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Clinical Trials/NCT06143176
NCT06143176
Not Yet Recruiting
N/A

Efficacy of Virtual Reality in Upper Extremity Rehabilitation for Stroke Patients

Bundang CHA Hospital0 sites10 target enrollmentNovember 27, 2023
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ConditionsStroke

Overview

Phase
N/A
Intervention
Not specified
Conditions
Stroke
Sponsor
Bundang CHA Hospital
Enrollment
10
Primary Endpoint
Fugl-Meyer Assessment of upper extremity
Status
Not Yet Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

To investigate the therapeutic effect of including virtual reality-based digital content in the upper limb motor function rehabilitation of stroke patients and to develop a treatment method to improve the upper limb motor function of stroke patients in the future.

Registry
clinicaltrials.gov
Start Date
November 27, 2023
End Date
November 27, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

MinYoung Kim, MD, PhD

Principle investigator

Bundang CHA Hospital

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • •Accompanying existing serious neurogenic disease
  • •Cases accompanied by existing serious psychiatric diseases such as major schizophrenia, bipolar disorder, dementia, etc.
  • •Cases where it is difficult to understand task performance due to severe cognitive decline (Korean Mini-Mental State Examination, K-MMSE 10 points or less)
  • •If there are difficulties in conducting research
  • •Other patients who are judged by the principal investigator to have difficulty participating in this study.

Outcomes

Primary Outcomes

Fugl-Meyer Assessment of upper extremity

Time Frame: baseline, 4 weeks after intervention

Fugl-Meyer assessment for motor function of upper extremity in score

Secondary Outcomes

  • Korean version of modified Barthel index(baseline, 4 weeks after intervention)
  • Korean version of mini mental state examination(baseline, 4 weeks after intervention)
  • Grip and pinch strength test(baseline, 4 weeks after intervention)
  • Nine-hole pegboard test(baseline, 4 weeks after intervention)
  • Motion analysis(baseline, 4 weeks after intervention)

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