Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:16 PM
Ignite Modification Date:
2026-03-26 @ 3:16 PM
NCT ID:
NCT07389603
Eligibility Criteria:
Inclusion Criteria:
* Age 18 to 60 years
* Both sexes
* Feeding window ≥14 h/day
* Usual sleep duration \>6.5 h
* Individuals diagnosed with metabolic syndrome who meet three or more of the criteria from Panel III of the National Cholesterol Education Program's Adult Treatment Guidelines:
* Waist circumference: ≥102 cm for men, ≥88 cm for women
* Triglycerides: ≥150 mg/dL or on treatment for hypertriglyceridemia
* High-Density Lipoprotein (HDL) cholesterol: \<40 mg/dL for men, \<50 mg/dL for women
* Blood pressure: systolic ≥130 mmHg and diastolic ≥85 mmHg or on treatment for hypertension
* Fasting plasma glucose: ≥100 mg/dL
* Individuals who provide informed consent
Exclusion Criteria:
* (based on participant self-report unless medical records are available)
* Pregnancy or lactation
* Currently enrolled in a weight loss program
* Current treatment with antidepressants, medications that affect glucose metabolism or appetite, or immunosuppressant therapy
* History or presence of eating disorders
* Sleep apnea
Elimination Criteria:
* Participants who do not attend more than two sessions of the psychochrononutritional intervention program.
* Participants who decide to withdraw their consent to continue in the study at any time for any reason.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
60 Years
Study:
NCT07389603
Study Brief:
Protocol Section:
NCT07389603