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NCT04154514Completed

A Potential Wearable for Post-stroke Rehabilitation

A Wearable for Post-stroke Rehabilitative Multi-muscle Stimulation Inspired by the Natural Organization of Neuromuscular Control

Source: ClinicalTrials.gov · Last updated 26 Dec 2025

Brief summary (registry, in English)

Participants are seeking to unleash the full therapeutic potential of a newly developed, customizable and potentially commericializable 10-channel Functional Electrical Stimulation (FES) to rehabilitate the gait of chronic stroke survivors. Each subject will undergo 18-sessions (\~1 month) FES training. Participants will utilize the theory of muscle synergies from motor neurosciences, which are defined as neural modules of motor control that coordinate the spatiotemporal activation patterns of multiple muscles, to guide our personal selections of muscles for FES. It is hypothesized that chronic stroke survivors will learn from FES stimulations, over several daily sessions, both by suppressing the original abnormal muscle synergies and by employing the normal muscle synergies as specified in the FES. It is also expected that the walk synergies of the paretic side of chronic stroke survivors should be more similar to healthy muscle synergies at the two post-training time points than before training.

Status (registry)
Completed
Study type
Interventional
Enrollment
53 (actual)
First submitted
10 Oct 2019
Start date
1 Feb 2019
Primary completion date
1 Dec 2025
Lead sponsor
Chinese University of Hong Kong
Diseases
Stroke
NCT number
NCT04154514

What you commit to

  • Study type: Interventional
  • Participants enrolled: 53
  • From 1 Feb 2019 to the primary completion date, 1 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Have cardiac pacemaker;
  • Patients with type i and ii diabetes

Other

  • Cannot comprehend and follow instructions, or with a score \<21 on the mini-mental state exam;
  • Have skin lesions at the locations where FES or EMG electrodes may be attached;
  • Have major depression;
  • Present with severe neglect

Who the study is looking for

  • Right-handed elderly chronic stroke survivors; age ≥40; ≥6 months post-stroke
  • Unilateral ischemic brain lesions
  • Participants should be able to walk continuously for ≥15 min. with or without assistive aid

Age in the registry: 40 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
The Hong Kong Polytechnic University
Coordinator of this site? Confirm its status
Hong KongHong KongUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.