Proprioceptive Stimulation With Manual Bilateral Rhythmic Exercise in Post-stroke Patients (NCT03155399) | Clinical Trial Compass
TerminatedNot Applicable
Proprioceptive Stimulation With Manual Bilateral Rhythmic Exercise in Post-stroke Patients
Stopped: PI transferred to another Institution
Italy34 participantsStarted 2013-07
Plain-language summary
The purpose of this study is to evaluate the effect of the repetitive proprioceptive bilateral stimulation for the early recovery of the voluntary muscle contraction in stroke patients.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. time since stroke up to 6 months,
. presence of the upper limb plegia (0 point according to the Medical Research Council scale),
. passive range of motion (ROM) completely free,
. absence of primary joint trauma of the wrist, elbow and shoulder,
Exclusion criteria
. increased muscle tone (score higher than 1 point in modified Ashworth scale),
. apraxia (De Renzi test \< 62 points),
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Medical Research Council scale (MRC)
Timeframe: Change from baseline of the MRC scale at the end of PBT (three weeks thereafter)
2
Dynamometer
Timeframe: Change from baseline of dynamometer at the end of PBT (three weeks thereafter)
. cognitive impairments (Mini Mental State Examination test \< 24 points) ,
. severe sensitivity disorders ( \< 1 point in items shoulder, elbow, wrist and thumb at the proprioceptive sensitivity section of the Fugl-Meyer scale),
. stroke lesion located in the cerebellum (clinical notes).