NCT04569123View on ClinicalTrials.gov

Concomitant Sensory Stimulation During Therapy to Enhance Hand Functional Recovery Post Stroke

NACompletedINTERVENTIONAL
Enrollment

61

Participants

Timeline

Start Date

November 2, 2020

Primary Completion Date

January 6, 2025

Study Completion Date

January 13, 2025

Conditions
StrokePhysical Disability
Interventions
DEVICE

real stimulation

Participants will undergo standardized hand task practice therapy (3 sessions/week for 6 weeks) with the watch worn on the paretic wrist. Participants will be randomized into two groups: The device will deliver vibration for the treatment group.

DEVICE

No stimulation

Participants will undergo standardized hand task practice therapy (3 sessions/week for 6 weeks) with the watch worn on the paretic wrist. Participants will be randomized into two groups: The device will deliver no vibration for the control group during therapy.

Trial Locations (1)

29403

Medical University of South Carolina, Charleston

All Listed Sponsors
collaborator

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

NIH

lead

Medical University of South Carolina

OTHER

NCT04569123 - Concomitant Sensory Stimulation During Therapy to Enhance Hand Functional Recovery Post Stroke | Biotech Hunter | Biotech Hunter