Effects of Two Different Types of Ankle Foot Orthoses on Gait Outcomes in Patients With Subacute Stroke.
Completed · Not applicable
Conditions studied: Stroke, CVA, Hemiplegia, Hemiparesis, Foot Drop
In brief
PURPOSE: The purpose of this study will be to identify whether patients in the subacute stage of stroke, who demonstrate foot drop, will have better gait outcomes when using a Double Adjustable AFO, or a Posterior Leaf Spring AFO. A secondary purpose will be to determine whether one week of practice significantly changes gait outcomes with either of the AFO conditions. INCLUSION CRITERIA: Twenty participants over the age of 18, of any gender and ethnicity, diagnosed with first time unilateral stroke, 4 - 20 weeks post-stroke onset, resulting in hemiparesis with foot drop will be recruited for this study. EXCLUSION CRITERIA: 1. Not able to receive a double adjustable AFO through their insurance 2. Unable to follow two steps commands 3. Unable to ambulate 20 feet with or without assistive device with a minimum level of assistance of contact guard assistance. 4. Cerebellar Stroke 5. Inability to ambulate prior to stroke 6. receiving chemotherapy at the time of study OUTCOME MEASURES: 1. Six Minute walk test 2. Gait Symmetry and Gait velocity measured with GAITRite for self paced velocity walk and fast paced velocity walk. DATA COLLECTION: Data will be collected three times over two weeks period. First Visit: Demographics, Fugl-Meyer Lower Extremity Assessment of sensorimotor function, Mini Mental State Examination 6MWT and GAITRite measurements using Both types of AFO in a random order. Afterwards participant will be given one type of AFO (randomly selected) to practice walking for a week. Second Visit: 6MWT and GAITRite measurements using the type of AFO they were practicing with. Then the other type of AFO will be given to practice walking for a week. Third Visit: 6MWT and GAITRite measurements using the second type of AFO that they were practicing with the week prior. Patient will be asked which type of AFO they prefer to use.
Key facts
- Study ID
- NCT02693834
- Run by
- Texas Woman's University
- People needed
- 23
- Starts
- 2016-01-01
- Expected to finish
- 2018-04-01
- Last updated by the study team
- 2020-02-28
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosed with first time unilateral stroke
- 4 - 20 weeks post-stroke onset
- resulting in hemiparesis with foot drop
You may not qualify if…
- Inability to receive a double adjustable AFO through their insurance
- unable to follow two steps commands
- unable to ambulate 20 feet with or without assistive device with a minimum level of assistance of contact guard assistance
- diagnosis of cerebellar stroke
- non ambulatory prior to stroke onset
Where it is running
- Baylor Institute for rehabilitation — Frisco, Texas, United States
Full record on ClinicalTrials.gov
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