Time-Restricted Eating and Cancer

What is the Purpose of this Study?

The purpose of this study is to evaluate whether meal timing (changing when you eat) is beneficial during active cancer treatment in reducing side effects from chemotherapy and radiation in people who have been diagnosed with rectal or breast cancer (HER2+ or triple negative). The study aims to determine whether altering an individual’s eating schedule can help shrink tumors and improve health and wellbeing. Participants will be randomly assigned to 1 of 2 groups. One group will eat within an 8-hour or shorter period daily, starting 1-3 hours after waking up. The other group will eat over a 12-hour or longer period daily. Participants will be asked to follow their eating schedule 6 days per week. Study procedures also include blood draws, questionnaires, and activity monitoring.


Eligibility

  • * Any sex/gender of any ethnic/racial background
  • * Age greater than or equal to 18 years
  • * Histologically-confirmed rectal cancer stage II, III, or IV (if curative) or human epidermal growth factor receptor 2-positive (HER2+) or triple negative breast cancer stage I, II, or III (only if definitive intent) per American Joint Committee on Cancer (AJCC) criteria
  • * BMI 18.5 kg/m2 or greater
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Where can I participate?

  • CS Cancer at Beverly Hills : Nathalie Nguyen
  • CS Cancer at Cedars-Sinai Medical Center : Nathalie Nguyen
  • Hunt Cancer Institute, an Affiliate of Cedars-Sinai Cancer
  • University of Alabama (Study Affiliate)


More about this Clinical Trial

What is the full name of this clinical trial?

IIT2020-26-FIGUEIREDO-TRE: Time-Restricted Eating and Cancer: Clinical Outcomes, Mechanisms, and Moderators

Study Details
Disease Type/Condition

Breast, Rectum

Principal Investigator

Figueiredo, Jane

Co-Investigators

Alison Quibuyen, Alma Gonzalez, Courtney M. Peterson, Gillian Gresham, Juila Levy, Jun Gong, Karen Zaghiyan, Katelyn Atkins, Kristina Bolt, Maimoona Nadri, Mitchell Kamrava, Niki Patel Tank, Sarah Salvy, Sarah Valdez, Tina Wang, Yuan Yuan

Age Group

Adult

Phase

N/A (Cancer Control)

IRB Number

STUDY00001187

ClinicalTrials.gov ID

NCT04722341

Key Eligibility
ClinicalTrials.gov

How do I learn more about this study?
Name

Nathalie Nguyen

Phone
+1 310-423-4209
Email
nathalie.nguyen@cshs.org
Study Detail
Disease Type/Condition

Breast, Rectum

Principal Investigator

Figueiredo, Jane

Age Group

Adult

Phase

N/A (Cancer Control)

IRB Number

IIT2020-26-FIGUEIREDO-TRE

ClinicalTrials.gov ID

NCT04722341

Key Eligibility
ClinicalTrials.gov

Contact
Name

Nathalie Nguyen

Phone
+1 310-423-4209
Email
nathalie.nguyen@cshs.org