Endometrial cancer survivors are a growing population with high prevalence of inactivity and obesity. Despite the benefits of strength training and the risk of functional limitations for obese individuals, interventions for this population have focused mainly on weight loss and aerobic physical activity. A small number of studies have tested resistance training, but only as part of a larger multi-modal approach; thus the specific benefits of resistance training have not been identified. Due to low long-term success rates of weight loss interventions, focusing on building strength and confidence through resistance training may be a promising approach to engaging endometrial cancer survivors in the process of health lifestyle change. The proposed pilot trial will determine the feasibility and safety of our home-based strength training intervention, which consists of an in- person instructional session followed by video coaching. All equipment is provided and all exercises can be done within the home. This home-based approach is important for preserving our reach to rural cancer survivors. Main outcomes will include adherence to the exercise sessions and the video calls, as well as participant feedback about the intervention. We will also measure anthropometrics, body composition, functional fitness, biomarkers, quality of life, and self-efficacy. However, the core purpose of a pilot study is to establish feasibility rather than to test hypotheses, therefore our specific aims focus specifically on the feasibility of both the intervention and the measures and will provide the data needed to refine our protocols to support a fully-powered trial.

Public Health Relevance

Strength training is an understudied exercise in endometrial cancer survivors with metabolic and biological implications relevant to health improvements if women can adhere to the exercise program. The proposed research will (1) establish the feasibility and safety of a 16-week home-based resistance training program of 2- 4 sessions per week, (2) measure adherence to and satisfaction with the intervention, and (3) measure the feasibility and acceptability of collection of a set of physical and psychological measures.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Small Research Grants (R03)
Project #
5R03CA230965-02
Application #
9893849
Study Section
Special Emphasis Panel (ZCA1)
Program Officer
Perna, Frank
Project Start
2019-04-01
Project End
2021-03-31
Budget Start
2020-04-01
Budget End
2021-03-31
Support Year
2
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Miscellaneous
Type
Schools of Education
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715