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Effects of Regular Brisk Walking in Chronic Stroke Patients

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ClinicalTrials.gov Identifier: NCT01570920
Recruitment Status : Completed
First Posted : April 4, 2012
Last Update Posted : April 4, 2012
Sponsor:
Information provided by (Responsible Party):

Study Description
Brief Summary:
Chronic stroke patients (>6 months) fulfilling including criteria were trained during 3 months. The physical training program was based on walking.

Condition or disease Intervention/treatment
Stroke Behavioral: physical training

Detailed Description:
Participants had been evaluated 4 times during a long follow-up period of 7 months. Activity limitations were assessed at baseline (enrollment time point), 1 month, 4 months and 7 months later.

Study Design

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 34 participants
Intervention Model: Single Group Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Supportive Care
Official Title: Effects of Regular Brisk Walking in Chronic Stroke Patients
Study Start Date : September 2009
Primary Completion Date : December 2010
Study Completion Date : March 2011
Arms and Interventions

Arm Intervention/treatment
Experimental: walking
a cohort of stroke patients trained during 3 month, based on walking
Behavioral: physical training
walking many times a week


Outcome Measures

Primary Outcome Measures :
  1. ACTIVLIM-Stroke (Activity limitations measures) [ Time Frame: 7 months ]
    mainly self-reported outcomes measures


Secondary Outcome Measures :
  1. Stroke Impairment [ Time Frame: 7 months ]
    Stroke related impairment are assessed with specific outcomes measures (SIAS, BBS, ...).

  2. Walking ability [ Time Frame: 7 months ]
    Walking ability is assessed throuht walking speed and walking endurance


Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Stroke onset > or = 6 months
  • Able to walk without human assistance (may use walking aid)
  • Sign informed consent form
  • Approval from physician for participation in study
  • Live in Belgium or in Benin

Exclusion Criteria:

  • cardiac history of active unstable angina, recent (less than 3 months) myocardial infarction, or congestive heart failure
  • orthopedic, circulatory, or chronic pain conditions restricting exercise;
  • dementia;
  • severe receptive or global aphasia with inability to follow 2-step commands;
  • co-morbid non-stroke neurological disorder that impairs mobility (e.g. MS or Parkinson's);
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01570920


Locations
Belgium
Institut of Neuroscience (IoNS) / UCL, 5375
Brussels, Belgium, 1200
Sponsors and Collaborators
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Investigators
Principal Investigator: Jean-Louis Thonnard, PhD Université catholique de Louvain - Belgium
More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Cliniques universitaires Saint-Luc- Université Catholique de Louvain
ClinicalTrials.gov Identifier: NCT01570920     History of Changes
Other Study ID Numbers: 2008/04JUIL/193
First Posted: April 4, 2012    Key Record Dates
Last Update Posted: April 4, 2012
Last Verified: April 2012

Keywords provided by Cliniques universitaires Saint-Luc- Université Catholique de Louvain:
Activity limitations
restriction of participation
chronic stroke survival
physical activity
walking

Additional relevant MeSH terms:
Stroke
Cerebrovascular Disorders
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Vascular Diseases
Cardiovascular Diseases