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Operant Conditioning for Stroke Rehabilitation
Study Summary
This trial will test if muscles represented in the primary motor cortex can be trained to improve movement after stroke.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- I expect my current medication to stay the same for the next 3 months.You have a cochlear implant.I have a history of a neurological disease.I have moderate-to-severe physical impairments.You have a device like a pacemaker or metal in your body.I haven't had botulinum toxin injections in my arm for the last 3 months.You have a history of hearing or balance problems.My muscle stiffness is not severe.You have any kind of metal in your brain or skull, except for titanium. This includes things like metal fragments, clips, or splinters.I have had a seizure or convulsion in the past.I can undergo TMS and have a detectable muscle response in my more affected arm.I or my family members have a history of epilepsy.I am a stroke survivor with weakness on one side of my body.My wrist is weak; I can barely move it against gravity.You have a loss of feeling or sensation in your upper limbs.I am currently on medication for a mental health condition.I have a history of vertigo.I had a stroke in the middle part of my brain.My neurological condition has been stable for over 6 months.I have no known brain or nerve injuries.I have a bone or joint problem in my arms.I am between 40 and 75 years old.You had a negative response to TMS in the past.I have a history of a neurological condition.You have spinal or ventricular implants.I am between 40 and 75 years old.My mental ability is clear enough to understand and follow the study's requirements.I am unable to give consent by myself.You have a medical device implanted in your brain or neck to stimulate nerves.You have had a negative reaction to TMS treatment in the past.
- Group 1: ECR MEP conditioning - Stroke
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Are any neoteric participants being accepted into this research endeavor?
"According to the data available on clinicaltrials.gov, this medical trial is still open for participant recruitment and was initially posted on January 13th 2022 before receiving its last edit on May 12th of the same year."
How many participants are currently being considered for this clinical experiment?
"Affirmative. Data hosted on clinicaltrials.gov demonstrates that this trial, which was first published on January 13th 2022, is actively seeking participants. About 20 people are required to be enlisted from a single site."
What population is eligible to be part of this clinical research?
"This medical trial has allocated 20 vacancies for participants aged 40 to 75 who have had a stroke. Applicants need to be free of any neurological impairment, and must identify as either male or female."
Does the criteria for this research endeavor extend to those over sixty years of age?
"Participants in this clinical study must be aged 40 or older, but not exceeding 75 years of age."
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