- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00064922
Incentive Programs for Female Substance Abusers Who Smoke - 3
January 11, 2017 updated by: National Institute on Drug Abuse (NIDA)
Incentive Programs for Female Substance Abusers Who Smoke
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
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.
Study Type
Interventional
Enrollment
90
Phase
- Phase 2
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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California
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Los Angeles, California, United States, 90061
- Shields for Families, Inc.
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
15 years to 99 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Leslie Amass, Ph.D., Los Angeles Treatment Research Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2002
Primary Completion (Actual)
April 1, 2006
Study Completion (Actual)
April 1, 2006
Study Registration Dates
First Submitted
July 15, 2003
First Submitted That Met QC Criteria
July 15, 2003
First Posted (Estimate)
July 16, 2003
Study Record Updates
Last Update Posted (Estimate)
January 12, 2017
Last Update Submitted That Met QC Criteria
January 11, 2017
Last Verified
May 1, 2008
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NIDA-13638-3
- R01-13638-3
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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