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Robotic Walking Training Compared With Usual Care After Stroke

Compares robotic walking training with usual walking therapy in adults recovering from stroke.

Plain-language title generated from the registry record
Registry title: Early Robotic Gait Training After Stroke

Key facts

Where
Dallas, 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: NCT06430632, who can take part

Where in United States

  • Baylor Scott & White Institute for RehabilitationDallas, 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
Baylor Research Institute
Trial code
NCT06430632
Record updated
6 February 2026
Original description
The ERA Stroke project will compare the effects of robotic gait training (RGT) and usual care (UC) gait training in patients in the subacute phase of stroke recovery undergoing inpatient rehabilitation at the Baylor Scott \& White Institute for Rehabilitation (BSWIR).Read full original descriptionShow less

Early Robotic Gait Training After Stroke

The ERA Stroke project will compare the effects of robotic gait training (RGT) and usual care (UC) gait training in patients in the subacute phase of stroke recovery undergoing inpatient rehabilitation at the Baylor Scott \& White Institute for Rehabilitation (BSWIR).

Inclusion: 18-85 years of age; All types of stroke; Acute/subacute phase of recovery; Medically stable as deemed by a physician; Undergoing medical care and rehabilitation at BSWIR; All genders, races, and ethnicities; Meets Ekso robotic exoskeleton frame limitations; Continence or on a program for bladder and bowel management; Capacity and goal for walking recovery.

Exclusion: Concurrent neurological diagnoses (e.g., TBI, degenerative, CNS neoplasm); Profound cognitive impairment; Pregnancy.

ClinicalTrials.gov NCT06430632