Status:

COMPLETED

Strategies to Avoid Returning to Smoking

Lead Sponsor:

University of Pittsburgh

Collaborating Sponsors:

National Institute on Drug Abuse (NIDA)

Conditions:

Smoking

Eligibility:

FEMALE

14+ years

Phase:

NA

Brief Summary

The purpose of this study is to evaluate the relative efficacy of a postpartum smoking relapse prevention program, Strategies to Avoid Returning to Smoking (STARTS), and a supportive, nondirective com...

Detailed Description

The goal of the proposed investigation is to determine whether a cognitive behavioral relapse prevention intervention designed to address mood and weight concerns during the postpartum period will dec...

Eligibility Criteria

Inclusion

  • Women will be eligible to participate if they:
  • report having smoked daily for at least one month during the 3 months prior to becoming pregnant;
  • smoked at least 10 cigarettes per day before quitting;
  • report no smoking in the four weeks prior to enrollment;
  • are not currently smoking as verified by a CO less than 8ppm;
  • are at least 'somewhat' motivated to remain abstinent postpartum and
  • are at least 14 years of age.

Exclusion

  • Women with current, acute psychiatric disorders, including other substance use problems and symptoms that warrant immediate treatment will be referred for care and excluded from this trial.
  • Women with psychiatric disorders (e.g., depressive or anxiety disorders), who are not acutely suicidal and in whom the symptoms are not severe enough to preclude participation in a randomized trial, will be eligible to participate. However, women taking psychiatric medications that may affect the mediators of treatment, such as antidepressant, anxiolytic or weight control medications, will be excluded from participation.
  • Women who endorse current suicidality will be discussed immediately with the consulting physician and referred to the psychiatric emergency room for further evaluation as indicated.

Key Trial Info

Start Date :

September 1 2007

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2014

Estimated Enrollment :

300 Patients enrolled

Trial Details

Trial ID

NCT00757068

Start Date

September 1 2007

End Date

June 1 2014

Last Update

May 27 2015

Active Locations (1)

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1

UPMC

Pittsburgh, Pennsylvania, United States, 15213