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临床试验/NCT02330575
NCT02330575已完成不适用

Alberta Cancer Exercise Community-based Program: A Pilot Randomized Controlled Trial

University of Alberta4 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2015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
80
试验地点
4
主要终点
Feasibility: number of participants completing the objective outcome measurements for the study

研究概览

简要总结

The purpose of the study is to examine the benefit and specific outcomes of a community-based exercise program that is designed to address the needs of individuals who are receiving or recovering from cancer treatment.

Eighty cancer survivors from Edmonton and Calgary will take part in the 24-week long study. Survivors will be randomly assigned to one of two groups. The first group will take part in an 8-week supervised exercise program followed by 8 weeks of self-directed or home-based exercise (early exercise group). The other 40 participants will continue with their normal activities for 16 weeks (delayed exercise group). After the 16 week period, participants in the delayed exercise group will take part in the 8-week supervised exercise program.

Exercise sessions will take place at selected YMCAs in Edmonton and Calgary. Exercise sessions will be supervised by specially trained exercise specialists who have received special training in exercise and cancer.

Outcomes of the study will include feasibility, physical fitness measures, cancer-related symptoms and quality of life.

详细描述

Purpose: The primary purpose of this proposed study is to pilot test the planned Alberta Cancer Exercise (ACE) program evaluation components at the level of the individual cancer survivor. These components include program reach as well as effectiveness as determined by outcomes of physical fitness, symptoms, and quality of life. This proposed study will enable us to formalize an evaluation strategy to inform effectiveness and implementation of the ACE program.

Methods: A randomized controlled trial (RCT) design will be utilized to examine the short-term effectiveness of the proposed community-based cancer exercise program designed for cancer survivors. The study will take place at the Cross Cancer Institute/University of Alberta and Tom Baker Cancer Centre/ University of Calgary as well as in selected YMCA community fitness centres in Edmonton and Calgary. The exercise intervention will be delivered by specially trained exercise professionals who have completed the formal cancer exercise education course. Eighty participants will be randomized to early (intervention group) or delayed community-based exercise programming (standard care group). Participants randomized to the intervention group will undertake the ACE Program at a selected Edmonton and Calgary YMCA for an 8-week period. Following the 8-week supervised intervention period, participants will have the option to continue on a 'fee for service' basis or to continue with self-directed exercise at home. Participants allocated to the standard care group will receive standard advice and counseling on physical activity and will serve as the 'control group' for a 16-week period. The standard care group will be offered participation in the 8-week ACE program at the completion of the 16-week follow-up period.

Outcomes: The primary outcome is program feasibility: recruitment, completion and adherence rates. For the purposes of the proposed study and the length of follow-up of 24 weeks, the RE-AIM components of Reach, Effectiveness and Implementation at the level of the individual will be evaluated as potential outcome indicators for the ACE program. Outcomes will include measures of health-related physical fitness, cancer-related symptoms and quality of life.

Summary: ACE is an active living initiative, encouraging cancer survivors in Alberta to take a role in their own wellbeing by supporting participation in cancer-specific community-based exercise programs.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Within 18 months of a diagnosis of any type of cancer
  • Receiving or have received curative cancer treatment (e.g., surgery, chemotherapy, radiation therapy)
  • Cleared for unrestricted physical activity by their treating oncologist

排除标准

  • Presence of metastatic disease
  • Any uncontrolled or serious comorbid conditions that would preclude participation in exercise testing and training
  • Women who are pregnant

研究组 & 干预措施

Standard Care

Active Comparator

Participants in this group will receive standard education on the importance of physical activity in the recovery from cancer and how to become more active. Participants assigned to this group will have the option to participate in the exercise program after the 16-week follow-up assessment.

干预措施: Education (Behavioral)

Supervised Community-based Exercise

Experimental

Participants in this group will take part in an 8-week supervised exercise program at the YMCA. Following the 8-week intervention, participants will have the option to continue for an additional 8-weeks at the YMCA (fee for service) or follow an 8-week self-directed program.

干预措施: Exercise (Behavioral)

Supervised Community-based Exercise

Experimental

Participants in this group will take part in an 8-week supervised exercise program at the YMCA. Following the 8-week intervention, participants will have the option to continue for an additional 8-weeks at the YMCA (fee for service) or follow an 8-week self-directed program.

干预措施: Education (Behavioral)

结局指标

主要结局

Feasibility: number of participants completing the objective outcome measurements for the study

时间窗: 24 weeks

Proportion of subjects completing the physical fitness tests including aerobic capacity, musculoskeletal fitness and body composition measurements.

次要结局

  • Aerobic Capacity(8 weeks)
  • Health-related Quality of Life(8 weeks)
  • Symptom Assessment(8 weeks)
  • Adherence to exercise(24 weeks)
  • Recruitment rate(18 months)
  • Upper Extremity Muscular Strength (optional)(8 weeks)
  • Upper Extremity Grip Strength (optional)(8 weeks)
  • Lower Extremity Muscular Strength (optional)(8 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Margie McNeely

Associate Professor

University of Alberta

研究点 (4)

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