that data-driven wheelchair inspection schedules should be determined through a collaborative approach involving researchers and stakeholders in wheelchair repair provision and older adult users. Older adults are interested in using new technology to engage in wheelchair servicing.</p>","PeriodicalId":36224,"journal":{"name":"JMIR Rehabilitation and Assistive Technologies","volume":"12 ","pages":"e66472"},"PeriodicalIF":0.0,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12052218/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144019917","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
Mainstream Smart Home Technology-Based Intervention to Enhance Functional Independence in Individuals With Complex Physical Disabilities: Single-Group Pre-Post Feasibility Study. 基于主流智能家居技术的干预提高复杂肢体残疾个体的功能独立性:单组前后可行性研究
Q2 Medicine Pub Date : 2025-04-24 DOI: 10.2196/70855
Dan Ding, Lindsey Morris, Gina Novario, Andrea Fairman, Kacey Roehrich, Palma Foschi Walko, Jessica Boateng
<p><strong>Background: </strong>Mainstream smart home technologies (MSHTs), such as home automation devices and smart speakers, are becoming more powerful, affordable, and integrated into daily life. While not designed for individuals with disabilities, MSHT has the potential to serve as assistive technology to enhance their independence and participation.</p><p><strong>Objective: </strong>The study aims to describe a comprehensive MSHT-based intervention named ASSIST (Autonomy, Safety, and Social Integration via Smart Technologies) and evaluate its feasibility in enhancing the functional independence of individuals with complex physical disabilities.</p><p><strong>Methods: </strong>ASSIST is a time-limited intervention with a design based on the human activity assistive technology model, emphasizing client-centered goals and prioritizing individual needs. The intervention follows a structured assistive technology service delivery process that includes 2 assessment sessions to determine technology recommendations, installation and setup of the recommended technology, and up to 8 training sessions. An occupational therapist led the intervention, supported by a contractor and a technologist. Feasibility was evaluated through several measures: (1) the ASSIST Functional Performance Index, which quantifies the number of tasks transitioned from requiring assistance to independent completion and from higher levels of assistance or effort to lower levels; (2) pre- and postintervention measures of perceived task performance and satisfaction using a 10-point scale; (3) the number and types of tasks successfully addressed, along with the costs of devices and installation services; and (4) training effectiveness using the Goal Attainment Scale (GAS).</p><p><strong>Results: </strong>In total, 17 powered wheelchair users with complex physical disabilities completed the study with 100% session attendance. Across participants, 127 tasks were addressed, with 2 to 10 tasks at an average cost of US $3308 (SD US $1192) per participant. Of these tasks, 95 (74.8%) transitioned from requiring partial or complete assistance to independent completion, while 24 (18.9%) either improved from requiring complete to partial assistance or, if originally performed independently, required reduced effort. Only 8 (6.3%) tasks showed no changes. All training goals, except for 2, were achieved at or above the expected level, with a baseline average GAS score of 22.6 (SD 3.5) and a posttraining average GAS score of 77.2 (SD 4.5). Perceived task performance and satisfaction showed significant improvement, with performance score increasing from a baseline mean of 2.6 (SD 1.2) to 8.8 (SD 1.0; P<.001) and satisfaction score rising from an average of 2.9 (SD 1.3) to 9.0 (SD 0.9; P<.001).</p><p><strong>Conclusions: </strong>The ASSIST intervention demonstrated the immediate benefits of enhancing functional independence and satisfaction with MSHT among individuals with complex physical disab
背景:主流智能家居技术(msht),如家庭自动化设备和智能扬声器,正变得越来越强大,价格实惠,并融入日常生活。虽然不是为残疾人设计的,但MSHT有可能作为辅助技术来增强他们的独立性和参与度。目的:本研究旨在描述一种基于msht的综合干预措施,名为ASSIST(自主性、安全性和社会整合通过智能技术),并评估其在增强复杂身体残疾个体功能独立性方面的可行性。方法:ASSIST是一种基于人类活动辅助技术模型设计的限时干预,强调以客户为中心的目标和优先考虑个人需求。干预遵循结构化的辅助技术服务交付过程,其中包括2次评估会议,以确定技术建议,建议技术的安装和设置,以及多达8次培训会议。在一名承包商和一名技术专家的支持下,一名职业治疗师领导了这次干预。可行性通过以下几个指标进行评估:(1)ASSIST功能绩效指数(ASSIST Functional Performance Index),该指数量化了从需要协助到独立完成、从较高水平的协助或努力到较低水平的任务的数量;(2)采用10分制测量干预前后的感知任务绩效和满意度;(3)成功解决的任务的数量和类型,以及设备和安装服务的成本;(4)利用目标实现量表(GAS)评估培训效果。结果:总共有17名患有复杂身体残疾的电动轮椅使用者以100%的出勤率完成了研究。在所有参与者中,解决了127项任务,其中2至10项任务的平均成本为每位参与者3308美元(1192美元)。在这些任务中,95个(74.8%)从需要部分或完全协助过渡到独立完成,而24个(18.9%)从需要完全或部分协助改进到部分协助,或者如果最初独立执行,则需要减少工作量。只有8个(6.3%)任务没有变化。除2外,所有训练目标均达到或高于预期水平,基线平均GAS评分为22.6 (SD 3.5),训练后平均GAS评分为77.2 (SD 4.5)。感知任务绩效和满意度有显著改善,绩效得分从基线平均值2.6 (SD 1.2)增加到8.8 (SD 1.0);结论:ASSIST干预在增强复杂肢体残疾患者的功能独立性和MSHT满意度方面显示了直接的益处。虽然MSHT有望以较低的成本解决日常生活需求,但诸如数字素养、设备设置和护理人员参与等障碍仍然存在。未来的工作应侧重于可扩展模型、护理人员参与和现实世界实施的可持续解决方案。
{"title":"Mainstream Smart Home Technology-Based Intervention to Enhance Functional Independence in Individuals With Complex Physical Disabilities: Single-Group Pre-Post Feasibility Study.","authors":"Dan Ding, Lindsey Morris, Gina Novario, Andrea Fairman, Kacey Roehrich, Palma Foschi Walko, Jessica Boateng","doi":"10.2196/70855","DOIUrl":"https://doi.org/10.2196/70855","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Mainstream smart home technologies (MSHTs), such as home automation devices and smart speakers, are becoming more powerful, affordable, and integrated into daily life. While not designed for individuals with disabilities, MSHT has the potential to serve as assistive technology to enhance their independence and participation.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;The study aims to describe a comprehensive MSHT-based intervention named ASSIST (Autonomy, Safety, and Social Integration via Smart Technologies) and evaluate its feasibility in enhancing the functional independence of individuals with complex physical disabilities.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;ASSIST is a time-limited intervention with a design based on the human activity assistive technology model, emphasizing client-centered goals and prioritizing individual needs. The intervention follows a structured assistive technology service delivery process that includes 2 assessment sessions to determine technology recommendations, installation and setup of the recommended technology, and up to 8 training sessions. An occupational therapist led the intervention, supported by a contractor and a technologist. Feasibility was evaluated through several measures: (1) the ASSIST Functional Performance Index, which quantifies the number of tasks transitioned from requiring assistance to independent completion and from higher levels of assistance or effort to lower levels; (2) pre- and postintervention measures of perceived task performance and satisfaction using a 10-point scale; (3) the number and types of tasks successfully addressed, along with the costs of devices and installation services; and (4) training effectiveness using the Goal Attainment Scale (GAS).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;In total, 17 powered wheelchair users with complex physical disabilities completed the study with 100% session attendance. Across participants, 127 tasks were addressed, with 2 to 10 tasks at an average cost of US $3308 (SD US $1192) per participant. Of these tasks, 95 (74.8%) transitioned from requiring partial or complete assistance to independent completion, while 24 (18.9%) either improved from requiring complete to partial assistance or, if originally performed independently, required reduced effort. Only 8 (6.3%) tasks showed no changes. All training goals, except for 2, were achieved at or above the expected level, with a baseline average GAS score of 22.6 (SD 3.5) and a posttraining average GAS score of 77.2 (SD 4.5). Perceived task performance and satisfaction showed significant improvement, with performance score increasing from a baseline mean of 2.6 (SD 1.2) to 8.8 (SD 1.0; P&lt;.001) and satisfaction score rising from an average of 2.9 (SD 1.3) to 9.0 (SD 0.9; P&lt;.001).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;The ASSIST intervention demonstrated the immediate benefits of enhancing functional independence and satisfaction with MSHT among individuals with complex physical disab","PeriodicalId":36224,"journal":{"name":"JMIR Rehabilitation and Assistive Technologies","volume":"12 ","pages":"e70855"},"PeriodicalIF":0.0,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12062758/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144015450","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
期刊
JMIR Rehabilitation and Assistive Technologies
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1