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RECRUITING
NCT05943626
NA

Circadian Intervention to Improve Cardiometabolic Health

Sponsor: University of Utah

View on ClinicalTrials.gov

Summary

The overall goal is to examine the efficacy of a circadian intervention in people with overweight and obesity and habitual short sleep duration (HSSD). Participants will undergo a randomized controlled trial, with circadian intervention and control (healthy lifestyle) groups. The circadian intervention is designed to reduce nighttime light exposure and after-dinner snack food intake. Alternatively, the control group will receive basic health information (e.g., physical activity, goal setting, and nutrition when eating out).

Official title: Timing of Circadian Synchronizers: the TOCS Study

Key Details

Gender

All

Age Range

18 Years - 45 Years

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2023-06-13

Completion Date

2026-03

Last Updated

2024-12-20

Healthy Volunteers

Yes

Interventions

BEHAVIORAL

Circadian Intervention

The circadian intervention group will receive counseling and instruction to reduce evening and nighttime light exposure, increase morning room light and sunlight exposure, and to finish all food consumption at least 4 hours before bedtime.

Locations (1)

College of Health Research Complex--University of Utah

Salt Lake City, Utah, United States