COMPLETED

Rehabilitation Device for Hand Mirror Therapy

Conditions

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

This study is a randomized and open comparative study that uses two parallel groups: a control group training with conventional therapy and another group that trains with the device "Miraπ". The participants are patients with stroke with motor weakness in one hand. Two measurement visits are required. During those visits, different hand function assessments will be carried out to analyze the motor function of the subjects hand. The measurements will be done during their inpatient rehabilitation stay, one at time of admission and the second at discharge, each taking 20 minutes. In the time between the measurement visits, the hand therapy takes place fivemtimes a week.

Official Title

Comparative Study on Mirror Therapy With a Rehabilitation Device for Training of Affected Fingers

Quick Facts

Study Start:2024-04-04
Study Completion:2025-04-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06296628

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:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Participants currently accepted and cleared for rehabilitation in the inpatient rehabilitation unit by the rehabilitation medical director.
  2. * Participants with paralysis or motor function problems of only one hand.
  3. * Participants spasticity of the affected hand ( as assessed by by the occupational therapist)
  4. * Participants need mirror therapy because of their health condition.
  5. * Participants are able to memorize easy tasks, and able to follow instructions e.g., moving the healthy fingers.
  1. * Participants who are not cleared physically or medically to participate in standard acute inpatient rehabilitation therapies by the rehabilitation medical director
  2. * Participants who are not able to memorize easy tasks, e.g., moving the healthy fingers.
  3. * Participants with spasticity of the affected hand ( as assed by the occupational therapist)
  4. * Vulnerable populations

Contacts and Locations

Principal Investigator

Rummana Aslam, MD
PRINCIPAL_INVESTIGATOR
Yale University

Study Locations (Sites)

Yale New Haven Health Inpatient Rehabilitation Unit, Bridgeport Hospital
Bridgeport, Connecticut, 06610
United States

Collaborators and Investigators

Sponsor: Yale University

  • Rummana Aslam, MD, PRINCIPAL_INVESTIGATOR, Yale University

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 Date2024-04-04
Study Completion Date2025-04-01

Study Record Updates

Study Start Date2024-04-04
Study Completion Date2025-04-01

Terms related to this study

Additional Relevant MeSH Terms

  • Stroke