CI

At a glance

ClinicalIndex Comparison Record
N/AActive· 120 enrolled
Drug / intervention
Integrated Wearable devices Monitoring sys-Assisted Home Rehabilitation Programdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06410755
NCT06410755N/AActive

Research on Evaluation of Home-based Rehabilitation Monitoring System With Wearable Devices and Self-Report Application

Yonsei University·interventional·Posted May 13, 2024·Updated Apr 29, 2026

In Brief

A clinical study evaluating Integrated Wearable devices Monitoring sys-Assisted Home Rehabilitation Program for Gait Disorders, Neurologic. Active but no longer recruiting, targeting 120 participants across 1 site.

Detailed Summary

The goal of this clinical trial is to evaluate whether monitoring and providing feedback on the performance of a home-based exercise program using an integrated wearable monitoring system improves physical and cognitive function, and activity level in participants with stroke. The integrated wearable monitoring system consists of an insole-type gait analyzer for objective gait assessment, a wrist-worn activity tracker for monitoring daily physical activity, and a self-report mobile application for delivering feedback and collecting participant-reported information. This study also aims to assess participant satisfaction with the integrated wearable monitoring system during a 6-week home-based gait rehabilitation program. The main questions this study aims to answer are: 1. What effect does monitoring and providing feedback using an integrated wearable monitoring system have on physical and cognitive function, and activity level during a home-based gait rehabilitation program? 2. How satisfied are participants with the use of the integrated wearable monitoring system? Researchers will compare an intervention group that receives the integrated wearable monitoring system with a control group that performs the same home-based exercise program without wearable monitoring and feedback. Participants in the intervention group will receive an insole-type gait analyzer, a wrist-worn activity tracker, and access to a mobile application, along with training in a prescribed home-based exercise program. During the 6-week intervention period, participants will wear the insole-type gait analyzer and the activity tracker while performing the home-based exercise program and will use the mobile application to receive feedback and self-report selected daily health-related information. After completion of the 6-week program, the investigators will conduct a satisfaction survey to evaluate participant experience with the integrated wearable monitoring system.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesSouth Korea

Timeline

N/AActive
202520262027
First PostedMay 13, 2024
Enrollment StartMar 12, 2024
Primary CompletionApr 23, 2024
Study CompletionDec 31, 2026
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 2.1 years ago

Interventions

Integrated Wearable devices Monitoring sys-Assisted Home Rehabilitation Programdevice

The researcher provides weekly feedback via telephone to participants in the intervention group based on exercise amount, walking level, and activity data collected through the integrated wearable monitoring system, which includes an insole-type gait analyzer, a wrist-worn activity tracker, and a self-report mobile application. Data collection stability is regularly monitored, and any abnormalities or device-related issues are addressed promptly and documented through telephone communication or in-person visits when necessary.