Actively Recruiting

Age: 18Years - 80Years
All Genders
Healthy Volunteers
ID03979235

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

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

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

Long-term Monitoring

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

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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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