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N/A N=116 Randomized Single-blind Treatment

Coping Skills Treatment for Smoking Cessation

Nicotine Dependence

Enrolled (actual)
116
Serious AEs
0.0%
Results posted
Jun 2018
Primary outcome: Primary: Number of Participants With Biochemically Verified Smoking Abstinence — 11; 12 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Transdermal Nicotine (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Butler Hospital
Primary completion
Aug 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Biochemically Verified Smoking Abstinence
11; 12

Summary

The primary purpose of this study is to evaluate the efficacy of a new type of exposure- and acceptance-based smoking cessation treatment vs. standard behavioral smoking cessation treatment, in conjunction with the use of the transdermal nicotine patch. In both treatments, participants will receive one 60-minute individual session, seven 2-hour group sessions and two individual brief telephone contacts over an eight-week period. Both treatments include 8 weeks of transdermal nicotine patch, which will begin at the time of quitting smoking and will continue after the treatment sessions have ended. Participants will provide follow-up data with regard to their smoking status through a one-year follow-up period.

Eligibility Criteria

Inclusion Criteria

  • 18-65 years old
  • regular smoker for at least one year
  • currently smoking 10 or more cigarettes per day

Exclusion Criteria

  • Current Axis I disorder
  • Psychoactive substance abuse or dependence (excluding nicotine dependence) within past year
  • Current suicidal risk
  • Pregnancy or breast feeding
  • Use of nicotine replacement products or bupropion
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01061528). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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