ChiCTR2100050850进行中（未招募）不适用
Effects of a social participation-focused virtual reality intervention on the physical, psychological and social outcomes of community-dwelling stroke survivors with physical disabilities
General Research Fund, Research Grant Council1 个研究点 分布在 1 个国家目标入组 276 人开始时间: 2021年10月1日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 276
- 试验地点
- 1
- 主要终点
- Social participation
研究概览
简要总结
To develop and evaluate the effectiveness of a social participation-focused virtual reality (SP-VR) intervention on the physical, psychological, and social outcomes of community-dwelling stroke survivors with physical disabilities.
研究设计
- 研究类型
- 干预性研究
- 主要目的
- 随机平行对照
- 盲法
- None
入排标准
- 年龄范围
- 18 至 99（—）
- 性别
- All
入选标准
- •Participants will be recruited from the stroke units of three acute and one rehabilitation hospitals and three stroke nurss-led clinics in a single region. We will recruit 276 stroke survivor–caregiver dyads. The following inclusion criteria will be applied to the stroke survivors:
- •Aged >=18 years;
- •A diagnosis of ischaemic or haemorrhagic stroke resulting in physical disability;
- •Study entry within 6 months post-stroke;
- •The ability to remain in a sitting position with support;
- •A Montreal Cognitive Assessment score (HK-MOCA version) above the second percentile;
- •The absence of limb deformities and other neurological or musculoskeletal disorders;
- •Residence in the community. The study will include survivors of a first stroke and those with a history of stroke. Caregivers who provide most care to the survivor will also be included. Both members of the dyad must be able to communicate in Chinese.
排除标准
- •Both members of the dyad will be excluded if they have
- •A psychiatric condition (e.g. symptoms of delusion or hallucinations);
- •A history of vestibular deficits or severe visual impairments;
- •Any seizure activity during the previous 6 months;
- •Difficulty in following instructions.
研究组 & 干预措施
Two groups
Social-participation virtual reality
结局指标
主要结局
Social participation
时间窗: Data will be collected at baseline, and at immediately after and 3 months post-intervention.
次要结局
未报告次要终点
研究者
研究点 (1)
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