Purpose

This is a study to determine the efficacy of a smoking cessation intervention (nicotine replacement therapy (NRT) and counseling) done in a systematized manner with participants recruited from the UAB Substance Abuse Program. The definition of In Vivo experience is: use of the NRT medication during the session using specialized counseling focused around their experience of using NRT, including how the use of NRT may help them quit smoking, side effects, and smoking cessation expectancies. In this study those in the In Vivo group will put the patch on during Session 1 and given nicotine gum in Session 2 and will discuss the experience of wearing the patch or chewing the gum while they are in session. The control group will not put on the patch or chew gum during the sessions but will be given standard counseling regarding quitting smoking.

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • At least 18 years of age, - Under criminal justice supervision and expecting to remain under supervision for 9 months, - Smoked at least 5 cigarettes per day for the last 12 months, - Expire carbon dioxide (CO)> 10 ppm. - Must be able to read and speak English. - Women of child-bearing potential must be using adequate birth control.

Exclusion Criteria

  • Pregnant or breastfeeding women, - Non-English speaking, - Living in an restricted environment that does not allow smoking, - Known sensitivity to nicotine replacement or allergy to adhesive used in nicotine patches, - Cognitive impairment or major untreated mental illness that interferes with the informed consent process, - Within 6 months post-myocardial infarction or untreated severe angina, - Latex allergy, - Daily or exclusive use of other tobacco products (e.g. cigars, e-cigarettes).

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
In vivo group
Those who receive in vivo counseling and Nicotine Replacement Therapy (NRT)
  • Behavioral: In vivo counseling
    Participants in the intervention group will receive 4 in session nicotine replacement therapy and counseling focused on their experience of using NRT, including positive experiences, side effects and smoking cessation expectancies. They will also received nicotine replacement therapy (nicotine lozenge and patch) to use for smoking cessation.
Active Comparator
Controls
Standard smoking cessation counseling and Nicotine Replacement Therapy (NRT)
  • Behavioral: Standard Smoking Cessation Counseling
    Participants will receive 4 sessions of standard behavioral counseling to address their smoking. In addition, participants will received nicotine replacement therapy (Nicotine lozenge and patch) to use for smoking cessation.

Recruiting Locations

UAB Substance Abuse
Birmingham, Alabama
Contact:
Aaron Sellers, B.S.
205-917-3784
aaronsellers@uabmc.edu

More Details

Status
Recruiting
Sponsor
University of Alabama at Birmingham

Study Contact

Aaron Sellers, B.S.
205.917.3784
aaronsellers@uabmc.edu

Detailed Description

Aim 1: Compare the efficacy of an In Vivo experiential intervention to a standard treatment control group for smoking cessation. The goal of this aim will be to compare the rates of point prevalence abstinence at the 6 month post-intervention follow-up. It is expected that smokers who receive the behavioral experience of the NRT In Vivo intervention will have higher rates of abstinence at the 6 month follow-up compared to the control group. Aim 2: Compare medication adherence between groups over the 12 week intervention. The goal of this aim is to determine the impact of the In Vivo behavioral experience intervention on promoting medication adherence to NRT. It is expected that individuals in the In Vivo NRT group will have better medication adherence relative to control participants. Exploratory: Examine moderators and mediators of the experimental intervention on smoking abstinence. The goal of this aim is to explore whether demographic and smoking characteristics (e.g., sex, race, nicotine dependence, motivational status, legal charges) moderate the effect of treatment on abstinence after 12 weeks of treatment and 6-month follow-up. In addition, we will look at changes in expectancies about NRT, medication adherence, and withdrawal symptoms to determine if these changes mediate the relationship between the experimental intervention and smoking abstinence.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.