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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01451814
Other study ID # NCI-156241-1
Secondary ID
Status Completed
Phase Phase 2
First received October 11, 2011
Last updated March 6, 2015
Start date October 2011
Est. completion date February 2014

Study information

Verified date March 2015
Source Brown University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The primary objective of this study is to test a manualized adaptation of positive psychotherapy (PPT) for smoking cessation (PPT-S). The investigators will conduct a preliminary randomized clinical trial (N = 80) to examine the feasibility, acceptability, and efficacy of PPT-S over 26 weeks of follow up in comparison to a standard smoking cessation treatment. Both treatments will be delivered in individual 6 sessions over 6 weeks, and will include provision of transdermal nicotine patch. The effect size estimates from this Stage 1b research will provide the foundation for a future application to conduct a large-scale, Stage II, randomized clinical trial.


Recruitment information / eligibility

Status Completed
Enrollment 66
Est. completion date February 2014
Est. primary completion date February 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- smoke at least 5 cigarettes per day for longer than one year with no other ongoing tobacco product use

- willing to use the transdermal nicotine patch

- report at least a 5 on a 0 to 10 scale rating the importance of quitting smoking.

Exclusion Criteria:

- are currently experiencing psychotic symptoms, affective disorder (major depression, dysthymia, or mania) or substance use disorder (other than nicotine dependence)

- taking prescribed psychotropic medication or receiving other forms of psychotherapy

- concomitantly using other pharmacotherapies for smoking cessation

- have any contraindications for use of the transdermal nicotine patch.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Positive Psychotherapy for smoking cessation
6 sessions of individual behavioral smoking cessation counseling that incorporates techniques from Positive Psychotherapy to increase positive affect and reduce negative affect prior to and after quitting smoking. Intervention includes 8 weeks of transdermal nicotine patch.
Drug:
Nicotine polacrilex
8 weeks of nicotine patch
Behavioral:
Relaxation training
Instructions in progressive muscle relaxation
Behavioral smoking cessation treatment
Counseling on techniques to manage triggers and avoid smoking

Locations

Country Name City State
United States Center for Alcohol and Addiction Studies, Brown University Providence Rhode Island

Sponsors (2)

Lead Sponsor Collaborator
Brown University National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

References & Publications (1)

Kahler CW, Spillane NS, Day AM, Cioe PA, Parks A, Leventhal AM, Brown RA. Positive Psychotherapy for Smoking Cessation: A Pilot Randomized Controlled Trial. Nicotine Tob Res. 2015 Nov;17(11):1385-92. doi: 10.1093/ntr/ntv011. Epub 2015 Feb 2. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary 7-day Point Prevalence Smoking Abstinence at 8 Weeks Biochemically verified abstinence from smoking over the past 7 days 8 weeks No
Primary 7-day Point Prevalence Smoking Abstinence at 16 Weeks Biochemically verified abstinence from smoking over the past 7 days 16 Weeks No
Primary 7-day Point Prevalence Smoking Abstinence at 26 Weeks Biochemically verified abstinence from smoking over the past 7 days 26 Weeks No
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