Sensory Feedback and Hand Motor Adaptation in Stroke

This study is exploring how different types of visual feedback in a virtual reality (VR) environment can affect hand movement in people who have had a stroke. You would perform hand movements while wearing a head-mounted VR display. The study will test two interventions: "Visual ROM augmentation," where your finger joint movement appears amplified in VR, and "Visual ROM reduction," where it appears reduced. Researchers will measure your joint range of motion (ROM) to see how these visual changes impact your hand movements. The study is looking for 15 people aged 20-70 who have experienced a stroke at least six months ago, with some remaining weakness on one side of their body (hemiparesis) and a specific score on a hand function test (Fugl-Meyer Upper Extremity Section 31-55). It is also recruiting 15 healthy control subjects. People with severe medical illness, hand/arm pain, or complete loss of finger control cannot participate. The current recruitment status is unclear.

Study design
This is an interventional study with 30 planned participants (15 stroke survivors and 15 control subjects). Participants will be randomly assigned to two groups to receive the visual feedback interventions in a different order.
What's involved
You would perform hand movements in a virtual reality environment using a head-mounted display. The study measures your joint range of motion (ROM) at the time of the procedure.
Compensation
Not stated in the trial record.
Follow-up
Not specified.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07598695

Sensory Feedback and Hand Motor Adaptation

Recruiting
EARLY_PHASE1Ages 20–70InterventionalBasic science
The Catholic University of America
~30 participants
Updated 2026-05-22 on ClinicalTrials.gov
What's tested:Visual ROM augmentationVisual ROM reduction

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Joint range of motion (ROM)
Measured over Periprocedural
Stroke

NCT07598695

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Catholic University of America

    Washington D.C., District of Columbiastudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

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Eligibility criteria

Inclusion

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

Exclusion

Presence of concurrent severe medical illness
Pain in hand or arm with movements
Loss of voluntary control of fingers and thumb
Inability to provide informed consent
Musculoskeletal injuries (e.g., fracture) or medical complications (e.g., severe cardiovascular disease).
  • Joint range of motion (ROM)Periprocedural

    range of motion of individual finger joints under each condition, measured by embedded cameras that digitize individual finger segments