ClinicalTrials.gov
ClinicalTrials.gov Menu

Early Aerobic Training Program After Ischemic Stroke

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00248222
Recruitment Status : Completed
First Posted : November 3, 2005
Last Update Posted : October 27, 2009
Sponsor:
Information provided by:
Sheba Medical Center

November 2, 2005
November 3, 2005
October 27, 2009
October 2005
June 2009   (Final data collection date for primary outcome measure)
  • 6 Minute Walk Test at 6 weeks
  • Modified Bruce Exercise Test at 6 weeks
  • Activity by Ankle accelerometer at 6 weeks
Same as current
Complete list of historical versions of study NCT00248222 on ClinicalTrials.gov Archive Site
  • Recurrent vascular events at 6 weeks
  • METS at 6 weeks
  • Stair climbing ascend and descend test at 6 weeks
  • Four Square Step Test at 6 weeks
  • Gait symmetry by SmartStep at 6 weeks
  • Walking Impairment Questionnaire at 6 weeks
  • Rivermead Mobility Index at 6 weeks
  • Similar outcome measures 3 months later
Same as current
Not Provided
Not Provided
 
Early Aerobic Training Program After Ischemic Stroke
Not Provided
The purpose of this study is to examine the feasibility and efficacy of an early supervised aerobic exercise program for patients following a minor ischemic stroke.
The purpose of this study is to examine the feasibility and efficacy of an early supervised aerobic exercise program for patients following a minor ischemic stroke. Patients after a minor ischemic stroke would be randomized within 1-3 weeks of stroke onset to a control group (6 weeks of low intensity stretching and coordination exercises followed by a supervised aerobic training program) or an experimental group (immediate aerobic training program). Patients will be evaluated for measures of ambulation endurance, mobility, gait, functional assessment and clinical follow-up after 6 weeks and again 3 months later.
Interventional
Phase 2
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
  • Stroke
  • Cerebrovascular Accident
Behavioral: Supervised aerobic training
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
Not Provided
Not Provided
June 2009
June 2009   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • minor ischemic stroke

Exclusion Criteria:

  • unstable angina
  • severe lung disease
  • severe symptomatic peripheral vascular disease
  • dementia or other severe neurological disease
  • other severe uncontrolled medical problem
Sexes Eligible for Study: All
18 Years to 80 Years   (Adult, Older Adult)
No
Contact information is only displayed when the study is recruiting subjects
Israel
 
 
NCT00248222
SHEBA-05-3840-DT-CTIL
No
Not Provided
Not Provided
Prof. David Tanne, Chaim Sheba Medical Center
Sheba Medical Center
Not Provided
Principal Investigator: David Tanne, MD Sheba Medical Center
Sheba Medical Center
October 2009

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