Comparing Unimanual and Bimanual Mirror Therapy for Upper Limb Recovery Post Stroke
- Conditions
- Cerebral Vascular Accident (CVA)Stroke
- Interventions
- Behavioral: Traditional Home Based Exercise ProgramBehavioral: Bimanual Home Based Mirror Therapy ProgramBehavioral: 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
- 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.
- 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.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Control Group Traditional Home Based Exercise Program Subjects will participate in standard occupational therapy rehabilitation protocol plus a traditional home based exercise program. Experimental Group 2 Bimanual Home Based Mirror Therapy Program Subjects will participate in standard rehabilitation protocol plus bimanual home based mirror therapy program. Experimental Group 1 Unimanual Home Based Mirror Therapy Program Subjects will participate in standard rehabilitation protocol plus unimanual home based mirror therapy program
- Primary Outcome Measures
Name Time Method Grip strength Baseline 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 3.0 Baseline to Six (6) Weeks A subjective standardized 59-items 8 domain questionnaire assessing health status post-stroke.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
New York University School of Medicine
🇺🇸New York, New York, United States