Hand Exoskeleton Training Study

Part of paid clinical trials in Washington D.C., District of Columbia.

Sponsor
Medstar Health Research Institute
Study ID
NCT06786858
Status
Recruiting
Apply to this trial

Conditions

Eligibility Criteria

Sex
ALL
Age
21 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • HandMate — DEVICE
    HandMate device is used for 20 hours in 4 weeks. Device is then used in the home for 3 months at discretion of participant.

Study Details

The goal of this study is to evaluate the HandMATE device's effectiveness in the rehabilitation of stroke patients and asses if the HandMATE application is received well by stroke survivors. Participants will use the HandMate device in clinic and in the home. They will also complete clinical upper extremity assessments.

Key Dates

Start date
Jan 4, 2022
Status verified
Jan 2025
Primary completion
Jan 4, 2024
Completion
Jan 31, 2025

Study Design

Enrollment
15 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER

Arms

  • Experimental: HandMate Use
    HandMate device fitted for a stroke participant.

Primary Outcome Measure

Fugl-Meyer Upper Extremity (FMA-UE) Test [ Time Frame: Change from baseline Fugl-Meyer score at 6 weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
MedStar National Rehabilitation HospitalWashington D.C.District of Columbia20010
Megan L Grainger
[email protected]
202-877-1464

Find similar trials in Washington D.C., DC

By condition
Stroke
By specialty
NeurologyBrain disorders
By research site
MedStar National Rehabilitation Hospital· Washington D.C., DC

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