Strengthening Instrumental Extinction to Prevent Smoking Relapse (VLNCCue)

Completed · Not applicable

Conditions studied: Cigarette Smoking

In brief

The central objective of the project is to evaluate the effect of incorporating smoking related contexts into very low nicotine content (VLNC) cigarette extinction trials on clinically relevant, smoking-related outcomes. Adult smokers interested in quitting smoking (N=80) will be interviewed and trained to take pictures where they smoke cigarettes. Following taking these pictures, participants will then be switched to smoke VLNCs while wearing a 21 mg/d nicotine patch (EXT) for three weeks. During this 3-week treatment period, half of the sample (n=40) will be randomly assigned to undergo six, 60-minute sessions of multiple context extinction (MCE+) during which they will view smoking-related environments and smoke their assigned cigarettes. The remaining 40 participants will undergo control MCE (exposure to nature environments; MCE-) and smoke their assigned cigarettes. At the end of the three weeks, participants will quit smoking and continue to wear the nicotine patch while being followed during a 10-week abstinence period. Participants will also complete a follow-up phone call 6 months after their quit day.

Key facts

Study ID

NCT02538042

Run by

Francis McClernon, Ph.D.

People needed

87

Starts

2015-10-08

Expected to finish

2017-09-08

Last updated by the study team

2018-11-14

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• generally healthy (i.e. ambulatory, not currently sick)
• interest in quitting smoking
• smoking of at least 5 cig/day of a brand delivering ≥ 0.5 mg nicotine (FTC method) for > 1 year
• an expired carbon monoxide concentration of at least 10 ppm (to confirm inhalation) or urinary cotinine > 1000 ng/mL to confirm daily smoking (NicAlert=6)

You may not qualify if…

• inability to attend all required experimental sessions
• desire to quit smoking prior to the study quit date
• a quit attempt resulting in greater than 3 days of abstinence in the past 30 days
• report of significant health problems including but not restricted to (e.g. chronic hypertension, emphysema, seizure disorder, history of significant heart problems)
• unstable psychiatric conditions (any significant change in psychiatric symptoms during the past 3 months as determined by the study physician)
• schizophrenia and schizoaffective disorder
• psychiatric medication changes (e.g. new prescriptions, changes in dosages, or discontinuation of medications) in the past 3 months that was a result of negative changes in symptoms
• use of other tobacco products or e-cigarettes more than 9 days in the past 30 days
• current alcohol or drug abuse
• use of illegal drugs (excluding marijuana) or drugs without a valid prescription as measured by urine drug screen
• current use of nicotine replacement therapy or other smoking cessation treatment
• use of Theophylline for asthma
• presence of conditions contraindicated for nicotine replacement therapy (e.g., skin allergies)
• previous participation in a study within the past year involving use of Spectrum cigarettes
• systolic BP greater than or equal to 140 (participants failing for blood pressure will be allowed to rescreen once)
• diastolic BP greater than or equal to 90 (participants failing for blood pressure will be allowed to rescreen once)
• heart rate greater than or equal to 100 (participants failing for heart rate will be allowed to rescreen once)
• blood alcohol level >0.0 (participants failing the blood alcohol screen will be allowed to rescreen once)
• pregnant, trying to become pregnant, or breastfeeding

Where it is running

• Duke Medical Center — Durham, North Carolina, United States

Full record on ClinicalTrials.gov

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