Can a gentle robotic pull retrain balance after stroke?
NCT ID NCT07802470
First seen Sep 03, 2026 · Last updated Sep 04, 2026 · Updated 1 time
Summary
This trial tests whether treadmill training with a robotic cable that gently pulls walkers side-to-side can improve balance and daily walking in adults who had a stroke. Participants complete 20 high-intensity treadmill sessions, either with the robotic pulling forces or without them. Researchers measure walking balance, speed, and daily step counts before, during, and after training, plus at a 3-month follow-up.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- High-intensity treadmill gait training with a robotic cable device that gently pulls the participant side-to-side to challenge balance
- What this could lead to
- If it works, this training could become a standard rehab approach to help stroke survivors walk more steadily and take more steps in daily life.
- What could go wrong
- The trial is small (50 people) and early, so results may not apply to everyone. The robotic pulling forces might feel uncomfortable or not improve balance beyond standard training.
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
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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
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2031
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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. 18 to 80 years of age; 2. diagnosis of hemiparetic stroke; 3. more than 6 months post-stroke; 4. ability to ambulate over ground for 10 meters with no physical assistance, use of unilateral assistive devices, such as a single cane, and use of braces that do not cross the knee joint, such as an ankle-foot orthosis, are permitted; 5. passive range of motion of the legs within functional limits and not restricting the ability to engage in locomotor training and 6. medically stable with medical clearance from physician to participate. Exclusion Criteria: 1. cognitive impairment (score ≤22/30 on the Montreal Cognitive Assessment scale); 2. aphasia (score ≥71/100 on the Mississippi Aphasia Screening Test); 3. excessive spasticity in lower limbs (score \>3 on the Modified Ashworth Scale); 4. unable to tolerate 10-min. of standing; 5. enrollment in concurrent physical therapy; 6. use of orthotics crossing the knee joint; 7. known pregnancy; and 8. severe cardiovascular, musculoskeletal or other neurological conditions affecting gait and balance.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Northwestern University
Chicago, Illinois, 60611, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Effects of transcranial direct current stimulation and pelvic proprioceptive neuromuscular facilitation on trunk control, balance and functional mobility in stroke patients
- Correlation of visual and motor deficits in stroke patients
- Pilot study on the effects induced by an electromyographic-controlled functional electrical stimulator (FitFES) for upper limb rehabilitation in post-stroke patients
- Brazilian version of a behavior change intervention to support healthy lifestyle adoption after stroke - iVIDAVC: protocol for a pilot randomized study
- Determination of efficacy of sustained motor contraction generated using StimWave peripheral nerve stimulator
- Can a PET tracer reveal hidden brain inflammation?