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Erschienen in:
05.06.2019 | Original Article
Bridging the gap: incorporating exercise evidence into clinical practice in breast cancer care
Erschienen in: Supportive Care in Cancer | Ausgabe 2/2020
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Purpose
To determine the feasibility (recruitment, retention, and adherence rates) of implementing a multi-dimensional knowledge translation (KT) intervention designed for women with breast cancer, and to explore preliminary estimates of effects of the implementation strategy on exercise level, exercise knowledge and behavior, health-related quality of life, and overall health status among breast cancer survivors.
Methods
Design: Implementation Trial. Participants: Community-dwelling women, over 18 years of age, currently undergoing chemotherapy for stage 1–3 BRCA. Randomization and Blinding: A blinded researcher randomized participants on a record-by-record basis to the intervention or control group. A researcher blinded to the group allocation of the participants conducted the statistical analysis. Intervention Group: Eight sessions of moderate intensity aerobic exercise along with eight self-management modules were delivered during chemotherapy within the cancer institution. Control Group: Usual care. Primary Outcome: Feasibility of implementation strategy measured through recruitment, retention, and adherence rates.
Results
Twenty-nine women were screened for this study. Twenty-seven met inclusion criteria and twenty-six participants were enrolled in the study. The implementation strategy was determined to be feasible and had a recruitment rate of 96%, retention rate of 100%, and adherence rate of 89%. The intervention group had significantly higher exercise levels (mean difference = 25.38, 95%CI = (9.35, 41.42)) post-intervention compared with the control group. No adverse events were reported.
Conclusions
The implementation of this KT intervention is feasible and demonstrates preliminary effects for secondary outcomes for women with breast cancer during chemotherapy. Findings support the implementation of this intervention in a multi-center trial.
Trial registration
NCT03087461