跳至主要内容
临床试验/NCT06990646
NCT06990646尚未招募不适用

VR-ACT After Stroke: a Feasibility RCT of a Virtual Reality Delivery of ACT for Pain Management and Mental Health in Patients With Chronic Post-Stroke Pain

University of Coimbra0 个研究点目标入组 30 人开始时间: 2025年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
30
主要终点
Pain intensity

研究概览

简要总结

This exploratory project aims to develop and pilot test, in a parallel group randomized controlled trial (RCT) design, the feasibility, acceptability, and preliminary efficacy of a self-management virtual reality (VR) 8-week program for pain management and mental health in patients with chronic post-stroke pain (CPSP), in two assessment moments (pre- to post-intervention).

详细描述

This project has three objectives: O1) to develop and test the feasibility and acceptability of a 8-week VR ACT program (VR-ACT) in a sample of CPSP patients; O2) to pilot test the efficacy of VR-ACT in improving pain, mental health, and adaptive psychological processes and skills, and in reducing the functional connectivity of the Triple Network (DMN, SN, and FPN); O3) To examine the cost-effectiveness of the VR-ACT. The current project will conduct a parallel group design Randomized Controlled Trial (RCT) and will follow a multi-method approach (qualitative and quantitative assessment).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •medical diagnosis of CPSP;
  • •age between 18 and 80;
  • •implicit de facto internet and computer literacy;
  • •willingness to comply with the study procedures.

排除标准

  • •currently with active malignancy; -
  • •severe cognitive impairment;
  • •currently undergoing any psychological intervention or VR-delivered pain management program;
  • •current severe psychiatric symptoms (i.e., psychosis; severe depression; non-suicidal self-injury; suicide attempt in the last month);
  • •language impairment with severe comprehension deficit;
  • •history of photosensitive epilepsy or previous experience of severe simulator sickness;
  • •other neurological conditions (e.g., dementia; Parkinson´s).

研究组 & 干预措施

VR-ACT

Experimental

8 modules of 3D immersive skills training (2 targeting awareness regulation skills; 3 promoting acceptance; 3 focused on behavioral change and commitment to valued action)

干预措施: VR-ACT (Behavioral)

Sham-VR

Sham Comparator

8 2D non-immersive distracting video animations delivered through a VR headset

干预措施: Sham-VR (Behavioral)

结局指标

主要结局

Pain intensity

时间窗: From enrollment to the end of treatment at 8 weeks

- The Numeric Rating Scale (NRS)

Pain Impact

时间窗: From enrollment to the end of treatment at 8 weeks

- Pain Disability Index (PDI)

Mental Health

时间窗: From enrollment to the end of treatment at 8 weeks

Mental Health: - Depression Anxiety and Stress Scale (DASS-21)

Psychological and Physical Quality of Life

时间窗: From enrollment to the end of treatment at 8 weeks

- World Health Organization Quality of Life - Bref (WHOQOL- Bref)

次要结局

  • Mindful Awareness(From enrollment to the end of treatment at 8 weeks)
  • Emotional Regulation(From enrollment to the end of treatment at 8 weeks)
  • Psychological Flexibility(From enrollment to the end of treatment at 8 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sérgio Andrade Carvalho

Doctor

University of Coimbra

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