Trials / Completed
CompletedNCT01061528
Coping Skills Treatment for Smoking Cessation
Distress Tolerance Treatment for Smoking Cessation
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 116 (actual)
- Sponsor
- Butler Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Accepted
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.
Detailed description
1. 18-65 years of age, 2. a regular smoker for at least one year, 3. currently smoking 10 or more cigarettes per day, 4. report motivation to quit smoking in the next month.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Transdermal Nicotine | Participants will use the full strength 21mg. patch for 4 weeks, will taper to the 14 mg. patch for the next 2 weeks, and then to the 7 mg. patch for the remaining 2 weeks of treatment. |
Timeline
- Start date
- 2009-09-01
- Primary completion
- 2013-08-01
- Completion
- 2013-10-01
- First posted
- 2010-02-03
- Last updated
- 2018-10-16
- Results posted
- 2018-06-15
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01061528. Inclusion in this directory is not an endorsement.