Actively Recruiting

Age: 18Years - 80Years
All Genders
Healthy Volunteers
NCT06696469

Feasibility and Reliability of Using BeCureTM Virtual Reality in Patients With Stroke

Led by Ankara University · Updated on 2024-11-22

34

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study is to demonstrate the feasibility and reliability of using virtual reality-based BeCureTM in the assessment of upper extremity motor functions in stroke patients.It is necessary to define the appropriate patient profile for the evaluation of upper extremity motor functions in stroke patients with virtual reality method. We aimed to examine the effects of demographic characteristics, accompanying cognitive disorders and upper extremity motor disorders that may affect the evaluation and response to treatment on virtual reality applications. Therefore, BeCure TM virtual reality system can be feasibly used in the evaluation and rehabilitation of stroke patients.

CONDITIONS

Official Title

Feasibility and Reliability of Using BeCureTM Virtual Reality in Patients With Stroke

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with stroke according to the World Health Organization aged 18 to 80 years
  • Patients with subacute to chronic stroke
  • Patients who can understand commands
  • Patients with sitting balance
  • Patients with a first stroke attack
  • Patients who have never received virtual reality therapy
  • Upper extremity Brunnstrom Stage III and above
  • Patients with spasticity level below 3 in the affected upper extremity according to the Modified Ashworth Scale
  • Patients who agreed to participate and signed the informed consent form
Not Eligible

You will not qualify if you...

  • History of seizures or epilepsy (except childhood febrile seizures)
  • Arthritis or pain in the affected upper limb that limits repetitive exercise
  • Severe aphasia, cognitive impairment (premorbid dementia), or psychiatric disorders
  • Spasticity level 3 or more in the affected arm according to the Modified Ashworth Scale
  • Patients without sitting balance
  • Patients with posterior cerebral artery infarction
  • Patients with subarachnoid hemorrhage
  • Patients with visual impairments that may affect the virtual reality application

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

Ankara University School of Medicine Department of Physical Medicine and Rehabilitation

Ankara, Turkey (Türkiye), 06620

Actively Recruiting

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Research Team

S

S. K. Professor

CONTACT

H

H. G. Professor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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