Virtual Reality in Hand Peripheral Nerve Injuries Effectiveness of Based Movement Therapy
NCT ID: NCT05898568
Last Updated: 2024-02-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
42 participants
INTERVENTIONAL
2023-04-01
2024-01-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effect of Virtual Reality Based Task Specific Exercises in Patients With Hand Flexor Tendon Injury
NCT06198582
Designing Virtual Reality-based Software for People With Multiple Sclerosis
NCT05420532
Additional Benefits of Virtual Reality Therapy for Individuals With Neck Pain
NCT06235515
Virtual Reality in Chronic Neck Pain
NCT06549166
Virtual Reality Approach in Multiple Sclerosis
NCT04212689
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
experimental: virtual reality
In 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.
virtual reality
In addition to the routine hand rehabilitation programs for 4 weeks, 5 days, 40 minutes a day, 20 sessions (4 weeks, 5 days a week, 20 minutes) virtual reality based movement therapy program will be applied.
control:routine treatment
20 sessions (4 weeks, 5 days a week, 60 minutes) routine hand rehabilitation program will be implemented.
routine treatment
20 sessions (4 weeks, 5 days a week, 60 minutes) routine hand rehabilitation program will be applied.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
virtual reality
In addition to the routine hand rehabilitation programs for 4 weeks, 5 days, 40 minutes a day, 20 sessions (4 weeks, 5 days a week, 20 minutes) virtual reality based movement therapy program will be applied.
routine treatment
20 sessions (4 weeks, 5 days a week, 60 minutes) routine hand rehabilitation program will be applied.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* clinical impression was made.
* out patient with median, ulnar, and radial nerve repair.
* completed the 6th postoperative week.
Exclusion Criteria
* With the musculoskeletal system, the additional passage, rheumatological, etc., where they are located.
those with the disease
\- Patients with multiple traumas
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Kocaeli University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Serkan Kablanoğlu
occupational therapist
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Kocaeli University
Kocaeli, Arızlı, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
E-66175679-514.13.02-960185
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.