Recruitment strategies and design considerations in a trial of resistance training to prevent dose-limiting toxicities in colon cancer patients undergoing chemotherapy

dc.contributor.authorCaan, Bette J.
dc.contributor.authorMeyerhardt, Jeffrey A.
dc.contributor.authorBrown, Justin C.
dc.contributor.authorCampbell, Kristin L.
dc.contributor.authorCespedes Feliciano, Elizabeth M.
dc.contributor.authorLee, Catherine
dc.contributor.authorRoss, Michelle C.
dc.contributor.authorQuinney, Sara
dc.contributor.authorQuesenberry, Charles
dc.contributor.authorSternfeld, Barbara
dc.contributor.authorSchmitz, Kathryn H.
dc.contributor.departmentObstetrics and Gynecology, School of Medicineen_US
dc.date.accessioned2023-05-05T15:59:15Z
dc.date.available2023-05-05T15:59:15Z
dc.date.issued2021
dc.description.abstractLow muscle is associated with an increased risk of chemotherapy-related dose limiting toxicities (DLT) in cancer patients. Resistance training (RT) improves muscle mass; however, the effects of RT on preventing DLTs and dose reductions in colon cancer patients has not been investigated. FOcus on Reducing dose-limiting toxicities in Colon cancer with resistance Exercise (FORCE) is a multicenter, randomized clinical trial examining the effects of RT on relative dose intensity (RDI; primary outcome) and moderate and severe chemotoxicities (primary outcome) in non-metastatic colon cancer patients receiving adjuvant chemotherapy. Patients (N = 180) will be recruited from Kaiser Permanente Northern California, Dana-Farber Cancer Institute, and Penn State Cancer Institute. This paper describes recruitment strategies and design considerations. Patients will be randomized in equal numbers to RT intervention or control. Patients have baseline and post completion of chemotherapy visits where information on anthropometry, physical function, body composition, quality of life, physical activity and dietary behaviors, and inflammatory blood markers will be collected. Patient-reported outcomes of chemotherapy side effects will be collected around the time of chemotherapy throughout the duration of the trial. Intervention participants will be prescribed a progressive RT program consisting of 4-6 visits with a certified exercise trainer, delivered either in-person or remotely by video conference, and will be asked to engage twice weekly in-home training sessions. Control patients at the end of the study receive a consult with a FORCE exercise trainer, an online exercise RT training program and a set of resistance bands. Results of this trial will provide information on the benefit of resistance exercise as a treatment to increase RDI.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationCaan BJ, Meyerhardt JA, Brown JC, et al. Recruitment strategies and design considerations in a trial of resistance training to prevent dose-limiting toxicities in colon cancer patients undergoing chemotherapy. Contemp Clin Trials. 2021;101:106242. doi:10.1016/j.cct.2020.106242en_US
dc.identifier.urihttps://hdl.handle.net/1805/32825
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.cct.2020.106242en_US
dc.relation.journalContemporary Clinical Trialsen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectColon canceren_US
dc.subjectChemotherapyen_US
dc.subjectChemotoxicityen_US
dc.subjectResistance trainingen_US
dc.subjectSarcopeniaen_US
dc.subjectMuscle massen_US
dc.titleRecruitment strategies and design considerations in a trial of resistance training to prevent dose-limiting toxicities in colon cancer patients undergoing chemotherapyen_US
dc.typeArticleen_US
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