Influence of Yoga on Cancer-Related Stress in Cancer Survivors
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 27
- 试验地点
- 2
- 主要终点
- Proportion of subjects who participate or show high adherence to the intervention
研究概览
简要总结
This clinical trial develops and test a yoga intervention in improving cancer-related stress in cancer survivors. The online hatha yoga intervention of breathing and movement incorporates both restorative poses, breathing techniques, guided meditation and may reduce stress levels and improve overall quality of health in cancer survivors.
详细描述
PRIMARY OBJECTIVE:
I. To develop and test the feasibility of a standardized 12-week online hatha yoga intervention (n=30) of breathing and movement incorporating both restorative poses, breathing techniques, guided meditation.
SECONDARY OBJECTIVES:
I. To evaluate the yoga intervention in relation to self-reported levels of stress and quality of life in cancer survivors (n=30).
II. Feasibility of collecting blood and saliva at baseline and post-intervention for stress biomarkers, including cortisol and norepinephrine.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 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
- •Age >= 18 years of age
- •Have been diagnosed with a cancer and have finished treatment
- •Have been cleared for physical activity by a physician or nurse practitioner (physician or nurse practitioner name and date clearance received)
- •Participant must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure
排除标准
- •Unwilling or unable to complete the assessment in English
- •Are pregnant or nursing
- •Are unwilling or unable to follow protocol requirements
- •Have skeletal instabilities and/or cardio-pulmonary comorbidities
- •Have any condition which in the investigator's opinion deems the subject an unsuitable candidate to participate in this study
结局指标
主要结局
Proportion of subjects who participate or show high adherence to the intervention
时间窗: Up to 12 weeks
Will be presented as observed proportion and 95% Clopper-Pearson confidence intervals (CIs).
次要结局
- Efficacy of the intervention in stress-reduction(Up to 3 months post intervention)
- Efficacy of the intervention in stress reduction(Up to 3 months post intervention)