Developing Effectiveness Evaluation and Therapeutic Programs of Rehabilitation
Developing Clinic-oriented Quantitative Effectiveness Evaluation and Individualized Therapeutic Programs of Rehabilitation
1 other identifier
observational
40
1 country
1
Brief Summary
Using robotics, sensors, and sEMG to develop clinic-oriented quantitative effectiveness evaluation and individualized programs of rehabilitation
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jun 2019
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 5, 2019
CompletedStudy Start
First participant enrolled
June 5, 2019
CompletedFirst Posted
Study publicly available on registry
June 7, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
May 23, 2025
May 1, 2025
7.5 years
June 5, 2019
May 20, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Motor function assessment
Fugl-Meyer Assessment
Change from Baseline scores at 1 month
Secondary Outcomes (2)
surface EMG
Change from Baseline status at 1 month
Kinematics test
Change from Baseline status at 1 month
Study Arms (3)
Heahlthy people
perform motor function assessment by using scales, sEMG, and inertia sensors
People with motor deficits
perform motor function assessment by using scales, sEMG, and inertia sensors
Patients with dysphagia
perform motor function assessment by using scales, sEMG, and inertia sensors
Interventions
perform motor function assessment by using scales, sEMG, and inertia sensors
Eligibility Criteria
Recruiting with advertising
You may qualify if:
- no history of psychological/psychotic problems, no history of important diseases.
You may not qualify if:
- history of psychological/psychotic problems
- patients with motor function impairment such as post stroke hemiplegia.
- cognitively or physically unable to cooperate with the examiner to finish the test
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Research Center for Rehabilitation Technical Aids
Beijing, 100176, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
PX Wei, PhD
National Research Center for Rehabilitation Technical Aids
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Director
Study Record Dates
First Submitted
June 5, 2019
First Posted
June 7, 2019
Study Start
June 5, 2019
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 31, 2026
Last Updated
May 23, 2025
Record last verified: 2025-05