Under construction – not a live service
Sign in
Taking people in United StatesNo phase

Hand Exoskeleton Device Tested for Hand Rehabilitation After Stroke

Tests a hand exoskeleton device at home and clinic for adults recovering from stroke.

Plain-language title generated from the registry record
Registry title: Hand Exoskeleton Training Study

Key facts

Where
Washington D.C., United StatesSee the site

Where in United States

  • MedStar National Rehabilitation HospitalWashington D.C., United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Medstar Health Research Institute
Trial code
NCT06786858
Record updated
22 January 2025
Original description
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.Read full original descriptionShow less

Home Training for Upper Limb Stroke Rehabilitation Using a Hand Exoskeleton

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.

Inclusion: Age of 21 or older; diagnosis of stroke more than 6 months prior confirmed from MRI or CT; voluntary hand activity (score of 1 or more, finger extension item, Fugl-Meyer Test); adequate cognitive status; Impaired ability to open affected hand.

Exclusion: receiving or planning to receive antispasticity medications during enrollment into the study; receiving physical or occupational therapy outside of study protocols; severe sensory loss (2 or more on the sensory item, NIH Stroke Scale/Score); hemispatial neglect; less than full passive range of motion in finger joints; have excessive pain in any joint of the affected extremity that could limit ability to cooperate with the protocols.

ClinicalTrials.gov NCT06786858