NCT06696469Recruiting
Feasibility and Reliability of Using BeCureTM Virtual Reality in Patients With Stroke
Feasibility and Reliability of Using BeCureTM Virtual Reality in the Evaluation of Upper Extremity Motor Functions in Patients With Stroke
Source: ClinicalTrials.gov · Last updated 22 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 34 (estimated)
- First submitted
- 14 Nov 2024
- Start date
- 22 Jun 2024
- Primary completion date
- 22 Jun 2026
- Lead sponsor
- Ankara University
- Diseases
- Stroke
- NCT number
- NCT06696469
What you commit to
- Study type: Observational
- Planned participants: 34
- From 22 Jun 2024 to the primary completion date, 22 Jun 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- History of seizures or epilepsy (except childhood febrile seizures),
- Severe aphasia, cognitive impairment (premorbid dementia) or psychiatric disorders,
- Patients with subarachnoid hemorrhage,
Other
- Arthritis or pain in the affected upper limb that limits repetitive exercise,
- Spasticity in the affected arm is 3 or more compared to MAS,
- Patients without sitting balance,
- Patients with posterior cerebral artery infarction,
- Patients with visual impairments that may affect the virtual reality application
Who the study is looking for
- Patients diagnosed with stroke according to the World Health Organization with an age range of 18-80 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 a spasticity level below 3 according to the Modified Ashworth Scale (MAS) in the affected upper extremity (MAS 1-5 rating system)
- Patients who agreed to participate in the study and signed the informed consent form
Age in the registry: 18 years to 80 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Ankara University School of Medicine Department of Physical Medicine and Rehabilitation Coordinator of this site? Confirm its status | Ankara | Turkey (Türkiye) | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.