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Impact of Altered Sensory Feedback on Adaptation of Hand Muscle Coordination of Stroke Survivors

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Early Phase 1
SUMMARY

The following experiment will be conducted with 15 chronic stroke survivors and 15 control subjects. Subjects will perform hand movements in the virtual reality environment using a head-mounted display. Quest's onboard cameras allow real-time tracking of hand motion, estimating joint angles of the finger and the thumb. For each feedback manipulation condition (i.e., movement amplification or reduction), the estimated joint angles will be multiplied by a factor greater than 1 (amplification) or a factor smaller than 1 (reduction). Then the newly-estimated hand posture will be displayed in the VR environment. Subjects will be randomly assigned into two groups (A and B), who will receive the assistance in a different order. Subjects will perform finger extension under three conditions: no sensory modulation, movement visual feedback (VF) amplification, and movement VF reduction (error augmentation), while their movement muscle activation patterns are recorded.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 20
Maximum Age: 70
Healthy Volunteers: t
View:

• Age: 20 - 70 years old

• First-ever unilateral cortical stroke with resultant hemiparesis at least 6 months prior to the experimental testing

• Fugl-Meyer Upper Extremity Section 31 - 55

Locations
United States
Washington, D.c.
Catholic University of America
RECRUITING
Washington D.c.
Contact Information
Primary
Sang Wook Lee, PhD
leesw@cua.edu
202-319-6218
Time Frame
Start Date: 2025-10-01
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 30
Treatments
Experimental: Visual ROM augmentation followed by visual ROM reduction
Experimental: Visual ROM reduction followed by visual ROM augmentation
Related Therapeutic Areas
Sponsors
Leads: The Catholic University of America
Collaborators: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

This content was sourced from clinicaltrials.gov

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