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Influence of Virtual Reality Games on Knee Proprioception After Anterior Cruciate Ligament Reconstruction (ACLR)

Influence of Virtual Reality Games on Knee Proprioception After Anterior Cruciate Ligament Reconstruction (ACLR)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03900351
Enrollment
30
Registered
2019-04-03
Start date
2019-04-07
Completion date
2019-06-13
Last updated
2019-06-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Balance; Distorted, Motor Activity, Proprioceptive Disorders

Brief summary

Influence of virtual reality games(Wii Fit) on knee proprioception after anterior cruciate ligament reconstruction (ACLR) will be measured in 30 postoperative patients. The age of participants will be ranged from 20 to 30 years old. Subjects will be randomly assigned to Group A is the study group and Group B is the control group.

Detailed description

Group A will receive the Wii fit protocol of virtual reality games, in addition to the regular exercise rehabilitation protocol, for 3 non-consecutive days per week, for 8 weeks , 40 minutes for each session. Group B will receive the regular exercise rehabilitation protocol only for 3 non-consecutive days per week for 8 weeks, 40 minutes for each session. 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).

Interventions

PROCEDUREWii 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 .

PROCEDURERegular exercise rehabilitation protocol

It will be according to the criterion of Adams et al. (2012).

Sponsors

University of Jazan
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

There are two group of subjects: 1. Group A (study group). 2. Group B:(Control group).

Eligibility

Sex/Gender
MALE
Age
20 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

1. patients who will be in the early postoperative phase (week 2 after surgery) 2. patients with BMI less than 25, and more than 20.

Exclusion criteria

1. Patients with injury or operation accompanied by the ACLR as meniscectomy. 2. Patients with any deformities affecting knee joint alignment as genu valgus, genu varus, or genu recurvatum.

Design outcomes

Primary

MeasureTime frameDescription
knee proprioception at 30 degrees3 minutesBiodex Isokinetic Dynamometer will be used to measure knee proprioception.
knee proprioception at 45 degrees3 minutesBiodex Isokinetic Dynamometer will be used to measure knee proprioception.
knee proprioception at 60 degrees3 minutesBiodex Isokinetic Dynamometer will be used to measure knee proprioception

Countries

Saudi Arabia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026