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NCT07618117Not yet recruiting

Improving Sleep Health and Circadian Timing to Support Cardiometabolic Health in Adolescents

Mitigating Cardiometabolic Risk by Improving Sleep Health and Circadian Timing in Adolescents With Overweight/Obesity

Source: ClinicalTrials.gov · Last updated 1 Jun 2026

Brief summary (registry, in English)

Many teenagers get too little and late timed sleep. High body weight and diabetes are increasing in teenagers as well. This study plans to learn more about whether improving sleep habits can help improve how the body regulates blood sugar and energy use in teenagers who have higher body weight. To answer this question, the investigators plan to enroll teenagers who get \<7 hours of sleep on school nights and measure changes in blood sugars and energy use after two weeks of typical sleep (sleeping on their normal school schedule) and two weeks of a sleep intervention that includes spending longer time in bed at night, melatonin, and morning light.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
13 May 2026
Start date
25 Aug 2026
Primary completion date
15 Jun 2030
Lead sponsor
University of Colorado, Denver
Diseases
Obesity
NCT number
NCT07618117

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 25 Aug 2026 to the primary completion date, 15 Jun 2030
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Regular use of medications affecting sleep or insulin sensitivity (e.g., stimulants, sleep aids, systemic steroids, insulin sensitizers, GLP-1 agonists)

Other illness

  • Reported diagnosis of sleep disorder (e.g., insomnia, obstructive sleep apnea)
  • IQ\<70 or severe mental illness that may impact sleep or study participation (e.g., schizophrenia), eating disorder, or active suicidal ideation

Lab values

  • Medical comorbidities that impact sleep or insulin sensitivity (e.g., diabetes \[based on history or screening HbA1c\])

Other

  • Schedules that would preclude participants from adhering to the sleep schedules (e.g., night-shift employment)

Who the study is looking for

  • High school students between 14-19 years
  • Overweight/obesity (BMI \>85% for age and sex)
  • Have habitually insufficient sleep, defined as ≤ 7 hours per night on school days
  • Habitually inactive (≤ 3 h of physical activity reported per week)
  • Tanner stage 4 or 5, based on breast development for girls and testicular size for boys.

Age in the registry: 14 years to 19 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.