Development of a MHBC Intervention for Weight Loss and Smoking Cessation for Pre-Bariatric Surgery Patients

Part of paid clinical trials in New Haven, Connecticut.

Sponsor
Yale University
Study ID
NCT07224087
Phase
PHASE1
Status
Recruiting

Conditions

  • Bariatric Surgery Patients
  • Obesity
  • Smoking Cessation

Eligibility Criteria

Sex
ALL
Age
18 Years - 65 Years
Healthy Volunteers
Not accepted

Interventions

  • Naltrexone Hydrochloride — DRUG
    Participants will be given 50mg/day of Naltrexone for 4 months.
  • Bupropion HCl Extended Release — DRUG
    Participants will be given 300mg/day of Bupropion for 4 months. Bupropion will be taken twice daily (150mg in the morning, followed by 150mg in the late afternoon/early evening).
  • Cognitive-Behavioral Therapy — BEHAVIORAL
    Participants will receive cognitive-behavioral therapy for weight loss and smoking cessation. Participants will meet with their assigned study clinician weekly for 60 minutes for 4 months.

Study Details

The purpose of this research study is to develop and pilot a multiple health behavior change intervention for weight loss and smoking cessation using medication (Naltrexone + Bupropion) and behavior therapy in adults seeking bariatric surgery.

Key Dates

Start date
Mar 2, 2026
Status verified
Mar 2026
Primary completion
Dec 31, 2027
Completion
Dec 31, 2027

Study Design

Enrollment
20 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Intervention
    Participants will receive the multiple health behavior change intervention with combined medication (Naltrexone 50mg/day; Bupropion Extended Release 300mg/day) and behavior therapy (Cognitive-Behavioral Therapy) for 4 months.

Primary Outcome Measure

Study enrollment to assess Feasibility [ Time Frame: 16 weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Yale UniversityNew HavenConnecticut06511
Caitlin E Smith, PhD
203-785-7210

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