Moderate-Intensity Exercise Versus High-Intensity Interval Training to Recover Walking Post-Stroke
Purpose
The objective of this study is to determine the optimal training intensity and the minimum training duration needed to maximize immediate improvements in walking capacity in chronic stroke. A single-blind, phase II, 3-site randomized controlled trial has been planned. Fifty persons >6 months post stroke will randomize to either moderate-intensity aerobic locomotor training or high-intensity interval locomotor training; each for 45 minutes, 3x/week for up to 36 total sessions over approximately 12 weeks. Clinical measures of walking function, aerobic fitness, daily walking activity and quality of life will be assessed at baseline (PRE) and after 4, 8 and 12 weeks of training (POST-4WK, POST-8WK, POST-12WK).
Condition
- Stroke
Eligibility
- Eligible Ages
- Between 40 Years and 80 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Age 40-80 years at time of consenting 2. Single stroke for which participant sought treatment, 6 months to 5 years prior to consent date 3. Walking speed <1.0 m/s on the 10-meter walk test 4. Able to walk 10m over ground with assistive devices as needed and no continuous physical assistance from another person (guarding and intermittent assistance for loss of balance allowed) 5. Able to walk at least 3 minutes on the treadmill at ≥0.13m/s (0.3 mph) 6. Stable cardiovascular condition (AHA class B, allowing for aerobic capacity <6 metabolic equivalents) 7. Able to communicate with investigators, follow a 2-step command and correctly answer consent comprehension questions
Exclusion Criteria
- Exercise testing uninterpretable for ischemia or arrhythmia (e.g. resting ECG abnormality that makes exercise ECG uninterpretable for ischemia and no other clinical testing from the past year available to rule out) 2. Evidence of significant arrhythmia or myocardial ischemia on treadmill ECG graded exercise test in the absence of recent (past year) more definitive clinical testing (e.g. stress nuclear imaging) with negative result 3. Hospitalization for cardiac or pulmonary disease within past 3 months 4. Implanted pacemaker or defibrillator 5. Significant ataxia or neglect (score of 2 on NIH stroke scale item 7 or 11) 6. Severe lower limb spasticity (Ashworth >2) 7. Recent history (<3 months) of illicit drug or alcohol abuse or significant mental illness 8. Major post-stroke depression (Patient Health Questionnaire [PHQ-9] ≥ 10) in the absence of depression management by a health care provider 9. Currently participating in physical therapy or another interventional study 10. Recent botulinum toxin injection to the paretic lower limb (<3 months) or planning to have lower limb botulinum toxin injection in the next 4 months 11. Foot drop or lower limb joint instability without adequate stabilizing device, as assessed by a physical therapist 12. Clinically significant neurologic disorder other than stroke or unable to walk outside the home prior to stroke 13. Other significant medical condition likely to limit improvement or jeopardize safety as assessed by a physical therapist (e.g. joint contracture, gait limited by pain) 14. Pregnancy 15. Previous exposure to fast treadmill walking (>3 cumulative hours) during clinical or research therapy in the past year
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Treatment
- Masking
- Single (Outcomes Assessor)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Active Comparator Moderate-Intensity Aerobic Training |
|
|
|
Experimental High-Intensity Interval Training |
|
More Details
- Status
- Completed
- Sponsor
- University of Cincinnati