We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov Menu

Structural Neuroplasticity Associated With Aerobic Treadmill Training in Geriatric Chronic Stroke Survivors

This study has been completed.
ClinicalTrials.gov Identifier:
First Posted: February 13, 2008
Last Update Posted: May 28, 2015
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.
Robert Bosch Medical Center
Max-Planck-Institute Tuebingen
Information provided by (Responsible Party):
Andreas R Luft, University Hospital Tuebingen

Aerobic treadmill exercise has been shown to improve walking, cardiovascular fitness and thereby risk factor profiles in chronic stroke patients (Macko et al., Stroke 2005). The proposed project is a randomized controlled trial in geriatric stroke patients with chronic disabilities to investigate potential mechanisms of treadmill therapy. The hypothesis is tested that 3-months of aerobic treadmill exercise induces structural brain plasticity and reorganization. The outcome measures are walking ability, gait pattern, cardiovascular fitness and brain morphology. This study will elucidate fundamental mechanisms of brain adaptations linked to task-repetitive aerobic lower extremity exercise. These mechanisms will not only lead to a better understanding but may also help to identify predictors of treatment response.

40 patients aged over 60 years with lower extremity paresis after a first-ever clinical stroke longer than 6 months prior to study inclusion will be recruited from: 1) The Geriatric Rehabilitation Clinic at the Robert-Bosch Hospital in Stuttgart 2) the Dept of Neurology, University Hospital in Tübingen. Subjects will be randomized to 3 months progressive graded aerobic treadmill exercise training (TAEX; 3 times/week, duration 10-45 min) or an attention control group (CON). Because we expect that localization and size of stroke affect therapy outcomes, stratified randomization will be used to balance entry into groups.

We hypothesize that 3 months of treadmill gait training but not conventional care leads to improvements of cardiovascular fitness and gait and to brain reorganization (structural plasticity) in regions in which functional adaptations have been demonstrated using fMRI in previous studies. The specific aims are:

  • To assess reorganization by comparing cortical thickness, cortical density and fiber tract morphology before (time point 0), and after therapy (3 months) using T1-weighted 3D-MPRAGE images, voxel based morphometry and diffusion tensor imaging.
  • To correlate brain reorganization with improvements in walking velocity, and analysis of gait patterns (parameters, swing time, stance time, gait symmetry).
  • To correlate brain reorganization with location and size of the index stroke lesion and of diffuse white matter damage (subcortical vascular encephalopathy). Lesion and white matter damage will be evaluated based on T2-weighted FLAIR sequences.

Condition Intervention
Stroke Hemiparesis Behavioral: treadmill exercise training

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Structural Neuroplasticity Associated With Aerobic Treadmill Training in Geriatric Chronic Stroke Survivors

Further study details as provided by Andreas R Luft, University Hospital Tuebingen:

Primary Outcome Measures:
  • aerobic capacity (peak VO2) [ Time Frame: Baseline (timepoint 0) and after training (3 months) ]
  • gait velocity [ Time Frame: Baseline (timepoint 0) and after training (3 months) ]

Secondary Outcome Measures:
  • cortical thickness (MRI) [ Time Frame: Baseline (timepoint 0) and after training (3 months) ]
  • grey matter density (VBM-MRI) [ Time Frame: Baseline (timepoint 0) and after training (3 months) ]
  • cerebrovascular reserve capacity (ASL-MRI) [ Time Frame: Baseline (timepoint 0) and after training (3 months) ]

Enrollment: 38
Study Start Date: January 2008
Study Completion Date: April 2010
Primary Completion Date: January 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: A
Treadmill training group (TAEX)
Behavioral: treadmill exercise training
3 months (3 times/week) progressive graded aerobic treadmill training with a duration of 10-45 min per training session
Active Comparator: B
Attention control group (CON)
Behavioral: treadmill exercise training
3 months (3 times/week) progressive graded aerobic treadmill training with a duration of 10-45 min per training session


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   60 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • women and men aged > 60 years
  • first ever ischemic stroke at least prior 6 months
  • all conventional inpatient and outpatient physical therapy completed
  • residual hemiparetic gait disturbance adequate language and neurocognitive function to participate in exercise training and testing

Exclusion Criteria:

  • already performing > 20 minutes aerobic exercise 3 X/ week
  • Alcohol consumption >2 oz liquor, or 2x 4oz glasses of wine, or 2x 12 oz cans of beer per day.
  • Cardiac history of

    1. unstable angina
    2. recent (< 3 months) myocardial infarction
    3. congestive heart failure (NYHA category II)
    4. hemodynamically significant valvular dysfunction.
  • Medical History:

    1. recent hospitalization (<3 months) for severe medical disease
    2. symptomatic peripheral arterial occlusive disease
    3. orthopedic or chronic pain conditions restricting exercise
    4. pulmonary or renal failure
    5. active cancer
    6. poorly controlled hypertension (>160/100) or diabetes mellitis (fasting glucose>180 mg/dl, HbA1C >10%)
  • Neurological history of

    1. dementia
    2. receptive or global aphasia that confounds testing and training, operationally defined as unable to follow 2 point commands
    3. cognitive deficits (other than dementia and aphasia, as above)

    (e) non-stroke neuromuscular disorder restricting exercise (eg Parkinson's Syndrome) (f) untreated major depression

  • exclusion criteria for MRI scanning (metal implants (e.g. pacemaker), claustrophobia, etc.)
  Contacts and Locations
No Contacts or Locations Provided
  More Information

Responsible Party: Andreas R Luft, Prof, University Hospital Tuebingen
ClinicalTrials.gov Identifier: NCT00614224     History of Changes
Other Study ID Numbers: BOSCH-TAEX-001
First Submitted: January 31, 2008
First Posted: February 13, 2008
Last Update Posted: May 28, 2015
Last Verified: January 2008

Additional relevant MeSH terms:
Cerebrovascular Disorders
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Vascular Diseases
Cardiovascular Diseases
Neurologic Manifestations
Signs and Symptoms