CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 53 enrolled
Drug / intervention
A functional electrical stimulation device for post-stroke rehabilitationdevice
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/NCT04154514
NCT04154514N/ACompleted

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

Chinese University of Hong Kong·interventional·Posted Nov 6, 2019·Updated Dec 26, 2025

In Brief

A clinical study evaluating A functional electrical stimulation device for post-stroke rehabilitation for Chronic Stroke. Completed, enrolled 53 participants across 1 site.

Detailed Summary

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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsChronic Stroke
CountriesHong Kong

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedNov 6, 2019
Enrollment StartFeb 1, 2019
Primary CompletionDec 1, 2025
TodayJul 2, 2026
Enrollment to primary: 6.8 yearsPosted 6.7 years ago

Interventions

A functional electrical stimulation device for post-stroke rehabilitationdevice

Most of the FDA-approved commercial FES devices deliver therapy that targets specific kinematic impairment in the step cycle (e.g., foot drop). Our device will be unique in that it can stimulate many muscles around multiple joints for a more comprehensive and naturalistic restoration of lower-limb motor functions.