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Reshaping Exercise Habits and Beliefs (REHAB)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Department of Veterans Affairs
ClinicalTrials.gov Identifier:
NCT00431821
First received: February 2, 2007
Last updated: July 18, 2013
Last verified: July 2013

February 2, 2007
July 18, 2013
October 2006
February 2011   (final data collection date for primary outcome measure)
Ambulatory Activity Profile [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • 12 weeks and 24 weeks
  • Self-efficacy and outcome expectations (measured
  • by psychosocial questionnaires) at 6 weeks,
Complete list of historical versions of study NCT00431821 on ClinicalTrials.gov Archive Site
Not Provided
  • Functional measures (ie. 30-foot timed walk and
  • Step Activity Monitoring (SAM)
Not Provided
Not Provided
 
Reshaping Exercise Habits and Beliefs (REHAB)
Reshaping Exercise Habits and Beliefs (REHAB): Pilot Testing of a Behavioral Intervention to Improve Mobility After Stroke

Regular exercise has been demonstrated to improve muscle strength, balance, coordination as well as improve cardiovascular fitness levels and overall quality of life in stroke survivors. This study is designed to test the feasibility and effectiveness of a 12-week intervention to education and encourage stroke survivors to exercise following discharge from rehabilitation settings using a walking program and targeted functional activity homework.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
  • Cerebrovascular Accident
  • Stroke
  • Behavioral: Exercise
    Home-based exercise prescriptions with weekly motivational telephone calls.
  • Other: Stroke education
    Stroke education program with matched attention phone calls
  • Arm 1
    Home-based exercise prescriptions with weekly motivational telephone calls.
    Intervention: Behavioral: Exercise
  • Arm 2
    Stroke education program with matched attention phone calls
    Intervention: Other: Stroke education
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
90
October 2012
February 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. 40-85 years old ischemic Stroke patients,
  2. Stroke onset <90 days at enrollment,
  3. Hemiparetic gait disorder,
  4. Patients able to walk 30ft with or w/out assistive device,
  5. Sufficient English comprehension to understand instructions, provide consent, and answer questions,
  6. Lives within 30 miles of the Greater Baltimore area.

Exclusion Criteria:

  1. Dementia (extended MMSE <85 or <80 if education level below 9th grade),
  2. Untreated major clinical depression (CES-D>16) and confirmed with clinical interview,
  3. Heavy alcohol use (<3 oz liquor, 3, 4-oz glasses of wine, or 3, 12- oz beers daily),
  4. Active cancer, or any illness with a life expectancy of less than 6 months,
  5. Any condition in which exercise activity would be contraindicated including, but not limited to: unstable angina, cardiac ischemic event within the past 6 months, congestive heart failure (Stage III or IV), major orthopedic chronic pain or non-stroke neuromuscular disorders restricting exercise, oxygen-dependent COPD or peripheral neuropathy.
Both
40 Years to 85 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00431821
H24242
Yes
Department of Veterans Affairs
Department of Veterans Affairs
Not Provided
Principal Investigator: Marianne Shaughnessy, RN PhD Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD
Department of Veterans Affairs
July 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP