Integrative Yoga Therapy for Patients With Chronic Pain and Psychological Distress
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 72
- 试验地点
- 1
- 主要终点
- Symptoms of depression and anxiety
研究概览
简要总结
This study will be a randomized wait list controlled trial studying the efficacy of an Integrative Yoga Therapy for patients with chronic pain and psychological distress. Individualised yoga program will consist of a 8-week guided self-help program.
This study will primarily investigate whether an individually tailored yoga can be beneficial for patients suffering from chronic pain reducing pain, anxiety depression, while improving overall quality of life.
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
- Single (Outcomes Assessor)
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
- •Experienced pain for > 3 months
- •Experiences at least one type of psychological distress such as: depression, anxiety, insomnia or stress
- •Willing to provide informed consent
排除标准
- •Severe medical or psychiatric conditions
- •Alcohol or substance abuse
- •Active suicidality
- •Terminal illness
结局指标
主要结局
Symptoms of depression and anxiety
时间窗: From baseline to 8-week post intervention
Hospital Anxiety Depression Scale with 14 item. Each item on the questionnaire is scored from 0-3 where higher score represents increased anxiety and depression levels
Pain Disability
时间窗: From baseline to 8-week post intervention
Change in pain disability using Pain Disability Index (PDI) with 7 item.Each item scores on 0-10 numeric rating scale in which 0 means no disability and 10 is maximum disability
Pain Severity: Visual Analogue Scale
时间窗: From baseline to 8-week post intervention
Visual Analogue Scale ranging between 0-10 where 0 is no pain at all and 10 is worst pain
次要结局
- Self Efficacy: Pain Self-Efficacy Questionnaire (PSEQ)- 2 item scale(From baseline to 8-week post intervention)
- Insomnia symptoms(From baseline to 8-week post intervention)
- Mental well-being(From baseline to 8-week post intervention)