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Evaluation of the Effects of Upper Limb Rehabilitation Using the Pablo Tyromotion Device in People After Stroke
The aim of the research will be to evaluate the effects of upper limb rehabilitation using modern Pablo Tyromotion technologies in people after stroke in the late period.
Prior to the study, an assessment of the reliability, reproducibility and validity of the devices among stroke individuals will be carried out. The research will be conducted among people who have suffered a stroke in the late period. The subjects will be allocated, by random selection, to two groups: The study group will complete a conventional rehabilitation program supplemented with biofeedback exercises using the Pablo Tyromotion device. The control group will participate in conventional rehabilitation without biofeedback exercises. Patients will undergo ongoing rehabilitation at the Donum Corde Rehabilitation and Medical Care Center (four weeks). The first examination will be performed on the day of admission, the second on the day of discharge, and the third (control) one month after discharge, during a follow-up visit. Measurements will be performed three times for all participants: * assessment of hand and finger muscle strength * 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
Age
45 - 80 years
Sex
ALL
Healthy Volunteers
Yes
University of Rzeszów
Rzeszów, Poland
Start Date
March 2, 2026
Primary Completion Date
August 31, 2026
Completion Date
September 30, 2026
Last Updated
March 13, 2026
120
ESTIMATED participants
Rehabilitation program using upper limb function training with the Pablo Tyromotion device and conventional physiotherapy.
OTHER
Lead Sponsor
University of Rzeszow
Collaborators
NCT07371455
NCT05093673
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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View ClinicalTrials.gov Terms and ConditionsNCT06258538