跳至主要内容
临床试验/CTRI/2026/01/101989
CTRI/2026/01/101989尚未招募1/2 期

Effect of virtual reality versus action observation therapy in post stroke survivors with depression- A randomized control trial

KAHER UNIVERSITY1 个研究点 分布在 1 个国家目标入组 74 人开始时间: 2026年2月15日最近更新:

试验速览

阶段
1/2 期
状态
尚未招募
发起方
入组人数
74
试验地点
1
主要终点
BDI-2

研究概览

简要总结

Title: Effect of virtual reality versus action observation therapy in post-stroke survivors with depression - A randomised control trial 

This study investigates the effect of virtual reality versus action observation therapy in post-stroke survivors with depression. Depression is a common psychological disorder that often accompanies post-stroke. Virtual reality and action observation therapy have shown successful improvement. Its immersive, multi-sensory approach can be beneficial in treating post-stroke depression.

This is an experimental interventional study involving 74 stroke survivors with at least one episode of stroke and a minimum time from the onset of stroke should be 3 months between the age group of 25-75 years conducted over 4 weeks. Participants will undergo a structured training protocol of duration of 3 sessions per week for 4 weeks, for 85 minutes.

The study aimed to evaluate the effectiveness of virtual reality and action observation therapy in reducing depression among stroke survivors.

研究设计

研究类型
Interventional
分配方式
Other
盲法
Participant Blinded

入排标准

年龄范围
25.00 Day(s) 至 75.00 Year(s)(—)
性别
All

入选标准

  • subjects with occurrence of first stroke, minimum time post onset of stroke should be 3 months
  • Diagnosed cases of Depression and evaluated by a Psychiatrist.
  • Participants with a score of 11 to 16 on Becks Depression Inventory II will be recruited.
  • Vividness of mental image scale will be used at screening tool to assess patients ability to perform the mental imagery efficiently.

排除标准

  • Subjects with previous history or cases with presence of any diagnosed Psychiatric illness.
  • Subjects not willing to participate in the study and difficulty in comprehension.
  • Participants with history of associated Neurological or Orthopedics conditions.
  • Subjects with visual impairments or vestibular dysfunctions and recent eye surgeries will not be included in the study.

结局指标

主要结局

BDI-2

时间窗: 10 minutes

次要结局

  • Stroke-specific quality of life(10 minutes)
  • Motor assessment scale(10 minutes)
  • Montreal Cognitive Assessment(10 minutes)

研究者

发起方
KAHER UNIVERSITY
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Sanjiv kumar

KLE institute of physiotherapy

研究点 (1)

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