COMPLETED

Comparing Mirror Therapy Rehabilitation Device to Conventional Mirror Therapy

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Conditions

StrokePainImpaired Motor Function

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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

This is a randomized controlled trial which will compare conventional mirror therapy with mirror therapy using the Miraπ device which physically moves a patient's affected limb. This study will use two parallel groups: (1) receiving conventional mirror therapy as a part of the standard of care as conducted by the participant's clinical care team and (2) receiving mirror therapy with the Miraπ device as conducted by study personnel with the oversight of the participant's clinical care team.

Official Title

Comparing Mirror Therapy Rehabilitation Device to Conventional Mirror Therapy

Quick Facts

Study Start:2025-03-31
Study Completion:2025-08-19
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06842888

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 need mirror therapy because of their health condition.
  4. * Participants' rehabilitation physician determined that mirror therapy would be appropriate for standard of care.
  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. * Minors
  5. * Vulnerable populations

Contacts and Locations

Principal Investigator

Necolle Morgado-Vega
PRINCIPAL_INVESTIGATOR
Yale University

Study Locations (Sites)

Rehabilitation and Wellness Center at the Milford Campus of Bridgeport Hospital
Milford, Connecticut, 06460
United States

Collaborators and Investigators

Sponsor: Yale University

  • Necolle Morgado-Vega, 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 Date2025-03-31
Study Completion Date2025-08-19

Study Record Updates

Study Start Date2025-03-31
Study Completion Date2025-08-19

Terms related to this study

Additional Relevant MeSH Terms

  • Stroke
  • Pain
  • Impaired Motor Function