An exercise and nutrition intervention for ovarian cancer patients during and after first-line chemotherapy (BENITA study): a randomized controlled pilot trial. Issue 4 (2nd December 2019)

• Record Type: Journal Article
• Authors: Maurer, Tabea; von Grundherr, Julia; Patra, Stefan; Jaeger, Anna; Becher, Heiko; Schmalfeldt, Barbara; Zyriax, Birgit-Christiane; Chang-Claude, Jenny
• Is Part Of: International journal of gynecological cancer. Volume 30:Issue 4(2020)
• Page Start: 541
• Page End: 545
• Publication Date: 2019-12-02
• Subjects: ovarian cancer -- randomised controlled trial -- exercise -- nutrition; Generative organs, Female -- Cancer -- Periodicals; 616.99465
• DOI: 10.1136/ijgc-2019-000585
• Languages: English
• ISSNs: 1048-891X

Abstract

Abstract : Background: Data on the treatment-supporting effect of modifiable lifestyle factors such as nutrition and physical activity on survival or quality of life (QoL) are scarce in patients with ovarian cancer. Despite a strong rationale for evaluating the effect of a multimodal intervention and multiple studies targeting other cancer sites, randomized controlled trials (RCTs) on the effects of a combined nutrition and exercise intervention on survival and QoL in ovarian cancer patients are rare. No study has investigated the impact of an early intervention during first-line chemotherapy. Primary Objectives: To evaluate the study design, feasibility, safety, and acceptance of combined nutrition and exercise in patients diagnosed with ovarian cancer during and after first-line chemotherapy. Study Hypothesis: Physical exercise and a cancer-specific nutrition intervention after ovarian cancer diagnosis is feasible, accepted, and safe for patients receiving first-line chemotherapy. Trial Design: A 1:1 RCT with an intervention group and a control group. The intervention group receives an exercise and nutrition program whereas the control group continues to follow the usual care. Major Inclusion/Exclusion Criteria: Inclusion: women ≥18 years of age; women diagnosed with ovarian cancer, tubal cancer, or peritoneal cancer and primary or interval debulking surgery. Exclusion: Eastern Cooperative Oncology Group (ECOG) status of 2 or worse. Primary Endpoints: Recruitment rate, completion rate, side effects, and adherence. Sample Size: n=30 patients (15 per arm) will be recruited. Estimated Dates for Completing Accrual and Presenting Results: Accrual completion is planned for the end of 2019. Results will be presented in the months following study completion 1 year after recruitment has been finalised. Trial Registration Number: The pilot phase was approved by the ethics committee of the Medical Faculty of Hamburg on December 13, 2017 (PV5456). The study was registered on September 9, 2018 at the German Study Registry for Clinical Studies (DRKS00013231).