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Clinical Trial Summary

This study will assess the feasibility of delivering a 12-week time-restricted eating intervention as well as the intervention's preliminary efficacy on persistent cancer-related fatigue among cancer survivors compared to a general health education control. Participants will be randomized 1:1 to one of two arms: time-restricted eating or control. Those in the intervention arm will self-select a 10-hour eating window in which to consume all food and beverages (water is allowed any time, black coffee and unsweetened tea are allowed in the morning). Both groups will receive weekly educational tips on healthy lifestyle behaviors in cancer survivorship. This study will also explore relationships between fatigue, circadian rhythm, and glucose metabolism. The hypothesis is that recruitment will be feasible, and participants will adhere to time-restricted eating and complete study activities over the course of the 12 weeks. The second hypothesis is that time-restricted eating will lead to less fatigue at 12 weeks compared to the control, accounting for baseline fatigue levels.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05256888
Study type Interventional
Source University of Maryland, Baltimore
Contact Amber Kleckner, PhD
Phone 4107065961
Email amber.kleckner@umaryland.edu
Status Recruiting
Phase N/A
Start date January 26, 2023
Completion date April 2026

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