Comparative Study of SR Bupropion for Adolescent Smoking Cessation

Smoking Cessation Clinical Trial

Official title: Randomized, Double-Blind, Placebo-Controlled Trial of SR Bupropion for Adolescent Smoking Cessation

Status Not yet recruiting

Clinical Trial Summary

Bupropion has been used successfully and safely for smoking cessation in adults. It was also used in very few studies among adolescent population. Our hypothesis is that Bupropion would be effective and safe among the adoelscent psychiatric population. A double-blind randomized controlled-trial will be held to determine that.

Clinical Trial Description

The study will be conducted in Geha Mental Health Center. A total of 80 adolescent non-psychotic smokers will be recruited for this study. A smoker is defined as a cosumer of at least 5 cigarettes daily. A total of 80 patients will be recruited from the adolescent psychiatric wards or the adolescent clinics of the mental health center. The study group (N=40) will receive bupropion SR and the control group (N=40) will receive placebo medication. Age of participants will range from 13-20 years. Both genders will be included and all ethnic origins.

All participants will receive a detailed explanation about the study, its aims, the bupropion therapy, including possible adverse effects of the drug and other possible therapeutic alternatives. They will receive a leaflet summarizing all relevant data and information. Then they and their parents will sign an informed consent to participate in the study.

Procedure The mental health center's pharmacist will encapsulate the bupropion tablets, which will be supplied by the manufacturing company. The study capsules will all be kept in the hospital's pharmacy. Randomization will be performed using a random number table. The code will be held solely by the principal investigator, and will be broken in the end of the study's follow-up period, unless an emergency occurs. All participants will be given the telephone number of the principal investigator for any questions or problems arising.

The subjects in both groups will be double-blindly randomized to receive either bupropion or placebo. The assignment to each group will be done randomly in order to ensure location concealment. For subjects receiving bupropion, the dose will be 150 mg/d for the first three days, increasing for 150 mg twice daily, continued for a period of eight weeks. In case of intolerable side effects, the dosage will be decreased to 150 mg daily.

On recruitment, all subjects will be screened for-

• Medical history

• Vital signs

• Height

• Weight

• Place of birth

• Tobacco use history

• Alcohol and substance abuse

• Elctrocardiogram (ECG)

• Urine pregnancy test (for girls only)

• Kiddie schedule for affective disorders and schizophrenia (K-SADS-PL) screening tool (37).

Possible electrocardiographic side effects of bupropion that have been reported in the literature were tachycardia and conduction delays (widened QRS complex and/or prolonged QTc interval), but none of these delays progressed to a life-threatening arrhythmia, even in case of overdose.

Exclusion criteria will be:

• Psychiatric disorders in Axis I of DSM IV (38) (for the control group)

• Smoking less than 6 cigarettes a day

• Using other tobacco products other than cigarettes

• Using any other smoking cessation treatment

• Exhaled CO level of less than 10 ppm

• Convulsive disorder or a history of seizures

• A first-degree relative with a convulsive disorder

• Past sensitivity to bupropion.

• Positive pregnancy test

• lactation

• A lack of motivation to quit smoking

• Alcohol and substance abuse (or current alcohol withdrawal)

• Mental retardation and a lack of ability to give an informed consent

• Concurrent use of Monoamine oxidase inhibitors (MAO-I).

• Anorexia nervosa or bulimia nervosa.

All subjects will be evaluated for weight, smoking, substance use, anxiety and depressive symptoms at baseline, 1 month, 3 months, 6 months and 1 year. Follow-up phase will be blinded as well. Evaluation in these time points will include:

• Fagerstrom Tolerance Questionnaire modified for adolescents (FTQ( to measure nicotine dependence (39).

• Quantitive information on tobacco, alcohol and drug use (timeline followback methods)

• Children depression inventory (CDI) (40) to measure depression, translated and validated to hebrew (41).

• Children depression rating scale (CDRS) (42) to measure depression, translated and validated to hebrew (41)

• The Screen for Child Anxiety Related Emotional Disorders (SCARED) to measure anxiety (43;44)

• Exhaled air carbon monoxide (CO)

• Urine cotinine In addiction to the pharmacological therapy, both groups of the study will receive supportive and psychoeducational treatment in the setting of group therapy. Supportive psychotherapy focuses on using suggestions and supportive expressions to encourage the patient in his goal of quitting smoking. Psychoeducational treatment concentrates on educating the patients on the benefits of abandoning smoking and the use informative details in regards to that issue.

Main outcome measures: (1) Smoking cessation for 3 months. (2) Decrease in the carving to smoke. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Smoking
• Smoking Cessation

• NCT number: NCT00819078
• Study type: Interventional
• Source: Geha Mental Health Center
• Contact: Gal Shoval, M.D.
• Phone: 972-3-9258258
• Email: shovgal@tau.ac.il
• Status: Not yet recruiting
• Phase: N/A
• Start date: January 2009
• Completion date: January 2014