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Body Weight Supported Treadmill Training vs. Overground Walking Training in Persons With Chronic Stroke

Not Applicable
Completed
Conditions
Stroke
Difficulty Walking
Interventions
Behavioral: Overground walking training
Behavioral: Body weight supported treadmill training
Registration Number
NCT01180738
Lead Sponsor
Stephanie Miller
Brief Summary

The purpose of this study is to compare two different walking training programs for persons with chronic stroke.

Detailed Description

Body weight supported treadmill training (BWSTT) and overground walking training (OWT) are two interventions commonly applied for enhancing gait and balance in patients with chronic stroke. BWSTT and OWT are often used by clinicians separately or in tandem. While various aspects of the two interventions have been investigated in the past, limited research has been conducted to compare the effects of the two interventions in patients with chronic stroke.

Longer training durations may not always be feasible due to limited reimbursement options, lack of clinic accessibility, or transportation restrictions for patients with chronic deficits following stroke. A short burst of training consisting of a ''booster''-like protocol may provide a convenient option for some patients with chronic stroke to improve necessary functional skills in a short period of time.

The primary purpose of this pilot study is to compare walking speed immediately and 3-months after a short-burst of body-weight support treadmill training (BWSTT) or overground walking training (OWT) for adults with chronic stroke. Twenty participants with chronic stroke will be recruited and screened to determine eligibility for the study. Participants will be randomly assigned to either BWSTT or OWT for 30 minutes, 5 days per week for 2 weeks. Outcome measures will include assessments of gait speed, endurance, walking pattern, fear of falling, balance confidence, anxiety, and activity and participation in daily life. Outcomes will be tested prior to (pre-test) and immediately after (post-test) the assigned intervention and again 3-months after completing the intervention (retention).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Minimum of 6 months post-stroke
  • Single episode of stroke
  • Between the ages of 21-80
  • Able to walk with or without the use of an assistive device or orthoses
  • Able to ambulate at a self-selected gait speed < 0.8 m/s as determined by the 10-meter comfortable walk test
  • Medically stable with a physician release stating approval to enter an exercise program
  • Able to follow at least two-step verbal instructions
  • Available for the entire period of the study
  • Able to travel to and from research measurement and intervention sessions
Exclusion Criteria
  • Currently receiving physical therapy services
  • Co-morbidities or pre-existing cardiovascular conditions that would prohibit gait training and exercise
  • Pre-existing neurological or current musculoskeletal conditions that would limit gait ability separate from the effects of stroke
  • Complications from other health conditions that could influence walking
  • Currently known to be pregnant

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Overground walking trainingOverground walking training-
Body weight supported treadmill trainingBody weight supported treadmill training-
Primary Outcome Measures
NameTimeMethod
Gait speed: measured with the comfortable 10-meter walk testThe outcome measure will be assessed at pre-test (within 1-week before beginning the intervention), post-test (within 1-week after completing the 2-week intervention period) and at retention (3-months following completion of the intervention).
Secondary Outcome Measures
NameTimeMethod
Gait endurance: measured with the 6-minute walk test; Fear of falling: measured with the Fear of Falling questionnaire and Falls Efficacy Scale-InternationalThe outcome measures will be assessed at pre-test (within 1-week before beginning the intervention), post-test (within 1-week after completing the 2-week intervention period) and at retention (3-months following completion of the intervention).

Trial Locations

Locations (1)

University of Indianapolis, Krannert School of Physical Therapy

🇺🇸

Indianapolis, Indiana, United States

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