Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
NCT07262528

fNIRS Neurofeedback for Post-stroke Hand Rehabilitation

Led by University of Rzeszow · Updated on 2026-04-21

30

Participants Needed

1

Research Sites

22 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Cardiovascular diseases are one of the main causes of disability. Among post-stroke individuals, 80% experience upper limb dysfunction, while only 5% to 20% of individuals regain full limb and hand function. The purpose of this study is to evaluate the effects of hand rehabilitation of post-stroke individuals using HEG Neurofeedback The study will include 30 participants in the early sub-acute phase post-stroke, who will be assigned to either the study group or the control group. Participants in the experimental group will follow a rehabilitation program extended with HEG Neurofeedback training, while participants in the control group will follow the standard rehabilitation program. The HEG Neurofeedback therapy equipment will be supplemented with new hand therapy software. During the exercises, patients will focus on a discussed and presented task, and once the expected level of concentration is reached, the software will trigger a virtual hand performing a finger flexion movement. Motor control of the hand will be assessed using the Fugl-Meyer Scale and Brunnström recovery stages.

CONDITIONS

Official Title

fNIRS Neurofeedback for Post-stroke Hand Rehabilitation

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals with hemiparesis after a first ischemic stroke
  • Stroke occurred no longer than 3 months ago (subacute phase)
  • Upper limb paresis rated between 2 and 4 by Brunnstrm recovery stages
  • Age between 18 and 70 years
  • Consent to participate in the study
Not Eligible

You will not qualify if you...

  • Unstable general health condition
  • Visual field disorders
  • Inability to sit independently
  • Cognitive impairment indicated by Mini-Mental State Examination score of 24 or less

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, 35-959

Actively Recruiting

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Research Team

A

Agnieszka Guzik

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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