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Comparing How Often Walking Training Is Done After Stroke

Tests how often high-intensity walking training is done in adults with long-term stroke.

Plain-language title generated from the registry record
Registry title: High vs Low-frequency of High-intensity Training in Chronic Stroke

Key facts

Where
Indianapolis, United StatesSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 85 years old?

Source: NCT06612723, who can take part

Where in United States

  • Rehabilitation Hospital of IndianaIndianapolis, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Indiana University
Trial code
NCT06612723
Record updated
27 January 2026
Original description
The purpose of this pilot study is to investigate the potential role of training frequency on locomotor outcomes following high-intensity gait training and provision of a home walking program.Read full original descriptionShow less

High vs Low-frequency of High-intensity Training in Chronic Stroke

The purpose of this pilot study is to investigate the potential role of training frequency on locomotor outcomes following high-intensity gait training and provision of a home walking program.

Inclusion: Unilateral deficits following stroke \> 6 months prior; however individuals \> 4 months post-stroke are eligible for consenting, but final eligibility and potential enrollment will not occur until \> 6 months; Age 18-85; Weight \< 350 pounds; Able to follow 3-step commands; Able to ambulate with self-selected gait speeds between 0.10-1.0 m/s without physical assistance, but with below knee bracing and/or assistive device as needed; Lower extremity Fugl-Meyer \< 34; Medical clearance to participate.

Exclusion: Uncontrolled cardiopulmonary or metabolic disease that limits exercise participation, active heterotopic ossification, recurrent history of lower extremity fractures, previous orthopedic or other peripheral or central neurologic injury that may impair locomotor activities such that, in the judgement of the PI, could compromise the safety of the participant, limit the ability to complete the study, or compromise the objectives of the study; Currently participating in other physical therapy; Evidence of cerebellar ataxia; \>50 units of Botox in the lower extremity OR in the lower extremity, but above the knee if the participant wears an ankle-foot-orthosis (AFO) within the past three months.

ClinicalTrials.gov NCT06612723