Restraining the good arm may force the brain to rewire after stroke
NCT ID NCT05570461
First seen Sep 04, 2026 ยท Last updated Sep 04, 2026
Summary
This study tests a rehabilitation method called modified constraint-induced movement therapy (mCIMT) for people recovering from a stroke. Participants wear a mitten on their unaffected arm for several hours a day while practicing tasks with the affected arm. The goal is to see if this approach improves arm function better than traditional physical therapy alone.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Modified constraint-induced movement therapy (mCIMT), a rehabilitation approach that involves repetitive training of the affected arm while the unaffected arm is restrained with a mitten.
- What this could lead to
- If it works, this could offer a more effective rehabilitation method to help stroke survivors regain arm movement and independence.
- What could go wrong
- The trial is small and early, so results may not apply to all stroke patients. The therapy requires active participation and may be challenging or uncomfortable.
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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46 people
The number who actually took part.
- Started
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Aug 2023
- Finished
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Feb 2024
- 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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30 to 60 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\. Age 30 to 60 years * 2\. Both female \& male will be included. * 3\. Cognitive and lingual ability to communicate with the research staff. * 4\. A minimum of 10 degrees of active finger extension and 20 degrees of active wrist extension(16). * 5\. A history of a single stroke resulting in a hemiparesis Exclusion Criteria: * 1\. Recurrent stroke during the training period. * 2\. Neurological or orthopedic disorders prohibiting the use of the paretic arm. * 3\. Patients who doesn't show willingness to participate in the study.
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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
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LRH Peshawar
Peshawar, KPK, Pakistan
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?