RT Journal Article
SR Electronic
T1 An exercise and nutrition intervention for ovarian cancer patients during and after first-line chemotherapy (BENITA study): a randomized controlled pilot trial
JF International Journal of Gynecologic Cancer
JO Int J Gynecol Cancer
FD BMJ Publishing Group Ltd
SP 541
OP 545
DO 10.1136/ijgc-2019-000585
VO 30
IS 4
A1 Tabea Maurer
A1 Julia von Grundherr
A1 Stefan Patra
A1 Anna Jaeger
A1 Heiko Becher
A1 Barbara Schmalfeldt
A1 Birgit-Christiane Zyriax
A1 Jenny Chang-Claude
YR 2020
UL http://ijgc.bmj.com/content/30/4/541.abstract
AB 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).