A study on the effect of immersive virtual reality based exercises along with conventional exercises on quality of life in knee osteoarthritis patients

Addition of Immersive Virtual Reality mediated program with Conventional Physiotherapy on Quality of Life in Knee Osteoarthritis - A Randomized Controlled Trial. - nil

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/070120

Enrollment

Registered

2024-07-05

Start date

Unknown

Completion date

Unknown

Last updated

2024-07-22

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

Conditions

Health Condition 1: M179- Osteoarthritis of knee, unspecified

Interventions

Intervention1: Immersive Virtual Reality Group: immersive virtual reality group are provided with [Supervised VR Exercises+ Conventional Physiotherapy] that is with Immersive virtual reality exercis

Eligibility

Inclusion criteria

Inclusion criteria: Diagnosed with primary knee OA based on the American College of Rheumatology (ACR) clinical classification criteria, at least 3 of the following should be positive Age should be greater than 50 years old Morning stiffness should be less than 30 minutes Crepitus on knee motion Bony tenderness Bony enlargement No palpable warmth Having unilateral or bilateral grade 2 or 3 of knee OA according to the Kellgren and Lawrence radiological gradings a TSK-KA-11 score 23 or higher.

Exclusion criteria

Exclusion criteria: have cognitive impairment, have underwent a history of knee surgery, joint infection Rheumatoid arthritis of knee inflammatory arthritis any past six-month history of hip or knee replacement surgeries, intraarticular steroidal injections, arthroscopic surgeries. Persons who are all in need of external support for walking

Design outcomes

Primary

Measure	Time frame
quality of life by Knee Injury and Osteoarthritis Outcome Score (KOOS)Timepoint: 0 week of treatment,6th week of treatment,12th week of treatment,24th week of treatment.	—

Secondary

Measure	Time frame
fear of movement by Kinesiophobia by Tampa scale of kinesiophobia [Tampa scale of kinesiophobia Kannada version TSK-KA-11Timepoint: 0 week of treatment,6th week of treatment,12th week of treatment,24th week of treatment.;Functional Performance Test by 40Meter Fast paced Walk TestTimepoint: 0 week of treatment,6th week of treatment,12th week of treatment,24th week of treatment.;Knee Extensors Muscle Strength by Hand Held DynamometryTimepoint: 0 week of treatment,6th week of treatment,12th week of treatment,24th week of treatment.;Pain Pressure Threshold by AlgometryTimepoint: 0 week of treatment,6th week of treatment,12th week of treatment,24th week of treatment.;Pain Self-Efficacy QuestionnaireTimepoint: 0 week of treatment,6th week of treatment,12th week of treatment,24th week of treatment.	—

Measure

Time frame

fear of movement by Kinesiophobia by Tampa scale of kinesiophobia [Tampa scale of kinesiophobia Kannada version TSK-KA-11Timepoint: 0 week of treatment,6th week of treatment,12th week of treatment,24th week of treatment.;Functional Performance Test by 40Meter Fast paced Walk TestTimepoint: 0 week of treatment,6th week of treatment,12th week of treatment,24th week of treatment.;Knee Extensors Muscle Strength by Hand Held DynamometryTimepoint: 0 week of treatment,6th week of treatment,12th week of treatment,24th week of treatment.;Pain Pressure Threshold by AlgometryTimepoint: 0 week of treatment,6th week of treatment,12th week of treatment,24th week of treatment.;Pain Self-Efficacy QuestionnaireTimepoint: 0 week of treatment,6th week of treatment,12th week of treatment,24th week of treatment.

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Countries

India

Contacts

Public ContactR kamalakannan

Srinivas University, Mangalore, Karnataka

kamalakannan.pt@gmail.com9500931424

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026