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ADAPT Study: Assessing Diet, Appetite and Physiology Throughout Weight Loss Study)
RECRUITINGN/ASponsored by University of Washington
Actively Recruiting
PhaseN/A
SponsorUniversity of Washington
Started2023-10-01
Est. completion2027-07-31
Eligibility
Age18 Years – 60 Years
Healthy vol.Accepted
Locations2 sites
View on ClinicalTrials.gov →
NCT06174389
Summary
Behavioral weight loss programs for obesity can result in weight loss and health benefits. However, behavioral weight loss often stops despite efforts to continue losing weight, this can be called an involuntarily weight loss plateau. This study investigates changes in metabolism and/or the brain that contribute to the occurrence of an involuntary weight loss plateau.
Eligibility
Age: 18 Years – 60 YearsHealthy volunteers accepted
Inclusion Criteria: * BMI 30.0 - 50.0 kg/m2 * Able to attend study intervention classes and study visits/assessments * Independently living with access to food preparation facilities Exclusion Criteria: * Current smoker or regular use of nicotine containing products and/or cannabis * Heavy alcohol use (≥2 drinks/d for females, ≥3 drinks/d for males) or drug use * Known cognitive impairments or h/o stroke * Type 2 diabetes (known diagnosis or by screening A1c (≥6.5%)) * Medical conditions (chronic diseases, cancer, MS) or labs limiting ability to participate * Females: currently pregnant (or 6-months postpartum of full-term pregnancy) and/or current breastfeeding * Use of medications with significant effects on appetite (e.g., weight loss medications, atypical antipsychotics, stimulants) and/or chronic use of anticoagulants * History of bariatric surgery * History of eating disorder * Current participation in a formal weight loss program * Prior or current participation in a research study involving weight loss * Weight-reduced by \>10% within past year * Weight \> 330 pounds (MRI limit) * Allergy or intolerance to or unwillingness to consume study foods provided at visit * MRI contraindication (e.g., implanted metal, claustrophobia) * Do not have a phone compatible with activity tracker or access to videoconferencing platform that will be used for the dietary intervention or other appropriate technology needed to complete study procedures * Any condition(s) found by the study team and confirmed with the PI(s) that make it unsafe to participate
Conditions2
ObesityWeight Loss
Locations2 sites
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Actively Recruiting
PhaseN/A
SponsorUniversity of Washington
Started2023-10-01
Est. completion2027-07-31
Eligibility
Age18 Years – 60 Years
Healthy vol.Accepted
Locations2 sites
View on ClinicalTrials.gov →
NCT06174389