Cognitive Behavioural Therapy-Informed Groups for Psychosis
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 主要终点
- Process of Recovery Questionnaire (QPR)
研究概览
简要总结
This is a feasibility study of cognitive behavioural therapy-informed groups for psychiatric inpatients with positive symptoms of psychosis.
详细描述
The majority of inpatients at Parkwood Institute Mental Health have symptoms of psychosis. In line with Health Quality Ontario standards for the treatment of psychosis, the investigators would like to implement and evaluate cognitive behavioural therapy for psychosis (CBTp) informed groups. The feasibility, acceptability, and preliminary efficacy of CBTp groups for inpatients will be examined. Pragmatically, the investigators propose to undergo training in CBTp, implement empirically-supported CBTp protocols developed for inpatients, track outcomes, and publish our findings. The investigators would also incorporate patient feedback to improve future iterations of the protocol. Such an undertaking would build research capacity in front line staff by encouraging engagement in CBTp group training, survey design, participant screening, data collection, analyses, and dissemination of findings.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Can read/write in English
- •Has positive symptoms of psychosis that are distressing to them
排除标准
- •Inability to tolerate group participation
研究组 & 干预措施
Treatment
Treatment group will receive cognitive behavioural therapy informed groups for psychosis.
干预措施: Cognitive Behavioural Therapy for Psychosis Groups (Behavioral)
Control
Control group will be put on a waitlist to receive cognitive behavioural therapy informed groups for psychosis.
结局指标
主要结局
Process of Recovery Questionnaire (QPR)
时间窗: Up to 2 months
The Process of Recovery Questionnaire is a 15 item questionnaire which was co-produced by people who experience psychosis and their accounts of recovery. The minimum value is 0, the maximum value is 60, and higher scores indicate a better outcome.
Clinical Outcomes in Routine Evaluation 10 (CORE-10)
时间窗: Up to 2 months
The Clinical Outcomes in Routine Evaluation 10 is a short 10 item easy-to-use assessment measure for common presentations of psychological distress, designed to be used for screening as well as over the course of treatment to track progress. The minimum value is 0, the maximum value is 40, and higher scores indicate a worse outcome.
次要结局
- The Positive and Negative Syndrome Scale (PANSS) - Positive Symptoms(Up to 2 months)
研究者
Serena Wong
Principal Investigator
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
