Actively Recruiting
Developing Clinic-oriented Quantitative Effectiveness Evaluation and Individualized Therapeutic Programs of Rehabilitation
Led by National Research Center for Rehabilitation Technical Aids · Updated on 2025-05-23
40
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying the use of robotics, sensors, and surface electromyography (sEMG) to create clinic-friendly methods for measuring rehabilitation effectiveness and developing personalized rehabilitation programs. This observational study includes healthy volunteers as well as patients with motor deficits and dysphagia, aiming to improve assessment techniques for these groups. Participants undergo motor function assessments using scales, sEMG, and inertia sensors to gather detailed movement and muscle activity data. These assessments are performed across different groups including healthy individuals, those with motor impairments like post-stroke hemiplegia, and patients with swallowing difficulties. During the study, participants' motor function changes are evaluated at one month from baseline using motor assessments, surface EMG, and kinematic tests. The study tracks how these measures change over time to better understand rehabilitation progress. The total participation period includes initial testing and follow-up assessments to monitor motor function improvements or changes.
CONDITIONS
Brief Title
Developing Effectiveness Evaluation and Therapeutic Programs of Rehabilitation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy people with no history of psychological or psychotic problems or important diseases
- Patients with motor function impairments such as post-stroke hemiplegia
- Adults aged 18 to 80 years
- Able to cooperate with examiners to complete motor function assessments
You will not qualify if you...
- Healthy people with a history of psychological or psychotic problems
- Patients who are cognitively or physically unable to cooperate with examiners to complete tests
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 month
Participants undergo motor function assessments using scales, sEMG, and inertia sensors to evaluate their motor function status.
1 baseline visit and 1 follow-up visit
Duration - Up to 1 month after baseline assessment
Participants are observed to monitor changes in motor function after initial assessments.
Additional visits may occur depending on participant condition
Trial Site Locations
Total: 1 location
1
National Research Center for Rehabilitation Technical Aids
Beijing, China, 100176
Actively Recruiting
Research Team
L
LT Wang, PhD
P
PX Wei, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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