Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Increasing Contingency Management Success in Smoking Cessation
This study is currently recruiting participants.
Verified by The University of Texas Health Science Center at San Antonio, April 2007
Sponsors and Collaborators: The University of Texas Health Science Center at San Antonio
National Institutes of Health (NIH)
Information provided by: The University of Texas Health Science Center at San Antonio
ClinicalTrials.gov Identifier: NCT00273793
  Purpose

Incentives can be used to facilitate the acquistion of many healthy behaviors, such as smoking cessation. However, there is much remove for improvement in the use of incentives. This study investigates how two aspects of providing incentives influence the effectiveness of using incentives to promote smoking cessation. One aspect is the criterion for providing incentives, e.g., whether to require smoking cessation before providing an incentive or to provide incentives following smoking reductions. The other aspect being investigated is whether it is best to use a fixed incentive amount or an amount that increases with continued cessation success.


Condition Intervention
Smoking
Behavioral: Contingency Management

MedlinePlus related topics: Quitting Smoking Smoking
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: Increasing Contingency Management Success Using Shaping

Further study details as provided by The University of Texas Health Science Center at San Antonio:

Primary Outcome Measures:
  • Breath Carbon Monoxide levels indicating smoking abstinence during the study, and at follow-up six months after study entry

Secondary Outcome Measures:
  • cigarrettes reported smoked

Estimated Enrollment: 240
Study Start Date: June 2005
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Criteria

Inclusion Criteria: Daily Smokers smoking a pack or more of cigarettes a day who are able to report to the study site each work day for about 5 minutes for around 3 months. Subjects must also have a breath CO level indicative of smoking at this level, and most report smoking for at least two years. Subjects must intend on quiting smoking.

-

Exclusion Criteria: Participation in another study by this group within the past year. Inability to give informed consent. Incapable of attendance each workday during the morning hours.

-

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00273793

Contacts
Contact: Floyd Jones 210-567-5462 JonesFA@UTHSCSA.edu

Locations
United States, Texas
Smoking Cessation Laboratory, Department of Psychiatry, UTHSCSA, 7703 Floyd Curl Drive Recruiting
San Antonio, Texas, United States, 78229-3900
Contact: Floyd A Jones     210-567-5462     JonesFA@UTHSCSA.edu    
Principal Investigator: Richard J Lamb, Ph.D.            
Sponsors and Collaborators
The University of Texas Health Science Center at San Antonio
Investigators
Principal Investigator: Richard J Lamb, Ph.D. University of Texas
  More Information

Study ID Numbers: 045-0013-195, RO1 DA013304
Study First Received: January 4, 2006
Last Updated: April 17, 2007
ClinicalTrials.gov Identifier: NCT00273793  
Health Authority: United States: Food and Drug Administration

Study placed in the following topic categories:
Smoking

Additional relevant MeSH terms:
Habits

ClinicalTrials.gov processed this record on January 16, 2009