Effectiveness of virtual reality as an adjunct to conventional physiotherapy for cognitive impairments in patients undergoing chemotherapy: A randomized controlled trial.
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 26
- 试验地点
- 1
- 主要终点
- 1.Distress thermometer
研究概览
简要总结
This randomized controlled trial will evaluate the effectiveness of virtual reality (VR) as an adjunct to conventional physiotherapy in reducing chemotherapy-related cognitive impairment (CRCI) among cancer patients. CRCI, also known as “chemo brain,” affects memory, attention, and executive function, leading to reduced quality of life. A total of 26 participants aged 18–75 years with MMSE scores between 10–24 will be randomly assigned to receive either conventional physiotherapy alone or physiotherapy combined with VR-based training for two weeks. Outcome measures including Mini-Mental State Examination (MMSE), Functional Assessment of Cancer Therapy–Cognitive Function (FACT-COG v3), Distress Thermometer, and EORTC QLQ-C30 will be assessed at baseline and post-intervention. The study aims to generate evidence on whether VR combined with physiotherapy provides superior improvements in cognition, psychological well-being, and quality of life compared to physiotherapy alone.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 75.00 Year(s)(—)
- 性别
- All
入选标准
- •Patients diagnosed with cancer for the first time undergoing chemotherapy in the age group of 18-75 years of both genders, willing to participate.
- •Medically stable individuals.
- •Cognitive impairment score ranging from 10-24 according to MMSE.
排除标准
- •Patients receiving other forms of psychotherapy.
- •Patients having the following conditions- apraxia, neglect, aphasia or any visual impairments.
结局指标
主要结局
1.Distress thermometer
时间窗: Baseline and post intervention [ after 2 weeks]
2.FACT – Cog
时间窗: Baseline and post intervention [ after 2 weeks]
3.Mini-Mental State Examination
时间窗: Baseline and post intervention [ after 2 weeks]
4.EORTC QOQ C30
时间窗: Baseline and post intervention [ after 2 weeks]
次要结局
未报告次要终点
研究者
Dr Renuka Bhavsar
KLE Institute of Physiotherapy
