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RecruitingNCT07333079

Rehabilitation With Biofeedback for People After Stroke

Evaluation of the Effectiveness of Biofeedback Rehabilitation in People After Stroke

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
University of Rzeszow · Academic / Other
Sex
All
Age
45 Years – 80 Years
Healthy volunteers
Accepted

Summary

The aim of the research will be to evaluate rehabilitation using the biofeedback method in people after stroke.

Detailed description

Study participants will be randomly assigned to a study group and a control group. * Study group I - will complete a conventional rehabilitation program supplemented with biofeedback exercises using the Biometrics E-link device * Study group II - will complete a conventional rehabilitation program supplemented with biofeedback exercises using the Stella Bio device * Control group - will complete a standard spa rehabilitation program without biofeedback exercises. The study participants will be patients admitted to the Spa and Rehabilitation Hospital in Iwonicz-Zdrój, Poland, after a late-stage stroke. Patients will undergo continuous inpatient rehabilitation (3 weeks). The first examination will be conducted on the day of hospital admission, the second on the day of discharge, and the third (follow-up) 3 months after hospital discharge, during a follow-up visit. Prior to the study, a socio-demographic questionnaire will be administered, including questions about education, marital status, and place of residence. Measurements will be performed three times for all participants: * hand muscle strength assessment * calculated body mass index (BMI) * proprioceptive testing (mirror test, Thumb Location Test) * rehabilitation outcome assessment * functional capacity - Barthel Index, ADL * Ashworth muscle tone (spasticity) * hand dexterity using the Box and Blocks test * hand grip function according to the Frenchay scale * motor function of the hand and upper limb according to the Fugl-Meyer Motor Assessment Scale for Upper Extremity

Conditions

Interventions

TypeNameDescription
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).

Timeline

Start date
2026-01-19
Primary completion
2026-08-30
Completion
2026-09-30
First posted
2026-01-12
Last updated
2026-02-25

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT07333079. Inclusion in this directory is not an endorsement.