CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 61 enrolled
Drug / intervention
real stimulation +1 moredevice
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/NCT04569123
NCT04569123N/ACompleted
CompareCT.gov

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

Medical University of South Carolina·interventional·Posted Sep 29, 2020·Updated Feb 9, 2026

In Brief

A clinical study evaluating real stimulation and No stimulation for Stroke and Physical Disability. Completed, enrolled 61 participants across 1 site.

Detailed Summary

The objective of this study is to determine if combining vibration with hand task practice is superior to hand task practice alone.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsStroke, Physical Disability
CountriesUnited States
CollaboratorsEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedSep 29, 2020
Enrollment StartNov 2, 2020
Primary CompletionJan 6, 2025
Study CompletionJan 13, 2025
TodayJul 2, 2026
Enrollment to primary: 4.2 yearsPosted 5.8 years ago

Interventions

real stimulationdevice

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.

No stimulationdevice

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.