Optimal Dosing of High-Intensity Locomotor Training for Step Attainment and Locomotor Outcomes in Stroke Patients Undergoing Acute Inpatient Rehabilitation

ConditionStroke
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-95
SponsorNYU Langone Health

About this trial

The purpose of this study is to elucidate optimal dosing for High Intensity Gait Training (HIGT) to reduce locomotor disability for those undergoing inpatient rehabilitation (IR) in the subacute phase of stroke recovery.

This is a randomized controlled trial conducted at a single IR facility. Investigators will randomize patients to receive one of two distinct HIGT interventions or a high step count intervention during standard care.

Eligibility criteria

Qualifiers

None

Disqualifiers

Weightbearing restrictions, uncontrolled cardiopulmonary, metabolic, infectious, or psychiatric disorders, which would preclude aerobic locomotor training

Estimated length of stay of less than 14 days

Non-ambulatory status prior to admission (unable to walk >50 meters)

Pregnant

Trial design

Treatments tested in this trial

  • Moderate-Intensity Locomotor Training Program
  • High-Intensity Locomotor Training Program
  • High-Step Count Locomotor Training Program

Treatment groups

20 Participants
are divided into 3 treatment groups

Sponsors and collaborators

NYU Langone Health

Lead sponsor

National Institutes of Health (NIH)

Collaborator