Skip to main content
Clinical Trials/NCT02917343
NCT02917343
Completed
Not Applicable

Effect of Mirror Therapy and Repetitive Task Training on Upper Extremity Function for Persons With Subacute Stroke

Quinnipiac University0 sites4 target enrollmentOctober 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
Quinnipiac University
Enrollment
4
Primary Endpoint
Change in Patient Specific Functional Scale
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of the study is to determine the effect of a combined mirror therapy and task oriented/repetitive task training on upper extremity function of persons with hemiplegia due to cerebrovascular accident or stroke.

Detailed Description

This case series was designed to to determine the effect of a mirror therapy and repetitive task training program on the weak arm and hand functioning due to the consequences of stroke. Mirror therapy is a type of therapy mirror reflection of the stronger arm and hand helps to promote reorganization of neurons. Studies have shown that mirror therapy is an effective adjunct to regular exercise and task-oriented therapy. To qualify for this study, participants must meet the following criteria: 1) age 21 years or more; 2) first-time stroke with onset of at least 3 months; 3) slight movement of the weaker arm or /and hand; 3) stable physical and mental health; and 4) mentally capable and competent to make health care-related decisions and carry out a home program. Participants were required to come to Quinnipiac University - North Haven campus to undergo mirror therapy training, in 45-60 minute sessions, twice a week for one month. They were also required to complete pre-testing before and post-testing after the mirror therapy program. In addition, they were required to carry-out a home program that includes the use of a mirror box and self-selected tasks. The home program required them to exercise and practice the use of their more affected arm and hand for at least 1-2 hours a day. Participation was strictly voluntary. Participants were informed of the minimal risks involved as well as their options to continue or withdraw from the study upon initial consent. The study did not yield physical or mental harm to the participants.

Registry
clinicaltrials.gov
Start Date
October 2014
End Date
April 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • able to give consent, complete home program
  • minimal arm and hand use with the paretic limb
  • onset of stroke of at least 3 months

Exclusion Criteria

  • \>1 stroke episode
  • significant cognitive and visual perceptual deficit
  • lack of social support

Outcomes

Primary Outcomes

Change in Patient Specific Functional Scale

Time Frame: Change from baseline at 2 months

Patient Specific Functional Scale is a measure that involves self-rating of self-selected functional tasks

Change in Fugl Myer Motor Assessment

Time Frame: Change from baseline at 2 months

Fugl-Meyer Motor Assessment is a clinical performance test of motor ability of the upper extremity

Secondary Outcomes

  • Change in Motor Activity Log(Change from baseline at 2 months)

Similar Trials