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临床试验/NCT02309112
NCT02309112已完成不适用

Yoga for Health-related Quality of Life in Adult Cancer: A Randomized Controlled Feasibility Trial

University of Oxford0 个研究点目标入组 15 人开始时间: 2014年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
15
主要终点
Feasibility of Patient Recruitment to Yoga Intervention

研究概览

简要总结

A feasibility study to determine the appropriateness of yoga intervention to improve health-related quality of life in adult cancer patients.

详细描述

A prospective, mixed methods feasibility trial allocated participants to receive one of three yoga interventions over a four-week study period. Data collection was completed through online survey of QOL-CA/CS and customized surveys.

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
None

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Male and female adult cancer patients 19 years of age or older
  • •Patients receiving or planning to receive conventional treatment that includes at least one of chemotherapy, radiotherapy, hormone therapy or active surveillance within 28 days
  • •Patients in any stage of cancer diagnoses of all tumour types and locations
  • •Participants with internet access and willingness to participate in online communication
  • •Participants with access to transportation and personal willingness to attend meetings in central Vancouver, Canada.
  • •Participants fluent in the English language

排除标准

  • •Patients with any physical limitation, risk of personal injury or under proscription of light to moderate physical activity
  • •Patients with pre or post surgical interventions were excluded due to potential physical limitations or safety concerns with wound healing
  • •Regular or experienced practitioners of yoga were excluded and defined as those patients reporting current or historical use of regular yoga (>2 session per month in past 12 months)
  • •Patients undergoing medical treatment for serious psychological disturbances that might have interfered with adherence to protocol and/or ability to provide informed consent were excluded (e.g. multiple personality disorders, severe depression, obsessive-compulsive disorder)

研究组 & 干预措施

Yoga Group A: Minimum Exposure

Experimental

The minimum-exposure yoga package, this intervention included 45-minutes of contact time with a trained yoga professional. In Week 1, this session included a 30-minute introductory session focussing on pranayama (breathing techniques), as well as a brief introduction to available community-based and online yoga to encourage a safe home-based practice (15-minutes). Financial subsidy, compensation or special promotion of any particular yoga was not provided. Participants were invited to stay for a social discussion following the yoga class.

干预措施: Yoga (Other)

Yoga Group B: Medium Exposure

Experimental

The medium-exposure yoga package, this intervention included the components of Group A, with an additional 30-minute orientation and safety training of how to practice yoga dhyana (meditation techniques) and asana (physical postures) in Week 1. Participants were then invited to stay and ask questions following the yoga class. A pre-paid online yoga membership to http://www.myyogaonline.com was offered for the duration of the study (Weeks 1 to 4). In addition to this, one 120-minute workshop to further develop yoga pranayama, dhyana and asana training was administered by an expert instructor during Week 2 or 3.

干预措施: Yoga (Other)

Yoga Group C: Maximum Exposure

Experimental

The maximum-dose yoga package, this intervention includes the components of Group A, with the same 30-minute orientation and safety training of how to practice yoga dhyana (meditation techniques) and asana (physical postures) in Week 1. Participants were invited to stay and ask questions following the yoga class. As in Group B, a pre-paid online yoga membership to http://www.myyogaonline.com was also provided for the duration of the study (Weeks 1 to 4). Participants were then invited to attend three 60-minute yoga group classes led by an expert yoga instructor per week (Weeks 1 to 4). These yoga sessions were held in a clinical setting in proximity to their treatment location and delivered at no cost to the patient.

干预措施: Yoga (Other)

结局指标

主要结局

Feasibility of Patient Recruitment to Yoga Intervention

时间窗: 10 weeks

Number of participants eligible for randomization to yoga intervention during cancer treatment

次要结局

  • Patient Adherence to Yoga Intervention(6 weeks)
  • Patient Adherence Rate to Yoga Intervention(6 weeks)

研究者

申办方类型
Other
责任方
Sponsor

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