search
Back to results

Incentive Programs for Female Substance Abusers Who Smoke - 3

Primary Purpose

Tobacco Use Disorder

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Behavior Therapy
Sponsored by
National Institute on Drug Abuse (NIDA)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tobacco Use Disorder focused on measuring nicotine dependence

Eligibility Criteria

15 Years - 99 Years (Child, Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Pregnant and or post-partum with at least one child under 1 year old living with them, or non-pregnant, non-post-partum females or previous participant in this study protocol Nicotine Dependent as confirmed by DSM-IV checklist Current cigarette smoker Breath CO reading of at least 8 ppm at the time of the initial study screening Current client with the Shields for Families (Shields) treatment programs Exclusion Criteria: Non-smoker

Sites / Locations

  • Shields for Families, Inc.

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
July 15, 2003
Last Updated
January 11, 2017
Sponsor
National Institute on Drug Abuse (NIDA)
search

1. Study Identification

Unique Protocol Identification Number
NCT00064922
Brief Title
Incentive Programs for Female Substance Abusers Who Smoke - 3
Official Title
Incentive Programs for Female Substance Abusers Who Smoke
Study Type
Interventional

2. Study Status

Record Verification Date
May 2008
Overall Recruitment Status
Completed
Study Start Date
January 2002 (undefined)
Primary Completion Date
April 2006 (Actual)
Study Completion Date
April 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute on Drug Abuse (NIDA)

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to examine the effects of incentive programs for the treatment of nicotine dependence in women who have problems with substance dependence.
Detailed Description
This study will determine the influence of voucher-based CM on reducing smoking (and other drug) use during pregnancy or in post-partum women with children under 1 year of age living with them, or in non-pregnant females who smoke. We are targeting smoking cessation since cigarette use is so prevalent in our service. We will compare a control group to two different voucher-based contingent-reinforcement procedures: one that targets smoking abstinence alone vs. one that offers additional incentives for negative BAL and urinalysis results.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tobacco Use Disorder
Keywords
nicotine dependence

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Enrollment
90 (false)

8. Arms, Groups, and Interventions

Intervention Type
Behavioral
Intervention Name(s)
Behavior Therapy

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Pregnant and or post-partum with at least one child under 1 year old living with them, or non-pregnant, non-post-partum females or previous participant in this study protocol Nicotine Dependent as confirmed by DSM-IV checklist Current cigarette smoker Breath CO reading of at least 8 ppm at the time of the initial study screening Current client with the Shields for Families (Shields) treatment programs Exclusion Criteria: Non-smoker
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leslie Amass, Ph.D.
Organizational Affiliation
Los Angeles Treatment Research Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Shields for Families, Inc.
City
Los Angeles
State/Province
California
ZIP/Postal Code
90061
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Incentive Programs for Female Substance Abusers Who Smoke - 3

We'll reach out to this number within 24 hrs