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Comparison of virtual reality exercises and hands on therapy for neck pain neck function and fear of movement in young adults with recent neck pain

Comparing the Effects of Virtual Reality-Based Exergaming and Muscle Energy Technique on Pain, Functional Disability, and Kinesiophobia in Young Adults with Acute Neck Pain - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099477
Enrollment
114
Registered
2025-12-19
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecified

Interventions

Intervention1: Virtual reality group: Participants will receive a hot pack to the cervical region for 15 minutes followed by 15 to 20 minutes of VR based exergaming using a VR box with immersive apps.

Sponsors

Monika Hariramani
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants with acute nonspecific neck pain of 1 to 3 weeks duration and NPRS score greater than 3.

Exclusion criteria

Exclusion criteria: History of recent neck surgery or trauma, neurological deficits or cervical radiculopathy, radiating pain or vertigo, current use of muscle relaxants or NSAIDs, or any systemic condition affecting the cervical region.

Design outcomes

Primary

MeasureTime frame
The outcome measures in this study will include pain intensity, neck disability, and kinesiophobia. Pain intensity will be assessed using the Numerical Pain Rating Scale (NPRS). Neck disability will be evaluated using the Neck Disability Index (NDI), a validated questionnaire that measures the degree of functional limitation experienced due to neck pain in daily activities. To assess the psychological aspect of pain, particularly the fear of movement, kinesiophobia will be measured using the Tampa Scale for Kinesiophobia (TSK), which quantifies movement-related fear.Timepoint: Baseline Measurement (Day-0), Post intervention measurement (AFTER 2 WEEKS)

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactArvind Tomar

Mahatma Gandhi University of Medical Sciences and Technology

drarvindtomar@mgumst.org9784805133

Outcome results

None listed

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