Actively Recruiting

Phase Not Applicable
Age: 45Years - 80Years
All Genders
Healthy Volunteers
NCT07450274

Rehabilitation of Upper Limbs After Stroke

Led by University of Rzeszow · Updated on 2026-03-13

120

Participants Needed

1

Research Sites

30 weeks

Total Duration

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Sponsors

U

University of Rzeszow

Lead Sponsor

D

Donum Corde Rehabilitation Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Rehabilitation of Upper Limbs After Stroke

Who Can Participate

Age: 45Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Informed, voluntary consent of the patient
  • Age 45 to 80 years
  • Basic gripping ability
  • Degree of upper limb and hand paresis 4 to 5 on the Brunnstr�f6m scale
  • Degree of disability 3 on the Rankin scale
  • Spastic tension of upper limb, hand paresis not more than 3 on the modified Ashworth scale
  • Current health condition allowing participation in tests and exercises as confirmed by medical examination
Not Eligible

You will not qualify if you...

  • Lack of informed, voluntary consent of the patient
  • Second or subsequent stroke, hemorrhagic stroke, brainstem or cerebellum stroke
  • Disorders of higher mental functions limiting task comprehension and execution
  • Visual field disturbances
  • Mechanical or thermal injuries limiting hand grasping function
  • Concomitant neurological, rheumatological, or orthopedic diseases including permanent contractures affecting grasping or locomotion
  • Unstable medical condition
  • Failure to complete a 3-week rehabilitation stay

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Rzeszów

Rzeszów, Poland, 35-205

Actively Recruiting

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Research Team

J

Justyna K Leszczak, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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