Youth Smoking Cessation: Therapy +/- "The Patch"

Completed · Not applicable

Conditions studied: Smoking

In brief

Reducing tobacco use by adolescents is a national health priority. In recent polls, most adolescent smokers reported having tried unsuccessfully to quit. Smoking cessation treatment during adolescence has the potential to interrupt the progression to nicotine dependence, which is attended by a wide range of negative health consequences. Given the need for effective smoking cessation programs aimed at youth, scientifically rigorous research is warranted to reduce adolescent smoking. This project will address gaps in the scientific treatment literature. The goal of this project is to develop a tailored, practical, and efficacious smoking cessation intervention. Combined with other efforts in the field, this work can provide an initial guide to an evidence-based treatment for smoking cessation in youth. In keeping with developments in other fields of medicine, we believe that further advances in smoking cessation will move towards a goal of personalized treatment. Such an individualized approach for adolescent smoking cessation will be informed by further investigation of the relationships between outcomes in this trial. To serve these goals, we propose the following program: Youths who smoke regularly will receive a 6 week intervention using "cognitive-behavioral motivational enhancement" (CBME) supplemented by nicotine replacement therapy (NRT), if youth and parents desire this option. Furthermore, youth has to smoke more than 5 cigarettes a day in order to qualify for nicotine replacement therapy. This approach is consistent with treatment guidelines for smoking cessation (Fiore 2000). Compared with participants who fail to achieve smoking cessation, those who successfully achieve smoking abstinence during intervention, will have lower baseline rates of comorbid ADHD, lower depressive symptom scores, enhanced readiness to quit, more negative attitudes towards smoking, fewer friends who smoke, and fewer family members who smoke. The investigators predict that the intervention will help youth to quit smoking and will examine predictions of successful quitting.

Key facts

Study ID: NCT00631020
Run by: University of California, Los Angeles
People needed: 34
Starts: 2007-12-01
Expected to finish: 2009-10-01
Last updated by the study team: 2015-04-22

Who can join

Age: 14 and older, up to 21. Sex: any. Healthy volunteers: accepted.

You may qualify if…

Participants must meet all of the following inclusion criteria:
age of 14-21 years, inclusive
regular cigarette smoking at least five times a day in the month before entry into the study and initiation of smoking at least 6 months before entry
A score of 35 or greater on the Cigarette Dependence Scale-12
youth provide informed assent (for youth <18 yr) or consent (for youth ≥18 yr) and parents provide informed consent to participate in the project
documented approval to participate from the participant's treating physician for participants currently receiving treatment for a serious medical or psychiatric condition
current contact information (address, telephone number), which is needed for follow-up
able to complete study assessments and participate in the intervention (e.g., lives < 1 hr. away from the site, has family to participate in the intervention, does not have mental retardation)
youth or primary caregivers speak English or Spanish

You may not qualify if…

Participants must meet none of the following exclusion criteria in order to be eligible to receive optional nicotine replacement:
smoke less than 5 cigarettes per day
have serious cardiovascular disease, including uncontrolled hypertension, coronary artery disease, serious cardiac arrhythmias, vasospastic disease, or angina, due to potential cardiovascular effects of nicotine, as determined via the baseline medical history and physical exam
have a medical condition that could be made worse by treatment with nicotine, including poorly controlled insulin dependent diabetes, uncontrolled hyperthyroidism, pheochromocytoma, severe oropharyngeal, esophageal, or peptic ulcer disease, or severe renal or hepatic impairment as determined via the baseline medical history and physical exam
have an allergy to adhesive tape or latex or serious dermatologic disease (excluding minor skin conditions such as mild eczema) due to potential for skin allergy to patch
have a known allergy to nicotine or any component of the nicotine patches
be receiving treatment with adenosine or bupropion due to potential drug-drug interactions
be pregnant or sexually active and not using reliable birth control methods consistently (for females)

Where it is running

UCLA — Los Angeles, California, United States

Full record on ClinicalTrials.gov

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