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

NCT ID: NCT05777421

Last Updated: 2023-03-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-01-01

Study Completion Date

2023-07-01

Brief Summary

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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.

Detailed Description

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Conditions

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Knee Osteoarthristis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

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.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Conventional Physical Therapy Regime for Knee Osteoarthrithis

Pt will receive conventional therapy targeting stretching and stretching of knee musculature in combination with electrotherapy for pain modulation.

Frequency : 2-3 times for a duration of 6 weeks Pt will be guided home plan based exercises.

Group Type ACTIVE_COMPARATOR

Conventional Physical Therapy for Knee Osteoarthriths

Intervention Type PROCEDURE

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

Virtual reality Based Therapeutic Exercise Regimes

VR-based therapeutic exercise regimes utilizing Xbox, that focus on different activities like Partial squatting, lunges, side lunge, calf raises, and hamstring curls.

Gaming exercises begin will an easy warm up round and get challenging with different rounds of each game as the patient progresses to week 6.

Frequency: 2-3 times for a duration for 6 weeks Pt will be guided home plan based exercises

Group Type EXPERIMENTAL

Virtual Reality-Based Therapeutic Exercise regimes

Intervention Type PROCEDURE

* 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.

Interventions

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Conventional 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

Intervention Type PROCEDURE

Virtual 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.

Intervention Type PROCEDURE

Eligibility Criteria

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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
Minimum Eligible Age

45 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Foundation University Islamabad

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Foundation University College of Physical Therapy

Rawalpindi, Punjab Province, Pakistan

Site Status

Countries

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Pakistan

Other Identifiers

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FUI/CTR/2023/5

Identifier Type: -

Identifier Source: org_study_id

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