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Testing Adaptive Physical Activity in Stroke

Not Applicable
Conditions
Stroke
Registration Number
NCT01042990
Lead Sponsor
Baltimore VA Medical Center
Brief Summary

"Testing Adaptive Physical Activity in Stroke" tests the idea that adaptive physical activity (APA) will improve fitness, balance and walking function, daily step activity, and outcomes related to quality of life in individuals with chronic stroke. Adaptive physical activity is an exercise model that combines aerobic exercise with balance and gait training in a socially reinforcing group setting. Individualized homework assignments encourage integration of exercise into daily life routines. Our specific aims are:

1. to determine whether APA improves cardiovascular fitness and metabolic health

2. to measure the effects of APA on gait and balance, ambulatory activity, and ADL function

3. to determine whether APA affects self-reported outcomes related to self-efficacy, fatigue, and stroke-specific quality of life

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
54
Inclusion Criteria
  1. Ischemic stroke greater than or equal to 6 months prior in men or women ages 40- or older. Hemorrhagic stroke greater than or equal to one year prior in men or women ages 40-or older.
  2. Residual hemiparetic gait deficits.
  3. Already completed all conventional inpatient and outpatient physical therapy.
  4. Adequate language and neurocognitive function to participate in exercise testing and training (specific screening instruments used.)
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
VO2 Peakbaseline, 3 months, 6 months, and 3 months post-intervention
Berg Balance Scalebaseline, 3 months, 6 months, and 3 months post-intervention
Dynamic Gait IndexBaseline, 3 months, 6 months, and 3 months post intervention
Step Activity MonitoringBaseline, 3 months, 6 months, and 3 months post-intervention
6 Minute WalksBaseline, 3 months, 6 months, and 3 months post-intervention
Secondary Outcome Measures
NameTimeMethod
Psychosocial questionnairesbaseline, 3 months, 6 months, and 3 months post-intervention

Trial Locations

Locations (1)

Baltimore VAMC

🇺🇸

Baltimore, Maryland, United States

Baltimore VAMC
🇺🇸Baltimore, Maryland, United States
Kathleen M Michael, PhD
Principal Investigator
Marianne Shauhgnessy, PhD
Sub Investigator
Peter Normandt, MS
Sub Investigator
Richard F Macko, MD
Principal Investigator
Andrew P Goldberg, MD
Sub Investigator

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