Can High-Repetition or High-Intensity training boost walking after stroke?
NCT ID NCT07725211
First seen Jul 24, 2026 · Last updated Jul 24, 2026
Summary
This trial tests whether adding either high-repetition task-oriented training or high-intensity gait training to standard neurodevelopmental therapy helps people with chronic stroke walk farther and move more easily. Forty-five participants who had a stroke at least six months ago will be randomly assigned to one of three groups for eight weeks of therapy. The study aims to see which approach, if any, leads to greater improvements in walking capacity and functional mobility.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- high-repetition task-oriented training and high-intensity gait training, added to neurodevelopmental treatment
- What this could lead to
- If one approach proves superior, it could point toward more effective rehabilitation strategies for regaining walking ability after stroke.
- What could go wrong
- This is a small, early-phase trial with only 45 participants, so results may not apply broadly. The improvements may be modest and not translate to real-world mobility.
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 45 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Aug 2026
An estimate. Start dates often move.
- Expected to finish
-
Dec 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 75 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 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: * Diagnosis of first-ever unilateral stroke (ischemic or hemorrhagic) confirmed by clinical and/or radiological findings * Time since stroke onset of at least 6 months (chronic phase) * Age between 18 and 75 years * Ability to walk at least 10 meters independently, with or without an assistive device * Functional Ambulation Category (FAC) score of 3 or higher * Sufficient cognitive ability to understand and follow instructions (Mini-Mental State Examination score ≥ 24) * Willingness to participate and provision of written informed consent Exclusion Criteria: * Recurrent stroke or bilateral hemispheric involvement * Unstable cardiovascular disease or other medical conditions contraindicating high-intensity exercise * Severe lower extremity spasticity interfering with gait training (Modified Ashworth Scale score \> 3) * Orthopedic, rheumatological, or other neurological conditions affecting gait * Severe visual or vestibular impairment * Severe aphasia or cognitive impairment preventing participation in training or assessments * Participation in another structured rehabilitation or exercise program during the study period * Botulinum toxin injection to the lower extremity within the last 6 months
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Chronic stroke are added.
By submitting, you agree to our Terms of use
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.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
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
-
Bingol State Hospital - City: Bingöl, Country: Türkiye (listede "Turkey" olarak geçebilir), Zip: 12000
Bingoel, Center, 12000, Turkey (Türkiye)
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?