Variable Intensive Early Walking Post-Stroke - 2 (VIEWS-2)

Description

The proposed research will evaluate the individual and combined effects of task-specificity and intensity of rehabilitation interventions on locomotor function, community mobility and quality of life in patients with subacute (1-6 months) post-stroke.

Conditions

Stroke

Study Overview

Study Details

Study overview

The proposed research will evaluate the individual and combined effects of task-specificity and intensity of rehabilitation interventions on locomotor function, community mobility and quality of life in patients with subacute (1-6 months) post-stroke.

Variable Intensive Early Walking Post-Stroke -2 (VIEWS-2)

Variable Intensive Early Walking Post-Stroke - 2 (VIEWS-2)

Condition
Stroke
Intervention / Treatment

-

Contacts and Locations

Indianapolis

Rehabilitation Hospital of Indiana, Indianapolis, Indiana, United States, 46254

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Sub-acute stroke (1-6 months)
  • * Hemiparesis (Fugl-Meyer \<34) without cerebellar deficits
  • * Ability to ambulate with or without physical assistance over 10 meters but \< 1.0 m/s and assistive devices and below-knee bracing is allowed.
  • * Ability to sit \> 30 seconds without upper-extremity support or physical assistance
  • * Ability to follow 3-step commands
  • * Provision of informed consent and medical clearance from a supervising physician or medical provider to participate
  • * Must have the ability to consent or have a legal health care power of attorney or legally authorized representative to consent for participation on their behalf
  • * Significant cardiovascular, metabolic, or respiratory disease that limits exercise participation (e.g. previous myocardial infarction \< 3 months prior, uncompensated congestive heart failure, resting blood pressure \> 210/110 mmHg, uncontrolled diabetes, end-stage renal disease, severe infectious or psychiatry disease, or advanced malignancy)
  • * If during the graded-treadmill exercise evaluation, the participant presents with absolute criteria for termination of exercise testing during initial testing (e.g. moderate to severe angina, ST elevation \> 1.0mm without preexisting Q wave secondary to prior MI, signs of poor perfusion, etc).
  • * Any orthopedic or neurological disorders that limited walking to \<50m prior to stroke onset.
  • * Cannot receive physical therapy once baseline testing begins
  • * If patients are prescribed botulinum toxin for their lower extremities will be excluded only if the dosage for any specific muscle is \>50 units in leg muscles above the knee. If doses are \> than 50 units in leg muscles below the knee, the participant will use an ankle-foot orthosis to minimze contributions of those mscles to locomotor function.

Ages Eligible for Study

18 Years to 85 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Indiana University,

George Hornby, PRINCIPAL_INVESTIGATOR, Indiana University

Study Record Dates

2028-12-31