Combination Nicotine Replacement for Alcoholic Smokers

Smoking Clinical Trial

Official title:

Combination Nicotine Replacement for Alcoholic Smokers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00064844
• Other study ID #: NIAAACOO11197-05
• Secondary ID: R01AA011197
• Status: Completed
• Phase: Phase 4
• Start date: August 2002
• Est. completion date: July 2006

Study information

• Verified date: August 2021
• Source: Yale University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The overall objective of the study is to develop recommendations for treatment programs to help alcoholic smokers to stop smoking. A sample of 175 alcohol dependent cigarette smokers will be recruited from the community and treated in a 6-month outpatient alcohol and tobacco treatment program. The 175 patients will be divided into two groups. One group will receive an active nicotine patch and active nicotine gum. The other group will receive an active nicotine patch and placebo nicotine gum. Followup assessments will be conducted for 1-year from the beginning of treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 96
• Est. completion date: July 2006
• Est. primary completion date: July 2006
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion criteria:

• Males and females at least 18 years old.

• English speaking.

• Meets criteria for alcohol dependence or alcohol abuse.

• Must complete an alcohol detoxification program prior to entering the study.

• Currently smoking 15 or more cigarettes per day and have at least a 3 year history of smoking.

• Have a current desire to stop smoking and stop drinking.

• Willing to complete followup assessments up to 12 months after treatment.

• Willing to provide names of 2 people who can help locate the subject at followup and the name of one person who can verify information about alcohol and tobacco use.

• One person per household.

Exclusion Criteria:

• Allergy to nicotine patch or nicotine gum.

• Weigh less than 100 pounds.

• Use other nicotine products, such as cigars, pipes or smokeless tobacco.

• Severe skin disorder.

• Active peptic ulcer.

• Active joint disease.

• Heart attack within 3 months prior to entering the study.

• Pregnant or breastfeeding female who are not on birth control.

• Currently taking medication to treat alcoholism or smoking, such as naltrexone, disulfiram or bupropion.

• Poor vision or hearing that would interfere with using a cell phone.

• Lack of transportation to the treatment site or live at least one hour from the treatment site.

• Homeless.

Related Conditions & MeSH terms

• Alcoholism
• Smoking

Intervention

Behavioral:
• Cognitive Behavior Therapy for alcohol and smoking cessation
Individual 60-minute treatment sessions were scheduled weekly for the first 3 months, then monthly for the next 3 months for a total of 16 sessions. Alcohol treatment was based on the cognitive behavioral therapy manual developed for Project MATCH, with approximately 40-45 minutes of each session devoted to alcohol treatment. Components of this intervention included identifying alcohol antecedents, coping with alcohol urges, managing thoughts about alcohol, problem solving, drink refusal skills, planning for emergencies, communication and assertiveness training and enhancing social support networks for alcohol abstinence. The smoking cessation intervention was delivered in the same sessions as the alcohol treatment, with approximately 15-20 minutes of each session devoted to smoking cessation. Treatment employed behavioral elements that have been supported empirically according to the USDHHS smoking cessation practice guideline.

Drug:
• Nicoderm CQ nicotine patch
Subjects in both arms were instructed to use one 21-mg (Nicoderm CQ®) nicotine patch daily for 8 weeks followed by one 14-mg patch daily for 2 weeks, then followed by one 7-mg patch daily for 2 weeks, for a total of 12 weeks of nicotine patch therapy.
• Placebo gum
Placebo gum was given for ad libitum use, with encouragement to use at least six pieces per day, up to a maximum of 20 pieces per day. The placebo gum (manufactured by Fertin Pharma A/S, Vejle, Denmark) contained 2.6% cayenne pepper to simulate the taste of nicotine. Use of the gum was encouraged for 24 weeks.
• Nicotine gum - Nicorette®
Nicotine gum (2 mg uncoated mint Nicorette®) was given for ad libitum use, with encouragement to use at least six pieces per day, up to a maximum of 20 pieces per day. Use of the gum was encouraged for 24 weeks.

Locations

Country	Name	City	State
United States	VA Connecticut Healthcare System	Newington	Connecticut

Sponsors (2)

Lead Sponsor	Collaborator
Yale University	National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Country where clinical trial is conducted

United States, 

References & Publications (2)

Cooney NL, Cooney JL, Perry BL, Carbone M, Cohen EH, Steinberg HR, Pilkey DT, Sevarino K, Oncken CA, Litt MD. Smoking cessation during alcohol treatment: a randomized trial of combination nicotine patch plus nicotine gum. Addiction. 2009 Sep;104(9):1588-96. doi: 10.1111/j.1360-0443.2009.02624.x. Epub 2009 Jun 22. — View Citation

Holt LJ, Litt MD, Cooney NL. Prospective analysis of early lapse to drinking and smoking among individuals in concurrent alcohol and tobacco treatment. Psychol Addict Behav. 2012 Sep;26(3):561-72. doi: 10.1037/a0026039. Epub 2011 Oct 24. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	6 Month Smoking Abstinence	Percentage of participants with prolonged carbon monoxide verified smoking abstinence	6 months after smoking quit date
Primary	12 Month Smoking Abstinence	Percentage of participants with prolonged carbon monoxide verified smoking abstinence	12 months after smoking quit date