Clinical Implementation of Multichannel Functional Electrical Stimulation Device for Gait Rehabilitation in Subchronic Stroke: A Feasibility Study

NANot yet recruitingINTERVENTIONAL
Enrollment

5

Participants

Timeline

Start Date

October 31, 2025

Primary Completion Date

September 1, 2026

Study Completion Date

February 28, 2027

Conditions
Stroke SequelaeStroke ( 3 Months After Onset)
Interventions
DEVICE

Multichannel functionnal electrical stimulation

"The participants completed 24 gait rehabilitation sessions over the course of 8 to 12 weeks. Each session lasted between 30 minutes and 1 hour. A minimum of 2 days seperated two consecutive sessions. The number of sessions was used for standardization of the protocol instead of duration of treatment.~Four evaluations were completed throughout the protocol. Baseline evaluation(V1) was completed between 2 and 7 days before the first rehabilitation session. Intermediate evaluation(V2) was completed between 2 and 7 days after the 12th rehabilitation session, in other words 4 to 6 weeks after the baseline evaluation (V1) . Post-treatment evaluation(V3) was completed between 2 and 7 days after the 24th rehabilitation session, in other words 8 to 12 weeks after the baseline evaluation (V1). Follow-up evaluation(V4) was completed 2 months(60 days) after the 24th rehabilitation session, in other words 16 to 20 weeks after the baseline evaluation (V1)."

All Listed Sponsors
collaborator

Kurage SAS

OTHER

collaborator

Natural Sciences and Engineering Research Council, Canada

OTHER

collaborator

Clinique Synapse - Réadaptation & Vie Active

UNKNOWN

lead

TOPMED

OTHER

NCT07211672 - Clinical Implementation of Multichannel Functional Electrical Stimulation Device for Gait Rehabilitation in Subchronic Stroke: A Feasibility Study | Biotech Hunter | Biotech Hunter