Time Restricted Eating (TRE) Among Endometrial Cancer Patients

Description

The long-term goal of this study is to determine the efficacy of Time Restricted Eating (TRE) for improving metabolic health, preventing cardiometabolic comorbidities, and improving prognosis after endometrial cancer diagnosis. The primary objective of the protocol is to conduct a 16-week randomized dietary crossover study to evaluate the feasibility, fidelity and preliminary acceptability of TRE among endometrial cancer patients, and to provide proof of principle that TRE can improve metabolic health in this population.

Conditions

Endometrial Cancer

Study Overview

Study Details

Study overview

The long-term goal of this study is to determine the efficacy of Time Restricted Eating (TRE) for improving metabolic health, preventing cardiometabolic comorbidities, and improving prognosis after endometrial cancer diagnosis. The primary objective of the protocol is to conduct a 16-week randomized dietary crossover study to evaluate the feasibility, fidelity and preliminary acceptability of TRE among endometrial cancer patients, and to provide proof of principle that TRE can improve metabolic health in this population.

Feasibility and Acceptability of Time Restricted Eating (TRE) Among Endometrial Cancer Patients: the TREND Study

Time Restricted Eating (TRE) Among Endometrial Cancer Patients

Condition
Endometrial Cancer
Intervention / Treatment

-

Contacts and Locations

Salt Lake City

Huntsman Cancer Institute, Salt Lake City, Utah, United States, 84112

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Females aged 18 years or older
  • * Diagnosed with endometrial cancer (any stage)
  • * Clinically overweight or obese (BMI \>= 25 kg/m2)
  • * At least 3 months post-cancer surgery and/or treatment
  • * Weight stable for 3 months prior to beginning the study (\<4kg weight loss/gain)
  • * Have a cell phone that is able to download a phone App and able to use phone during the day
  • * Persons with special dietary requirements
  • * Unable to provide informed consent
  • * Unable to read, write, or fill in questionnaires in English
  • * Insulin dependent diabetes
  • * Night shift workers
  • * Persons not able to use cell phone during day (like for work)

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Utah,

Mary Playdon, PhD, MPH, PRINCIPAL_INVESTIGATOR, University of Utah

Study Record Dates

2024-06