Functional Proprioceptive Stimulation of the Upper Limbs in Stroke Patients (NCT06143475) | Clinical Trial Compass
CompletedNot Applicable
Functional Proprioceptive Stimulation of the Upper Limbs in Stroke Patients
Russia60 participantsStarted 2021-02-20
Plain-language summary
Parallel-group, single-blinded controlled clinical trial. The study involved stroke patients (no more than 3 points on a scale Rankin) dived of the control group and experimental group. Control group received daily sessions of conventional physical therapy. In addition to the same conventional physical therapy treatment, the participants of the experimental group underwent repetitive upper limb Functional Proprioceptive Stimulations (FPS) sessions.
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:
* early recovery period after newly diagnosed cerebral stroke (from 2 weeks to six months post event)
* hospital stay 18-21 days
* 3 points on the Modified Rankin Scale
* muscle tone more than 1 point on the Ashworth scale
* informed consent signed
Exclusion Criteria:
* presence in the rehabilitation program of other robotic methods
* violation of skin integument
* floating thrombosis
* pronounced cognitive deficit
* epilepsy
* refusal to participate in the study
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
Muscle strength
Timeframe: Change from baseline at 3 weeks
2
Muscle tone
Timeframe: Change from baseline at 3 weeks
Trial details
NCT IDNCT06143475
SponsorFederal Center of Cerebrovascular Pathology and Stroke, Russian Federation Ministry of Health