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临床试验/NCT04771975
NCT04771975已完成不适用

Connecting Breast Cancer Survivors for Exercise: A Randomized Controlled Trial Phase I and II

Jenna Smith2 个研究点 分布在 1 个国家目标入组 108 人开始时间: 2021年5月10日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
108
试验地点
2
主要终点
Phase 1 and Phase 2: Change in exercise volume

研究概览

简要总结

Phase 1: The purpose of this study is to examine interpersonal and individual effects of partnering BCS with a peer and a qualified exercise professional (QEP) on self-reported exercise volume (MVPA; primary outcome), and device-measured exercise volume (MVPA; Fitbit), social support, and HRQOL (secondary outcomes). Cost-effectiveness and intervention adherence will also be explored as tertiary outcomes. The effects of a peer and QEP-support intervention group, labelled MatchQEP, will be compared to a control group of BCS who are matched with a peer, but not a QEP, labelled Match.

Phase 2: The purpose of this study is to examine whether the addition of 8-weekly QEP-lead resistance training Zoom sessions with an exercise partner interacts with social support (i.e., tangible, informational, emotional) and how this interaction relates to overall exercise volume as an extension of Phase 1 (one year after phase 1 was completed). A secondary aim of Phase 2 is to examine the direct influence of resistance training on body image, self-efficacy, the physical self, and body functionality among the participants.

详细描述

The purpose of this project is to examine naturally occurring social support as related to daily exercise behavior. In our ecological momentary assessment (EMA) study, the function of social support (tangible, informational, emotional) was be explored as independent variables, and exercise dose (minutes, intensity) and type (aerobic, resistance training, flexibility) will be examined as dependent variables. The associations will be used to inform motivational and behaviour change messaging in ActiveMatch, a program developed and run by the PI of this study, Dr. Catherine Sabiston. It is generally hypothesized that the provision of social support will be associated with greater exercise behaviour. In phase 1 of Connect for exercise, the RCT portion of this study, the addition of qualified exercise professional (QEP) support will be evaluated compared to social support from a participant match (exercise partner) alone. In Phase 2 of the Connect for exercise trial (pre-post design with no control group), we will examine whether the addition of 8-weekly QEP-lead resistance training Zoom sessions with an exercise partner interacts with social support (i.e., tangible, informational, emotional) and how this interaction relates to overall exercise volume (completed one-year post phase 1 completion). A secondary aim of Phase 2 is to examine the direct influence of resistance training on body image, self-efficacy, the physical self, and body functionality among the participants. There is evidence that resistance training improves these outcomes in women (Santa Barbara et al., 2017), but the relationship is understudied in breast cancer survivors. Improvements in these outcomes have, in turn, been related to increases in PA and sustainable positive PA outcomes. Considering the decreases in body image and body functionality appreciation reported by BCS during and after treatment (Resaei et al., 2016), this relationship warrants further investigation.

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
Double (Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Breast cancer survivors
  • Stage 1-4 cancer
  • Aged >18 years
  • Have been cleared for exercise
  • Have consistent access to an Internet-connected device
  • Currently exercise ≤ 150 minutes per week.

排除标准

  • Report contraindications to exercise such as physical disability
  • Had recent or planned reconstructive surgery
  • Have no consistent access to an Internet-connected device
  • Are currently meeting exercise guidelines (performing > 150 minutes of moderate-to- vigorous exercise)
  • Have not been cleared to participate in exercise

结局指标

主要结局

Phase 1 and Phase 2: Change in exercise volume

时间窗: 26-weeks post baseline

The Godin Leisure Time Exercise Questionnaire will be used to measure exercise volume over 1 week. It is a self-report measure which asks respondents to give weekly frequencies and durations of strenuous, moderate, and mild aerobic activities and resistance training sessions. Together responses are summed to determine a total weekly leisure activity score. It is shown to be reliable and valid (r=.53) when classifying respondents into 'insufficiently active' and 'active' categories (Amireault \& Godin, 2015; Amireault et al., 2015; Amireault et al., 2015; Godin \& Shephard, 1985b). Respondents are classified as 'active' by exceeding a score of 24 on this scale (Amireault \& Godin, 2015; Amireault et al., 2015; Amireault et al., 2015).

次要结局

  • Phase 1 and Phase 2: Change in exercise volume(Baseline, 10-weeks post-baseline, 14-weeks post-baseline, 26-weeks post-baseline)
  • Phase 1: Change in health-related quality of life assessed by the Short-Form-12(Baseline, 10-weeks post-baseline, 14-weeks post-baseline, 26-weeks post-baseline)
  • Phase 1: Change in quality of life assessed by the EuroQol-5 Dimension-3 level (EQ-5D-3L)(Baseline, 10-weeks post-baseline, 14-weeks post-baseline, 26-weeks post-baseline)
  • Phase 1 and Phase 2: Cost of intervention arms(10-weeks (post intervention))
  • Phase 1: Use of health care resources(10-weeks post-baseline, 14-weeks post-baseline, 26-weeks post-baseline)
  • Phase 1 and Phase 2: Intervention adherence(10-weeks post-baseline)
  • Phase 2: Resistance Exercise Self-Efficacy(Baseline, 8-weeks post-baseline, 26-weeks post-baseline)
  • Phase 1: Change in social support(Baseline, 10-weeks post-baseline, 14-weeks post-baseline, 26-weeks post-baseline)
  • Phase 2: Physical Self(Baseline, 8-weeks post-baseline, 26-weeks post-baseline)
  • Phase 2: Body Functionality appreciation(Baseline, 8-weeks post-baseline, 26-weeks post-baseline)

研究者

发起方
Jenna Smith
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jenna Smith

Post Doctoral Fellow (Catherine Sabiston PI)

University of Toronto

研究点 (2)

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