Influence of Timing on Motor Learning
- Conditions
- Cerebrovascular Accident
- Interventions
- Device: Resonating Arm ExerciserOther: Conventional Arm ExerciseOther: Conventional hand exerciseDevice: MusicGlove
- Registration Number
- NCT01769326
- Lead Sponsor
- University of California, Irvine
- Brief Summary
The purpose of this research study is to compare different methods for training hand movement at home after stroke. This study involves research because it will test two experimental devices, the MusicGlove and the Resonating Arm Exerciser (RAE), compared to conventional hand and arm exercises. The MusicGlove is a glove that measures finger movements and allows its user to play a musical computer game using those movements. The RAE is a lever that attaches to a manual wheelchair with elastic bands and can be pushed back and forth to exercise the arm.
- Detailed Description
The purpose of this research study is to compare different methods for training hand movement at home after stroke. This study involves research because it will test two experimental devices, the MusicGlove and the Resonating Arm Exerciser (RAE), compared to conventional hand and arm exercises. The MusicGlove is a glove that measures finger movements and allows its user to play a musical computer game using those movements. The RAE is a lever that attaches to a manual wheelchair with elastic bands and can be pushed back and forth to exercise the arm.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 40
- Age 18 to 80 years of age
- Sustained a single stroke affecting the arm, at least three months prior to enrollment
- Minimal to moderate lost motor control of the arm after stroke
- No active major psychiatric problems, or neurological/orthopedic problems affecting the stroke-affected upper extremity
- No active major neurological disease other than the stroke
- Absence of pain in the stroke-affected upper extremity
- Severe tone at the affected upper extremity
- Severe aphasia
- Severe reduced level of consciousness
- Severe sensory/proprioception deficit at the affected upper extremity
- Currently pregnant
- Difficulty in understanding or complying with instructions
- Inability to perform the experimental task that will be studied
- Increased pain with movement of the stroke-affected upper extremity
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Resonating Arm Exerciser (RAE) Resonating Arm Exerciser Subject participates in 3 weeks of exercising with the experimental device: RAE at a minimum of 3 days per week, 1 hour per day with the exercise program Control Group for RAE Conventional Arm Exercise Subject participates in 3 weeks of conventional arm exercise program, at a minimum of 3 days per week, 1 hour per day with the exercise program. Control Group for Music Glove Conventional hand exercise Subject participates in 3 weeks of conventional hand exercise program, at a minimum of 3 days per week, 1 hour per day with the exercise program. MusicGlove Group MusicGlove Subject participates in 3 weeks of exercising with the experimental device: MusicGlove at a minimum of 3 days per week, 1 hour per day with the exercise program
- Primary Outcome Measures
Name Time Method Motor and Strength Outcome Measure Using Box and Block Test From baseline to 1 month post therapy The primary end point was the change in Box and Blocks score, which measures how many blocks a subject can pick up and place in a box in 60 secons, from baseline to 1 month posttherapy. The higher the scores, the better arm and hand function indicated.
Motor and Strength Outcome Measure Using Fugl-Meyer Score From baseline to 1 month post therapy The primary outcome measure was the change in Upper Extremity FM score on a scale of 0 to 66 at one month post therapy. The higher the scores, the better arm and hand function indicated.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University of California, Irvine
🇺🇸Irvine, California, United States