Optimization of Chrononutrition to Reduce the Risk of Disease in Shift Workers
NCT06891352 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 180
Last updated 2025-12-17
Summary
In this randomized controlled trial, the investigators will assess the health impacts of optimizing the timing of dietary consumption in nurses and nursing assistants who work night shifts, have a habitual eating window of 14 hours or more, and elevated weight. Participants will be randomized to one of three groups: (1) dietary monitoring, (2) dietary monitoring plus 10-hour daytime time-restricted eating (TRE), or (3) TRE with a low-glycemic snack during night shifts. The study includes a 2-week screening/baseline health assessment, with follow-up health assessments at 3-, 6- (primary outcome), and 12 months.
Conditions
- Night Shift Work
- Time Restricted Eating
- Overweight
- Obesity
Interventions
- BEHAVIORAL
-
Dietary Monitoring
Participants in the group will receive standard advice for a healthy lifestyle, log all food and beverage intake on the myCircadianClock app, and continue their habitual eating patterns.
- BEHAVIORAL
-
Time-Restricted Eating (TRE)
Participants in the group will receive standard advice for a healthy lifestyle, log all food and beverage intake on the myCircadianClock app, and adhere to a personalized consistent 10-hour time-restricted eating window.
- BEHAVIORAL
-
Time-Restricted Eating with a Low-Glycemic Snack (TRE-LGS)
Participants in the group will receive standard advice for a healthy lifestyle, log all food and beverage intake on the myCircadianClock app, and adhere to a personalized consistent 10-hour time-restricted eating window. On nights that participants work night shifts, they will consume a low-glycemic snack provided by the research team.
Sponsors & Collaborators
-
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
collaborator NIH -
University of San Diego
collaborator OTHER -
Salk Institute for Biological Studies
lead OTHER
Principal Investigators
-
Emily Manoogian, Ph.D. · Salk Institute for Biological Studies
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-06-02
- Primary Completion
- 2028-08-31
- Completion
- 2029-03-03
Countries
- United States
Study Locations
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