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Comparing Unimanual and Bimanual Mirror Therapy for Upper Limb Recovery Post Stroke

Completed
Conditions
Cerebral Vascular Accident (CVA)
Stroke
Interventions
Behavioral: Traditional Home Based Exercise Program
Behavioral: Bimanual Home Based Mirror Therapy Program
Behavioral: Unimanual Home Based Mirror Therapy Program
Registration Number
NCT02780440
Lead Sponsor
NYU Langone Health
Brief Summary

The purpose of this randomized controlled study is to

1. Examine the feasibility of a home Mirror therapy (MT) program in the NYC metropolitan area;

2. Evaluate the effectiveness of home MT versus traditional home exercise program; and

3. Evaluate the superiority of unimanual or bimanual MT intervention protocols for chronic stroke subjects with moderate hand deficits. Subjects from occupational therapy at the Ambulatory Care Center of NYU Langone Center with a diagnosis of cerebral vascular accident (CVA) or stroke will be divided into three (3) groups:

* Control Group subjects will participate in standard occupational therapy rehabilitation protocol plus a traditional home based exercise program.

* Experimental group 1 subjects will participate in standard rehabilitation protocol plus unimanual home based mirror therapy program

* Experimental group 2 subjects will participate in standard rehabilitation protocol plus bimanual home based mirror therapy program.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
22
Inclusion Criteria
  • First time unilateral stroke > 3 months post stroke.
  • Cognitively be able to follow direction
  • Cognitively be able to consent to participation in research study
  • Moderate/severe deficits as per the Fugl-Meyer assessment score from 10-50 and the ability to grasp and release a small towel or washcloth.
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Exclusion Criteria
  • Complex medical problems, that would render the subject unable to participate in an extensive home program
  • History of pre-existing neurological or psychiatric diseases, orthopedic conditions of the upper limbs, or peripheral nerve injuries that render the subject unable to sit or to move either upper limb
  • Hearing and vision impairments which may impede subjects participation in the home program
  • Perceptual deficits such as apraxia, neglect, or agnosias as per clinical evaluation which may impede subjects participation in the home program
  • Botox injection in affected arm/hand within 3 months
  • Global aphasia that may interfere with understanding instruction for testing or home exercise program.
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Control GroupTraditional Home Based Exercise ProgramSubjects will participate in standard occupational therapy rehabilitation protocol plus a traditional home based exercise program.
Experimental Group 2Bimanual Home Based Mirror Therapy ProgramSubjects will participate in standard rehabilitation protocol plus bimanual home based mirror therapy program.
Experimental Group 1Unimanual Home Based Mirror Therapy ProgramSubjects will participate in standard rehabilitation protocol plus unimanual home based mirror therapy program
Primary Outcome Measures
NameTimeMethod
Grip strengthBaseline to Six (6) Weeks

Grip strength is important to measure as it is correlated with stroke recovery.

Action Research Arm Test (ARAT)Baseline to Six (6) Weeks

An interview based tool that measures a subject's perceived difficulty with the use of their arm/hands with activities of daily living post-stroke.

Fugl-Meyer Assessment (FMA)Baseline to Six (6) Weeks

Gold Standard to evaluate and measure recovery in patients with hemiplegia post stroke.

Stroke Impact Scale Version 3.0Baseline to Six (6) Weeks

A subjective standardized 59-items 8 domain questionnaire assessing health status post-stroke.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

New York University School of Medicine

🇺🇸

New York, New York, United States

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