Rinad S Beidas1, Breah Paciotti1, Fran Barg1, Andrea R Branas1, Justin C Brown1, Karen Glanz1, Angela DeMichele1, Laura DiGiovanni1, Domenick Salvatore1, Kathryn H Schmitz2. 1. Department of Psychiatry (RSB), Department of Family Medicine and Community Health (BP, FB, KHS), Abramson Cancer Center (AB, KG, AD, LD, DS, KHS), and Center for Clinical Epidemiology (JCB, KG, AD, LD, DS, KHS), University of Pennsylvania Perelman School of Medicine, Philadelphia, PA; Good Shepherd Penn Partners, Philadelphia, PA (AB); Biobehavioral Health Science Department, School of Nursing, University of Pennsylvania, Philadelphia, PA (KG). 2. Department of Psychiatry (RSB), Department of Family Medicine and Community Health (BP, FB, KHS), Abramson Cancer Center (AB, KG, AD, LD, DS, KHS), and Center for Clinical Epidemiology (JCB, KG, AD, LD, DS, KHS), University of Pennsylvania Perelman School of Medicine, Philadelphia, PA; Good Shepherd Penn Partners, Philadelphia, PA (AB); Biobehavioral Health Science Department, School of Nursing, University of Pennsylvania, Philadelphia, PA (KG). Schmitz@upenn.edu.
Abstract
BACKGROUND: The primary aims of this hybrid Type 1 effectiveness-implementation trial were to quantitatively assess whether an evidence-based exercise intervention for breast cancer survivors, Strength After Breast Cancer, was safe and effective in a new setting and to qualitatively assess barriers to implementation. METHODS: A cohort of 84 survivors completed measurements related to limb volume, muscle strength, and body image at baseline, 67 survivors completed measurements 12 months later. Qualitative methods were used to understand barriers to implementation experienced by referring oncology clinicians and physical therapists who delivered the program. RESULTS: Similar to the efficacy trial, the revised intervention demonstrated safety with regard to lymphedema, and led to improvements in lymphedema symptoms, muscular strength, and body image. Comparison of effects in the effectiveness trial to effects in the efficacy trial revealed larger strength increases in the efficacy trial than in the effectiveness trial (P < .04), but few other differences were found. Qualitative implementation data suggested significant barriers around intervention characteristics, payment, eligibility criteria, the referral process, the need for champions (ie, advocates), and the need to adapt during implementation of the intervention, which should be considered in future dissemination and implementation efforts. CONCLUSIONS: This trial successfully demonstrated that a physical therapy led strength training program for breast cancer survivors can be implemented in a community setting while retaining the effectiveness and safety of the clinical trial. However, during the translation process, strategies to reduce barriers to implementation are required. This new program can inform larger scale dissemination and implementation efforts.
RCT Entities:
BACKGROUND: The primary aims of this hybrid Type 1 effectiveness-implementation trial were to quantitatively assess whether an evidence-based exercise intervention for breast cancer survivors, Strength After Breast Cancer, was safe and effective in a new setting and to qualitatively assess barriers to implementation. METHODS: A cohort of 84 survivors completed measurements related to limb volume, muscle strength, and body image at baseline, 67 survivors completed measurements 12 months later. Qualitative methods were used to understand barriers to implementation experienced by referring oncology clinicians and physical therapists who delivered the program. RESULTS: Similar to the efficacy trial, the revised intervention demonstrated safety with regard to lymphedema, and led to improvements in lymphedema symptoms, muscular strength, and body image. Comparison of effects in the effectiveness trial to effects in the efficacy trial revealed larger strength increases in the efficacy trial than in the effectiveness trial (P < .04), but few other differences were found. Qualitative implementation data suggested significant barriers around intervention characteristics, payment, eligibility criteria, the referral process, the need for champions (ie, advocates), and the need to adapt during implementation of the intervention, which should be considered in future dissemination and implementation efforts. CONCLUSIONS: This trial successfully demonstrated that a physical therapy led strength training program for breast cancer survivors can be implemented in a community setting while retaining the effectiveness and safety of the clinical trial. However, during the translation process, strategies to reduce barriers to implementation are required. This new program can inform larger scale dissemination and implementation efforts.
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