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NCT05727930Recruiting

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

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

Source: ClinicalTrials.gov · Last updated 27 Mar 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
100 (estimated)
First submitted
6 Feb 2023
Start date
11 Jan 2023
Primary completion date
15 Oct 2028
Lead sponsor
Indiana University
Diseases
Stroke
NCT number
NCT05727930

What you commit to

  • Study type: Interventional
  • Planned participants: 100
  • From 11 Jan 2023 to the primary completion date, 15 Oct 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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

Other

  • 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.

Who the study is looking for

  • 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

Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Rehabilitation Hospital of Indiana
Coordinator of this site? Confirm its status
IndianapolisUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.