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Efficacy of Virtual Reality Based Exercise Regimes on Kinesiophobia, Pain and Functional Disability in Patients With Knee Osteoarthritis

Efficacy of Virtual Reality Based Exercise Regimes on Kinesiophobia, Pain and Functional Disability in Patients With Knee Osteoarthritis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05777421
Enrollment
24
Registered
2023-03-21
Start date
2023-01-01
Completion date
2023-07-01
Last updated
2023-03-21

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

Conditions

Knee Osteoarthristis

Keywords

Range of Motion, Proprioception

Brief summary

Knee Osteoarthritis is one of the most prevalent degenerative conditions in Pakistan. Although a variety of Physical therapy treatments have been proven to be beneficial in patients with early stages of knee Osteoarthritis. However, a few secondary impairments like Kinesiophobia which is the fear of movement have been unaddressed. Usually after conventional physical therapy, patients find immediate or short-term relief and that leads to cessation of follow up sessions. In situations like these, kinesiophobia is the greatest threat to mobility and can eventually effect quality of life by decreasing functional disability.

Interventions

PROCEDUREConventional Physical Therapy for Knee Osteoarthriths

Participants of Group A will receive the conventional physical therapy for Knee Osteoarthistis for a duration of 6 weeks atleast 2 times a week

PROCEDUREVirtual Reality-Based Therapeutic Exercise regimes

* Participants of Group B will receive Virtual Reality Based therapeutic exercises on the Xbox. The difficulty level of the games will progess each week. The duration of training will also also progress at treatment week progresses. * Frequency: 2-3 times a week for 6 weeks. Minimum 12 sessions in total.

Sponsors

Foundation University Islamabad
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

This is a randomized controlled trial having two groups. One group will receive conventional physical therapy along with Natural apophyseal glides and the second will receive Natural Apophyseal Glides in addition to cranial base release with conventional physical therapy. Both groups will be recruited concurrently.

Eligibility

Sex/Gender
ALL
Age
45 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients with unilateral knee OA involving mediolateral compartment * Knee OA grade 2 * Aged 40-65 years * Both Male and Female * NPRS value greater than

Exclusion criteria

* Patients with history of * History of systemic disorder (e.g., rheumatoid arthritis, ankylosing spondylitis). * History of malignancy. * History of trauma. * Previous knee surgery. * Congenital musculoskeletal deformity (e.g., scoliosis, kyphosis). * Patients with history of fracture * Patients with history of Chondropatella Malacia

Design outcomes

Primary

MeasureTime frameDescription
Kinesiophobia6 weeksKinesiophobia will be measured using the Tampa Scale of Kinesiophobia
Pain intensity6 weeksWill be Measured using the Numeric Pain rating scale
Functional Disability6 weeksWill be measured using WOMAC Osteoarthritis Index

Countries

Pakistan

Outcome results

None listed

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