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