MedPath

Impact of Semaglutide on Tobacco Use and Related Health Behaviors

Phase 4
Recruiting
Conditions
Tobacco Use
Interventions
Drug: Placebo
Registration Number
NCT06986993
Lead Sponsor
University of Oklahoma
Brief Summary

This pilot randomized trial will assess the impact of 12 weeks of semaglutide administration (vs placebo) on changes in: (i) tobacco use and related factors (nicotine craving, withdrawal, motivation to quit, etc.) and (ii) biological biomarkers of health (e.g., epigenetics, glucose variability via continuous glucose monitoring \[CGM\], etc.) in adult smokers with obesity (n = 40). We will integrate molecular biology procedures (e.g., epigenetics) to maximize internal validity with real-world smartphone-based ecological momentary assessment (EMA) surveys to maximize external validity

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
SemaglutideSemaglutideParticipants will be randomized to receive active semaglutide or placebo (saline) injection once a week for 12weeks
PlaceboPlaceboParticipants will be randomized to receive active semaglutide or placebo (saline) injection once a week for 12weeks
Primary Outcome Measures
NameTimeMethod
Cigarette smoking12 weeks

Changes in number of cigarettes smoked per day

Secondary Outcome Measures
NameTimeMethod
Weight12 weeks

change in weight (in lbs)

Trial Locations

Locations (1)

Health Promotion Research Center

🇺🇸

Oklahoma City, Oklahoma, United States

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