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N/A N=34 Treatment

Long Term Split Belt Treadmill Training for Stroke Recovery

Stroke · Hemiparesis

Enrolled (actual)
34
Serious AEs
0.0%
Results posted
May 2018
Primary outcome: Primary: Change in Baseline Step Length Symmetry. That is, Whether the Steps With Right and Left Legs Are the Same Length. — 0.001; -0.078; -0.045; 0.144 ratio

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Split belt treadmill (Behavioral)
Age
Adult, Older Adult · 20+ yrs
Sex
All
Sponsor
Hugo W. Moser Research Institute at Kennedy Krieger, Inc.
Primary completion
Feb 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Baseline Step Length Symmetry. That is, Whether the Steps With Right and Left Legs Are the Same Length.
0.001; -0.078; -0.045; 0.144; -0.034; 0.010
SECONDARY
Change in Baseline Oxygen Intake
0.82; -.61; 0.65; 4.616; -2.272; 0.86
SECONDARY
Walking Speed
1.22; 0.5; 0.11; 0.12; 1.08; 1.17

Summary

The purpose of this study is to determine whether split belt or conventional treadmill training can be used to treat walking pattern deficits from stroke and to determine whether this improves gait asymmetry and metabolic efficiency.

Eligibility Criteria

Inclusion Criteria

  • stroke or hemiparesis (>6 months post stroke)
  • able to walk but has residual gait deficit (including those who walk with a cane or walker)
  • This is their first and only stroke
  • Able to walk for 5 minutes at their self-paced speed
  • Adults age 20-80

Exclusion Criteria

  • Cerebellar signs (e.g.ataxic hemiparesis)
  • Any neurologic condition other than stroke
  • Insulin dependent diabetes
  • Congestive heart failure
  • Peripheral artery disease with claudication
  • Pulmonary or renal failure
  • Unstable angina
  • Uncontrolled hypertension (>190/110 mmHg)
  • Dementia
  • Severe aphasia
  • Orthopedic or pain conditions that limit walking
  • Total joint replacement in the lower extremities
  • Pregnancy
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01646216). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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