Ankle Tracking Training in Stroke
- Conditions
- Stroke
- Interventions
- Behavioral: ankle tracking training
- Registration Number
- NCT01298583
- Lead Sponsor
- University of Minnesota
- Brief Summary
The purpose of this study is to compare the improvement in ankle control and brain activation in subjects with stroke resulting from two different forms of telerehabilitation: tracking training, emphasizing accurate movements, versus movement training, involving simple movements.
Hypotheses:
1. The Track group will show greater improvement in ankle range of motion compared to the Move group.
2. The Track group will show greater improvement in ankle tracking accuracy and greater changes in fMRI (increase in relative volume of activation for ipsilesional sensorimotor cortex, increase in laterality index, and decrease in blood-oxygen-level-dependent (BOLD) signal intensity index) compared to Move group.
3. The Track group will show greater improvement in tracking accuracy at an untrained joint (knee) compared to the Move group.
4. The Track group will show greater improvement in standing balance.
5. The Track group will show greater improvement in walking speed and ankle dorsiflexion during gait compared to the Move group.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 16
- Single stroke with an ischemic infarct.
- Between 18 and 85 years of age.
- Time since stroke onset must be >6 months.
- Cannot be receiving any rehabilitation therapy.
- Impaired ankle dorsiflexion/plantarflexion but at least 10 degrees of active motion.
- Cognition level must be at least 24 out of 30 on the Mini-Mental Examination 7. Able to ambulate at least 100 feet independently. training.
- Cannot have any neuromuscular disorder other than stroke that impairs ankle motion.
- Cannot have an executive function score on Stroop Interference Test of <37.
- Cannot have a score on the Beck Depression Inventory of >10.
- Cannot have ataxia, apraxia, receptive aphasia, hemi-neglect, or severe visual field cut .
- Cannot be pregnant nor have indwelling metal or medical devices incompatible with fMRI.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description ankle tracking ankle tracking training subjects track a target with ankle movement
- Primary Outcome Measures
Name Time Method ankle range of motion Measurement at pretest, posttest and followup
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University of Minnesota
🇺🇸Minneapolis, Minnesota, United States