RECRUITING

R3THA Rehabilitation Feasibility and Usability Study

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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 purpose of this study is to assess how the Rehabilitation Technologies for Hand and Arm (R3THA) device can be used for rehabilitation of people with stroke. the study will evaluate the feasibility of R3THA as outpatient telerehabilitation administered by trained clinicians to individuals with stroke.

Official Title

R3THA Rehabilitation Feasibility and Usability Study

Quick Facts

Study Start:2024-03-27

Study Completion:2026-03-25

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06854978

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:20 Years to 80 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. must be between the ages of 20 and 80 2. must have enough movement in my arms and hands to actively interact with the video games as determined by study staff 3. must have internet access at home. 4. must be comfortable performing basic functions on a computer, such as browsing the internet. 5. must be able to sit without a loss of balance while performing activities with my arms and hands as determined by study staff.	Pregnancy or breastfeeding Severe psychiatric disorders Active substance abuse Unstable medical conditions Inability to comply with study requirements

Inclusion Criteria

Exclusion Criteria

1. must be between the ages of 20 and 80
2. must have enough movement in my arms and hands to actively interact with the video games as determined by study staff
3. must have internet access at home.
4. must be comfortable performing basic functions on a computer, such as browsing the internet.
5. must be able to sit without a loss of balance while performing activities with my arms and hands as determined by study staff.

Pregnancy or breastfeeding
Severe psychiatric disorders
Active substance abuse
Unstable medical conditions
Inability to comply with study requirements

Contacts and Locations

Study Contact

Kiran Karunakaran, PhD

CONTACT

973-324-3590

kkarunakaran@kesslerfoundation.org

Principal Investigator

Kiran Karunakaran, PhD

PRINCIPAL_INVESTIGATOR

Kessler Foundation

Study Locations (Sites)

Kessler Foundation

West Orange, New Jersey, 07052

United States

Collaborators and Investigators

Sponsor: Kessler Foundation

Kiran Karunakaran, PhD, PRINCIPAL_INVESTIGATOR, Kessler Foundation

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 Date2024-03-27

Study Completion Date2026-03-25

Study Record Updates

Study Start Date2024-03-27

Study Completion Date2026-03-25

Terms related to this study

Additional Relevant MeSH Terms

Stroke