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Implementing physical activity for individuals with cancer during treatment: protocol for the IMPACT implementation–effectiveness trial
Implementing physical activity for individuals with cancer during treatment: protocol for the IMPACT implementation–effectiveness trial
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Implementing physical activity for individuals with cancer during treatment: protocol for the IMPACT implementation–effectiveness trial
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Implementing physical activity for individuals with cancer during treatment: protocol for the IMPACT implementation–effectiveness trial
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Implementing physical activity for individuals with cancer during treatment: protocol for the IMPACT implementation–effectiveness trial
Implementing physical activity for individuals with cancer during treatment: protocol for the IMPACT implementation–effectiveness trial
Journal Article

Implementing physical activity for individuals with cancer during treatment: protocol for the IMPACT implementation–effectiveness trial

2025
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Overview
IntroductionThe prevalence of cancer in Canada is growing, leading to multiple lasting side effects in survivors. The physical and psychosocial benefits of regular physical activity (PA) during and after treatment for individuals with cancer are well established, however, not well implemented in a clinical setting. The overall aim of this project is to build on previous work and conduct a multicentred randomised controlled trial (RCT) and evaluate the effectiveness of a novel implementation strategy using PA and self-management versus usual care during cancer treatment.Methods and analysisStudy design: a hybrid implementation–effectiveness RCT will occur at five cancer centres across Ontario, Canada. Participants: eligible participants include adults with a cancer diagnosis (any type or stage) who are receiving treatment and cleared for exercise by their oncology care team. Intervention: participants (n=129) will be randomised to one of three groups: (1) institution-based exercise and self-management (SM) (eight in-person sessions of aerobic exercise and eight SM modules), (2) SM alone (SM only: eight virtual modules) or (3) usual care (no intervention). Outcomes: the Reach, Effectiveness, Adoption, Implementation and Maintenance framework will assess implementation outcomes. The primary effectiveness outcome is self-report PA level postintervention. Data analysis: outcomes will be measured at four time points (baseline, postintervention, 6- and 12-month follow-up). Descriptive statistics will be used to present implementation outcomes. An analysis of covariance will assess change between groups over time.Ethics and disseminationFindings from this trial will build on previous work and inform the way PA services are provided within cancer institutions across Ontario, Canada, and inform decision-making on how to incorporate exercise evidence into real-world clinical practice in cancer care. The Hamilton Integrated Research Ethics Board (ID: 7673 & 17454) has approved this study. Results will be disseminated using a combination of peer-reviewed publications, conference presentations and community organisation presentations. Participants will contribute to dissemination by sharing ‘participant perspectives’, highlighting their experience in the project and thoughts on the implementation strategies used.Trial registration numberThe study is registered on clinicaltrials.gov (ID: NCT06323707).