Influence of Virtual Reality Games on Knee Proprioception After Anterior Cruciate Ligament Reconstruction (ACLR)
NCT ID: NCT03900351
Last Updated: 2019-06-14
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
30 participants
INTERVENTIONAL
2019-04-07
2019-06-13
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.
Virtual Reality Rehabilitation for Patients With Anterior Cruciate Ligament Reconstruction
NCT05080894
Effect Of Games Based Virtual Reality On Promoting Early Functional Recovery After Foot Tendon Repair
NCT07054814
VR-Based Preoperative Rehabilitation Program for Patients Undergoing Anterior Cruciate Ligament (ACL) Reconstruction
NCT06347523
The Effectiveness of Leap Motion-Based Virtual Reality in the Rehabilitation of Flexor Tendon Injuries of the Hand
NCT07201740
Proprioceptive Isokinetic Repositioning, Functional Testing, and a Self-reported Questionnaire Before and After Anterior Cruciate Ligament Reconstruction
NCT04058574
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
A Universal Weight and Height Scale: will be used to measure the patient's BMI.
Biodex Isokinetic Dynamometer: will be used to assess the knee proprioception of the affected operated leg at three target angles (30,45,and 60 degrees).
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
1. Group A (study group).
2. Group B:(Control group).
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Group A: Study group
They will receive the Wii fit protocol of virtual reality games for 40 minutes, 3 times per week, for 8 weeks, in addition to the regular exercise rehabilitation protocol according to the criterion of Adams et al. (2012).
Wii fit protocol of virtual reality games
the Wii fit session by standing on the Wii fit board with bare feet, hands on hips and both eyes open. Pretest on Wii fit was done to make the subject familiar with the board and tasks of weight shift .
Regular exercise rehabilitation protocol
It will be according to the criterion of Adams et al. (2012).
Group B: Control group
They will receive the regular exercise rehabilitation protocol only for 40 minutes, for 3 days per week, for 8 weeks.
Regular exercise rehabilitation protocol
It will be according to the criterion of Adams et al. (2012).
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Wii fit protocol of virtual reality games
the Wii fit session by standing on the Wii fit board with bare feet, hands on hips and both eyes open. Pretest on Wii fit was done to make the subject familiar with the board and tasks of weight shift .
Regular exercise rehabilitation protocol
It will be according to the criterion of Adams et al. (2012).
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. patients with BMI less than 25, and more than 20.
Exclusion Criteria
2. Patients with any deformities affecting knee joint alignment as genu valgus, genu varus, or genu recurvatum.
20 Years
30 Years
MALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Jazan
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Mohammed Moustafa
Principal invsetigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Jazan University
Jizan, Jazan Region, Saudi Arabia
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.
2387594650
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.