跳至主要内容
临床试验/CTRI/2025/11/097550
CTRI/2025/11/097550已完成不适用

Effectiveness of virtual reality as an adjunct to conventional physiotherapy for cognitive impairments in patients undergoing chemotherapy: A randomized controlled trial.

Renuka Bhavsar1 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2025年11月25日最近更新:

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

发起方
Renuka Bhavsar
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Renuka Bhavsar

KLE Institute of Physiotherapy

研究点 (1)

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