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Can a special exercise program help burn survivors walk again?

NCT ID NCT04368117

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether a structured physical therapy program (STAT) helps people with severe burns recover better than standard therapy. About 166 adults aged 18-65 with burns covering at least 15% of their body will take part at seven burn centers. The main goal is to see if they can walk farther in six minutes after treatment.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
physical therapy program
What this could lead to
If it works, this could lead to a standard therapy that helps burn survivors regain mobility and quality of life more effectively.
What could go wrong
This is a mid-stage trial with 166 participants, so results may not apply to everyone. The therapy is behavioral, so individual effort and adherence can vary.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 166 people

The number the study aims to enrol. It can still change while the study runs.

Started

Oct 2020

Expected to finish

Sep 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 65 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Age 18 to 65 years old 2. Total TBSA of 15% or greater with at least 10% TBSA of third-degree burn 3. Potential need for a skin graft procedure determined by the local burn surgeon 4. Survivable burn injury determined by the admitting local burn surgeon on admission Exclusion Criteria: 1. Non-survivable burn injury determined by the admitting local burn surgeon on admission 2. History of chronic renal failure requiring dialysis prior to injury 3. History of developmental delay or congenital cognitive disorders 4. Prior history of connective tissue disorders or autoimmune disease 5. Anoxic or traumatic brain injury 6. Prior history of cerebrovascular accident with residual mobility impairment 7. Neurologic injury or disease-causing mobility impairment 8. Prior history of leg amputation 9. Non-viable leg requiring amputation on admission 10. Anticipated inability to return for follow up testing after discharge 11. History of a New York Heart Association (NYHA) class IV congestive heart failure

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Health and Hospital Corporation dba Eskenazi Health

    Indianapolis, Indiana, 46202, United States

  • Johns Hopkins Bayview Medical Center

    Baltimore, Maryland, 21224, United States

  • Loyola University Medical Center

    Maywood, Illinois, 60153, United States

  • United States Army Institute of Surgical Research

    Fort Sam Houston, Texas, 78234, United States

  • University of California Davis Medical Center-Regional Burn Center

    Sacramento, California, 95817, United States

  • ValleyWise Health

    Phoenix, Arizona, 85008, United States

  • Wake Forest University Health Sciences

    Winston-Salem, North Carolina, 27157, United States

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