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Virtual Reality in Hand Peripheral Nerve Injuries Effectiveness of Based Movement Therapy

Not Applicable
Completed
Conditions
Peripheral Nerve Injury, Virtual Reality, Rehabilitation
Interventions
Behavioral: routine treatment
Device: virtual reality
Registration Number
NCT05898568
Lead Sponsor
Kocaeli University
Brief Summary

The aim of this study is to investigate the effectiveness of virtual reality-based motion therapy in peripheral nerve injuries in the hand.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
42
Inclusion Criteria
  • ıt was operated in the early period with the diagnosis of peripheral nerve injury in the postoperative hand.
  • clinical impression was made.
  • out patient with median, ulnar, and radial nerve repair.
  • completed the 6th postoperative week.
Exclusion Criteria
  • Those who have communication problems and users
  • With the musculoskeletal system, the additional passage, rheumatological, etc., where they are located.

those with the disease

  • Patients with multiple traumas

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
control:routine treatmentroutine treatment20 sessions (4 weeks, 5 days a week, 60 minutes) routine hand rehabilitation program will be implemented.
experimental: virtual realityvirtual realityIn addition to routine hand care programs for 4 weeks, 5 days, 40 minutes a day, 20 sessions (4 weeks, 5 days, 20 minutes) virtual reality based movement therapy program will be applied.
Primary Outcome Measures
NameTimeMethod
Jebsen Taylor Hand Function Testfrom baseline to the end of the treatment (4 week)

Used to assess upper extremity functions. Activities are evaluated on a time basis.

Questionnaire Quick Disability of the Arm, Shoulder, and Hand (Quick DASH)from baseline to the end of the treatment (4 week)

activity participation level will be assessed by Q-DASH.Each question will be scored between 1-5 points (1: no difficulty, 2: mild difficulty, 3: medium difficulty, 4: extreme difficulty, 5: not at all). The total score will be recorded.

visual analog scale (VAS)from baseline to the end of the treatment (4 week)

marks the severity of pain between 0 and 10.

Sammes Weinstein Monofilament Test (SWMT)from baseline to the end of the treatment (4 week)

sensory threshold is used for assessment.sensed monofilament values will be collected and recorded. The highest total score will be considered as 15.

duruöz hand indexfrom baseline to the end of the treatment (4 week)

kitchen work, evaluates cleaning, workplace and other activities of daily living. The total score is between 0-90.

Jamar dynamometerfrom baseline to the end of the treatment (4 week)

Jamar dynamometer will be used for grip strength. 3 repetitive measurements will be made and the average will be recorded.(in kilograms)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Kocaeli University

🇹🇷

Kocaeli, Arızlı, Turkey

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