RecruitingNot ApplicableNCT07333079
Rehabilitation With Biofeedback for People After Stroke
Evaluation of the Effectiveness of Biofeedback Rehabilitation in People After Stroke
Sponsor
University of Rzeszow
Enrollment
120 participants
Start Date
Jan 19, 2026
Study Type
INTERVENTIONAL
Conditions
Summary
The aim of the research will be to evaluate rehabilitation using the biofeedback method in people after stroke.
Eligibility
Min Age: 45 YearsMax Age: 80 Years
Inclusion Criteria6
- informed, voluntary consent of the patient
- age 45-80 years
- elementary (basic) gripping ability
- degree of paresis of the upper limb and hand 4 -5 on the Brunnström scale
- degree of disability on the Rankin scale 3
- spastic tension of the upper limb, paresis hand not more than 3 on the modified Ashworth scale - current health condition confirmed by a medical examination, allowing participation in tests and exercises
Exclusion Criteria8
- lack of informed, voluntary consent of the patient
- second or subsequent stroke, hemorrhagic stroke, stroke of the brainstem and cerebellum
- disorders of higher mental functions limiting comprehension and carrying out tasks during exercises
- visual field disturbances
- mechanical and thermal injuries that may limit the grasping function of the hand
- concomitant neurological, rheumatological and orthopedic diseases, including permanent - contractures that may affect the grasping ability and locomotion
- unstable medical condition
- failure to complete a 3-week rehabilitation stay
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Interventions
OTHERBiofeedback method using the Biometrics E-link (group I) and Stella Bio (group II) devices.
Patients in study groups I and II will also receive 30 minutes daily of hand biofeedback training using the Biometrics E-link device (group I) and hand biofeedback training using the Stella Bio device (group II).
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07333079
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