Virtual Reality-based Mindfulness Training for Mental Health After Stroke
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 48
- 试验地点
- 1
研究概览
简要总结
Background: anxiety has a high prevalence in stroke patients and can dampen recovery of motor and cognitive impairment. Psychotropic medication can induce cognitive side effects, while psychotherapy and mindfulness-based stress reduction programs can be difficult to implement and are demanding for patients.
Aim: to evaluate the effect of a virtual reality (VR)-based medical device (HypnoVR®) on anxiety and stress reduction in patients with chronic stroke. Other outcomes, including depression, neurological fatigue and quality of life will be assessed.
Methodology: a randomized controlled trial including patients who had an ischemic or hemorrhagic stroke (>6 months) and experience significant anxiety - Hospital Anxiety and Depression Scale (HADS) ≥ 8 for anxiety. Intervention includes 3 weekly HypnoVR® sessions for 3 weeks (total: 9), with clinical assessments at baseline, post-intervention (end of week 3) and at a 8-week follow-up. The sessions will be supervised by a research assistant and will take place in our outpatient clinic. Participants will be randomly assigned to either an immediate treatment group or a delayed treatment group (waiting list), the latter acting as both controls and active participants.
Potential significance: VR-based therapeutic interventions are emerging as promising solutions to improve mental health but require solid scientific studies to assess their efficacy. This study provides a safe, non-invasive intervention for all included participants and could unveil its potential as an adjunctive therapy for mental health issues after stroke.
详细描述
Research aim: to assess the effectiveness of VR-based mindfulness training in outpatient stroke participants with mild-to-severe anxiety (HAD-anxiety ≥8). Secondary outcomes include depression, neurological fatigue, quality of life and sleep quality.
Methodology: randomized controlled trial of VR-based therapeutic intervention for patients with chronic (≥6 months) stroke and mild-to-severe anxiety (HAD-anxiety ≥8). The active group will benefit from 3 weekly HypnoVR® sessions for 3 weeks. This device is a head-mounted display providing medical hypnosis sessions with personalized visual (landscapes) and musical environments. Participants will be taken care of by a research assistant in our outpatient clinic and will experience 10- to 20-minute sessions. Clinical assessments include HADS for anxiety and depression, Multidimensional Fatigue Inventory Scale (MFIS), quality of life (SF-36) and sleep quality (Pittsburgh Sleep Quality Index). They will be measured at baseline (T0), post-intervention (T1, end of week 3) and at a 8-week follow-up (T2). A control group includes participants initially on a waiting list for 8 weeks (with T0-T1-T2 assessment) who will then benefit from the same active intervention (3 weekly HypnoVR® sessions for 3 weeks) with subsequent clinical reassessment (before starting the intervention (week 9, T0'), post-intervention (T1', end of week 11) and at a 16-week follow-up (T2').
Inclusion Criteria:
- Patient who had an ischemic or hemorrhagic stroke at least 6 months before inclusion
- aged ≥18 years
- HAD-anxiety scale score ≥8
- able to come to the clinic for study
- able to participate to sessions
Exclusion Criteria:
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Sequential
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Ischemic or hemorrhagic stroke >6 months before inclusion
- •Anxiety-HAD score at inclusion >= 8
排除标准
- •Blindness
- •Photo-sensitive epilepsy
- •unstable psychiatric condition
研究者
Nicolas Nicastro
PD Dr
University Hospital, Geneva