Obesity Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People of any racial or ethnic background
- People with a body mass index (a measure of height-to-weight ratio) between 20 and 34.9
- People who sleep an average of 7 hours or more per night, as measured over a 2-week screening period
- People who eat something within 1 hour of waking up on at least 5 days per week
- People whose midpoint of sleep falls at 4 AM or earlier (for example, someone who sleeps from 10 PM to 6 AM, with a midpoint of 2 AM)
Who may not be able to join:
- People who had fewer than 10 nights of at least 7 hours of sleep during the 2-week screening period
- People who nap regularly during the day
- People who have a current or past sleep disorder, or who score above 10 on a standard insomnia severity scale
- People who have a current or past psychiatric condition, including eating disorders or seasonal affective disorder
- People with any mental health condition that could interfere with the study results
- People who currently smoke cigarettes, use tobacco products, e-cigarettes, or vapes, or who stopped smoking less than 3 years ago
- People who work night shifts or rotating shifts
- People who have travelled across time zones within 4 weeks before the study
- People with a history of drug or alcohol misuse, or who regularly drink more than 3 alcoholic drinks per day (men) or more than 2 per day (women)
- People whose weight has changed by more than 5% in the past 3 months, who are currently on a diet or weight loss program, or who have had any weight loss procedure
- People who are pregnant or who gave birth less than 1 year ago
- People who have been diagnosed with sleep apnea, or who score highly on a standard sleep apnea risk questionnaire
- People with depression (based on a standard scoring scale) or who are taking antidepressant medications
- People with restless leg syndrome or circadian rhythm disorders
- People with dementia or cognitive impairments
- People currently taking medications that affect mood, mental state, or sleep
- People taking ongoing pain relief or anti-inflammatory medications
- People who have had gastrointestinal surgery, including gastric bypass surgery
- People with restricted or disordered eating patterns based on a standard eating behaviour questionnaire
- People who are unable to have an MRI scan for any reason
- People with a low red blood cell measure (haematocrit below 30%) (confirm with trial site)
- People taking beta blocker medications, as these can interfere with a hormone involved in the study
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Marie-Pierre St-Onge, PhD, Columbia University
Phone: 212 305 9379
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Energy expenditure; Body composition; Nutritional intakes
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.