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临床试验/CTRI/2025/08/092545
CTRI/2025/08/092545尚未招募不适用

EFFECT OF VIRTUAL REALITY WITH AND WITHOUT CONVENTIONAL PHYSIOTHERAPY IN THE MANAGEMENT OF MECHANICAL NECK PAIN IN DESK JOB WORKERS- A RANDOMIZED CONTROLLED TRIAL

Amulya H M1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年9月21日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
50
试验地点
1
主要终点
1. VAS

研究概览

简要总结

This randomized controlled trial aims to assess the effectiveness of virtual reality (VR) therapy with and without conventional physiotherapy in managing mechanical neck pain among desk job workers. Fifty participants aged 20 to 45 years who work on computers for at least 8 hours daily will be randomly assigned into two groups. Group A will receive only VR therapy using Oculus Go for 15 minutes twice weekly for 4 weeks, while Group B will receive the same VR therapy along with conventional physiotherapy exercises, including range of motion, strengthening, isometric, and stretching exercises. The study will evaluate outcomes such as pain intensity (VAS), cervical range of motion (using an inclinometer), and neck disability index (NDI) at three time points: baseline (week 0), post-intervention (week 4), and follow-up (week 8). The primary objective is to compare the effectiveness of VR therapy alone versus its combination with conventional physiotherapy, while the secondary objective is to examine the sustainability of VR therapy effects and determine its optimal dosage in a workplace setting. This study anticipates improved pain relief, function, patient engagement, and feasibility of VR as a workplace-based rehabilitation strategy.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Outcome Assessor Blinded

入排标准

年龄范围
20.00 Year(s) 至 45.00 Year(s)(—)
性别
All

入选标准

  • Desk job worker working on computers for more than or equal to 8 hours a day for more than or equal to 1 year.
  • Desk job worker with mechanical neck pain.
  • Participants who are willing to give written informed consent.

排除标准

  • Pregnant women
  • Psychiatric disorder
  • Uncooperative participants
  • Participants with any diagnosed pathology of neck
  • Participants with vertigo/ ear infections/ vision problems.
  • Participants with history of surgery around the neck or cervical spine.

结局指标

主要结局

1. VAS

时间窗: These outcome measures will be assessed at baseline, 4th week and 8th week of the intervention

2. ROM with inclinometer

时间窗: These outcome measures will be assessed at baseline, 4th week and 8th week of the intervention

3. NDI (neck disability index)

时间窗: These outcome measures will be assessed at baseline, 4th week and 8th week of the intervention

次要结局

未报告次要终点

研究者

发起方
Amulya H M
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Amulya H M

SDM COLLEGE OF PHYSIOTHERAPY

研究点 (1)

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