Yale School of Medicine
New Haven, Connecticut, 06519, United States
NCT Number: NCT05157698
This study will compare the effectiveness of behavioral and pharmacologic treatment, alone and combined, for improvements in weight loss, cardiovascular risk factors, and psychosocial functioning following metabolic and bariatric surgery.
This study is active but is not currently recruiting participants.
Notify Me18 year–70 year
All sexes
Interventional
Phase 3
New Haven, Connecticut, 06519, United States
Metabolic and bariatric surgery is currently the most effective treatment for severe obesity; however, a substantial proportion of patients attain suboptimal weight losses and continue to struggle with obesity, weight regain, and related medical comorbidities after surgery. Thus, this study aims to perform a randomized double-blind placebo-controlled study to test the effectiveness of a rigorous manualized behavioral weight loss treatment and a FDA-approved weight loss agent (naltrexone+bupropion), alone and in combination, for improving weight loss, cardiovascular risk factors, and psychosocial functioning after metabolic and bariatric surgery. This study will produce important new clinical findings regarding the utility and effectiveness of pharmacotherapy and behavioral weight loss for a rapidly growing obesity subgroup and will inform care models for managing chronic and refractory obesity to enhance outcomes after metabolic and bariatric surgery.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants in this intervention will take active naltrexone and bupropion pills.
Participants in this intervention will receive behavioral weight loss treatment.
Participants in this intervention will take inactive (placebo) pills.
Time frame: Baseline to after the 6-month treatment
BMI is calculated using measured height and weight
Time frame: From post-treatment (6-months) to the 12-month follow-up
BMI is calculated using measured height and weight
Time frame: From baseline at study enrollment to after the 6-month treatment
Total cholesterol will be measured by bloodwork.
Time frame: From post-treatment (6-months) to the 12-month follow-up
Total cholesterol will be measured by bloodwork.
Time frame: From baseline at study enrollment to after the 6-month treatment
HbA1C will be measured by bloodwork.
HbA1C
Time frame: From post-treatment (6-months) to the 12-month follow-up
HbA1C will be measured by bloodwork.
HbA1C
Time frame: From baseline at study enrollment to after the 6-month treatment
Glucose will be measured by bloodwork.
Time frame: From post-treatment (6-months) to the 12-month follow-up
Glucose will be measured by bloodwork.
Time frame: From baseline interview at study enrollment to after the 6-month treatment
Loss-of-control eating frequency is a continuous variable of loss-of-control eating episodes .during the past 28 days assessed using the Eating Disorder Examination interview
Time frame: From post-treatment (6-months) to the 12-month follow-up
Loss-of-control eating frequency is a continuous variable of loss-of-control eating episodes during the past 28 days assessed using the Eating Disorder Examination interview.
Time frame: From baseline interview at study enrollment to after the 6-month treatment
Eating-disorder psychopathology is a continuous variable as assessed by the global score of the Eating Disorder Examination/Eating Disorder Examination-Questionnaire. Scores range from 0-6 (0=no eating-disorder psychopathology; 6=severe eating-disorder psychopathology).
Time frame: From post-treatment (6-months) to the 12-month follow-up
Eating-disorder psychopathology is a continuous variable as assessed by the global score of the Eating Disorder Examination/Eating Disorder Examination-Questionnaire. Scores range from 0-6 (0=no eating-disorder psychopathology; 6=severe eating-disorder psychopathology).
Time frame: From baseline interview at study enrollment to after the 6-month treatment
Food craving is a continuous variable of food craving as assessed by the Food Craving Inventory. Scores range from 0-5 (0=no food craving; 5=greatest food craving).
Time frame: From post-treatment (6-months) to the 12-month follow-up
Food craving is a continuous variable of food craving as assessed by the Food Craving Inventory. Scores range from 0-5 (0=no food craving; 5=greatest food craving).
Time frame: From baseline interview at study enrollment to after the 6-month treatment
Depressive Symptoms [ Time Frame: From baseline interview at study enrollment to after the 6-month treatment ] Depressive symptoms is a continuous variable of depressive symptomatology as assessed by the self-report measure, the Patient Health Questionnaire - 9. Total scores range from 0-27 (0=no depressive symptoms, 27=greater depressive symptoms).
Depressive symptoms is a continuous variable of depressive symptomatology as assessed by the self-report measure, the Patient Health Questionnaire - 9. Total scores range from 0-27 (0=no depressive symptoms, 27=greater depressive symptoms).
Time frame: From post-treatment (6-months) to the 12-month follow-up
Depressive Symptoms [ Time Frame: From baseline interview at study enrollment to after the 6-month treatment ] Depressive symptoms is a continuous variable of depressive symptomatology as assessed by the self-report measure, the Patient Health Questionnaire - 9. Total scores range from 0-27 (0=no depressive symptoms, 27=greater depressive symptoms).
Depressive symptoms is a continuous variable of depressive symptomatology as assessed by the self-report measure, the Patient Health Questionnaire - 9. Total scores range from 0-27 (0=no depressive symptoms, 27=greater depressive symptoms).
Yale University
Other
Behavioral and Pharmacological Treatments to Enhance Weight Outcomes After Metabolic and Bariatric Surgery
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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