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Tests a circadian lifestyle plan for adults with obesity and short sleep

Tests a plan limiting night light and late snacks in adults with obesity.

Plain-language title generated from the registry record
Registry title: Circadian Intervention to Improve Cardiometabolic Health

Key facts

Where
Salt Lake City, United StatesSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 18-45 with overweight or obesity who usually sleep less than 6.5 hours a night. It tests a daily-habit program about light at night and after-dinner snacks.

Age
18-45 years
Sex
Men and women; the trial wants equal numbers of men and women.
Disease stage
Body mass index (BMI) 25.0-34.9 kg/m2. Usual sleep under 6.5 hours per night for the last 6 months.
Earlier treatment
Cannot be in a weight loss or physical activity program, such as the Diabetes Prevention Program.

Main reasons for not taking part

  • A diagnosed sleep disorder or major psychiatric illness
  • Significant organ disease, such as diagnosed diabetes, heart disease or kidney disease
  • Shift work now or within the last year
  • Weight change of more than 10% of body weight in the last six months
  • Pregnant, planning pregnancy, breastfeeding, or in or past menopause

Read by machine on 9 November 2026.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 45 years old?

Source: NCT05943626, who can take part

Where in United States

  • College of Health Research Complex--University of UtahSalt Lake City, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
University of Utah
Trial code
NCT05943626
Record updated
5 August 2026
Original description
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).Read full original descriptionShow less

Timing of Circadian Synchronizers: The TOCS Study

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).

Inclusion: Age: 18-45 years old; equal numbers of men and women; Body mass index (BMI): 25.0-34.9 kg/m2,; Sleep Habits: habitual self-reported average total sleep time (TST) <6.5 hours per night for prior 6 months.

Exclusion: Weight change: >10% of body weight over prior six months; Clinically diagnosed sleep disorder or major psychiatric illness; Evidence of significant organ dysfunction or disease (e.g., diagnosed diabetes, cardiovascular disease, or kidney disease); Shift-work: current or history of within last year; Current enrollment in weight loss or physical activity program like the Diabetes Prevention Program; Use of prescription drugs or substances known to influence sleep or glucose metabolism; Experiencing menopause or post-menopausal; Currently pregnant or planning to become pregnant, or currently lactating; Currently smoking; Alcohol intake >3 drinks per day or >14 drinks per week.

ClinicalTrials.gov NCT05943626