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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorAnkara University

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

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 in the affected arm is 3 or more compared to MAS,

Trial population

Post-stroke patients consecutively admitted to Ankara University Faculty of Medicine, Department of Physical Medicine and Rehabilitation will be included in the study.

Trial design

Design model

Case-control

Time perspective

Cross-sectional

Treatments tested in this trial

  • Feasibility and reliability of using BeCureTM Virtual Reality in the evaluation of upper extremity motor functions in stroke patients

    Diagnostic test

    The applicability and reliability of virtual reality systems are important factors to consider. Based on this, this study aimed to investigate the feasibility of using BeCureTM virtual reality in the evaluation of upper extremity functions after stroke.The feasibility of using BeCureTM virtual reality in stroke patients will be determined according to the System Usability Scale (SUS) score.The safety of the use of BeCureTM virtual reality in stroke patients will be assessed with a patient feedback questionnaire. The relationship between the use of BeCureTM virtual reality and cognitive functions in stroke patients will be determined by the Montreal Cognitive Assessment Scale and Mini Mental State Examination.It was 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.

Treatment groups

34 Participants
are divided into 1 treatment group
Group A: Patient group1 intervention

Trial outcomes

Primary outcomes

1

The feasibility of using BeCureTM virtual reality in stroke patients will be determined according to the System Usability Scale (SUS) score.

The System Usability Scale (SUS) is a simple, ten-item Likert scale of subjective evaluations of usability. It was developed in 1986 by John Brooke for usability evaluation. In short, it is a standardized questionnaire to measure users' satisfaction with a product or system. At the same time, a score between 0-100 can be obtained with SUS. When calculating the exact score, 1 is subtracted from the given value of items 1, 3, 5, 7 and 9 (odd numbered and positive opinion). The scores for items 2, 4, 6, 8 and 10 (items with negative opinions) are subtracted from 5. The SUS score can then be found by adding them all together and multiplying this sum by 2.5 to complete the 0-100 range. The minimum score is 0 points and the maximum score is 100 points. A higher score indicates better usability.

Time frame
Baseline and 7 days

Secondary outcomes

1

1- A patient feedback questionnaire on the safety of BeCureTM virtual reality use will be completed.

1. Patient feedback questionnaire will be completed for the reliability of BeCureTM virtual reality use in stroke patients. 2. The relationship between the use of BeCureTM virtual reality and cognitive functions in stroke patients will be determined by the Montreal Cognitive Assessment Scale and Mini Mental State Examination.

Time frame
Baseline and 7 days

Other outcomes

Sponsors and contacts

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