RECRUITING

Hand Exoskeleton Training Study

Conditions

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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. Participants will use the HandMate device in clinic and in the home. They will also complete clinical upper extremity assessments.

Official Title

Home Training for Upper Limb Stroke Rehabilitation Using a Hand Exoskeleton

Quick Facts

Study Start:2022-01-04

Study Completion:2025-01-31

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06786858

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

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

Inclusion Criteria

Exclusion Criteria

* 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

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

Contacts and Locations

Study Contact

Megan L Grainger

CONTACT

2028771464

megan.l.grainger@medstar.net

Principal Investigator

Pete Lum, PhD

PRINCIPAL_INVESTIGATOR

MedStar RI

Study Locations (Sites)

MedStar National Rehabilitation Hospital

Washington, District of Columbia, 20010

United States

Collaborators and Investigators

Sponsor: Medstar Health Research Institute

Pete Lum, PhD, PRINCIPAL_INVESTIGATOR, MedStar RI

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-01-04

Study Completion Date2025-01-31

Study Record Updates

Study Start Date2022-01-04

Study Completion Date2025-01-31

Terms related to this study

Additional Relevant MeSH Terms

Stroke