- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00297440
Exercise, Smoking Cessation and Adolescents
July 22, 2010 updated by: Temple University
Exercise to Aid Smoking Cessation in Adolescent Girls
We seek to: 1) conduct the formative work to adapt the cessation materials and exercise protocol from focus on adult women to adolescent girls, and 2) conduct a small randomized pilot trial to determine the preliminary efficacy of the intervention in a sample of adolescent girls.
Therefore, this study, will serve as a pilot for a larger clinical trial.
Successful smoking cessation in adolescent girls could contribute to the future reduction of chronic disease morbidity and mortality in this group.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
Approximately 22% of youth currently smoke cigarettes despite the increased risk of cancer and cardiovascular disease associated with cigarette use.
Tobacco use continues to be the leading, preventable cause of mortality among US adults.
Research has shown that those who smoke their first cigarette between the ages of 14-26 are more likely to become nicotine dependent, and, therefore, more resistant to smoking cessation efforts, than those initiating smoking at a later age.
Although the smoking prevalence among girls declined in the 1970's and 1980's, the current smoking rates among high school girls has held constant from 1998 to 2000.
Despite the negative health consequences associated with smoking, weight concerns and fear of weight gain have been shown to be associated with the uptake of smoking in girls.
Alternatively, exercise has been shown to be a positive health behavior, and can provide the same perceived benefits of smoking: self-esteem, relaxation, weight management.
In previous trials in adult women, vigorous intensity exercise has been shown to be effective for aiding with smoking cessation.
Therefore, this study will adapt the efficacious group-based cognitive behavioral smoking cessation treatment plus exercise to meet the needs of adolescent girls.
This project will consist of two phases.
In Phase I of this project, 4 focus groups will be conducted (each consisting of 8-10 adolescent girls) to adapt the intervention.
Adaptations will include making the materials, intervention content, and language age-appropriate and relevant for youth.
Phase II of the project will consist of a randomized pilot study in which 40 adolescent girls will be randomly assigned to: a) standard cognitive-behavioral smoking cessation plus exercise (CBT+Exercise) or b) standard cessation with equal contact time (Standard+Contact).
The sample will be recruited, treated for 12 weeks and followed for 3 months.
Smoking cessation outcome (continuous abstinence) will be validated by saliva cotinine.
Exercise adherence will be validated by attendance at supervised sessions, and objective monitoring.
Secondary analysis of proposed theoretical mediators of behavior change will be conducted, including weight concerns and self-efficacy.
The primary hypothesis is that girls in the CBT+Exercise group will have higher quit rates than girls in the Standard+Contact group.
In summary, we seek to: 1) conduct the formative work to adapt the cessation materials and exercise protocol from a focus on adult women to adolescent girls, and 2) conduct a small randomized pilot trial to determine the preliminary efficacy of the intervention in a sample of adolescent girls.
Therefore, this study will serve as a pilot for a larger clinical trial.
Successful smoking cessation in adolescent girls could contribute to the future reduction of chronic disease mortality in this group.
Study Type
Interventional
Enrollment (Anticipated)
80
Phase
- Phase 2
- Phase 1
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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Rhode Island
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Providence, Rhode Island, United States, 02903
- The Miriam Hospital
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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
13 years to 19 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Parental consent will be required for participation in the project
Exclusion Criteria:
- For Phase I of the study, we will recruit adolescent girls who report smoking at least 5 cigarettes per day for 6 months. We will recruit approximately 40 girls to participate in one of 4 focus groups. For Phase II, we will recruit adolescent female smokers (n = 40) aged 13-19. Potential participants for Phase II must smoke at least 5 cigarettes per day and be sedentary (i.e., participating in physical activity two days per week or less for 30 minutes or less each day). Other specific eligibility requirements for both phases include: a) having no physical or mental limitations that would restrict their ability to be active or complete study measures; b) passing the Physical Activity Readiness Questionnaire (PAR-Q).
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
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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Smoking status
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Secondary Outcome Measures
Outcome Measure |
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Weight
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Physical Activity
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Body image
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Melissa A Napolitano, PhD, The Miriam Hospital
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
March 1, 2006
Primary Completion (Actual)
August 1, 2009
Study Completion (Anticipated)
August 1, 2011
Study Registration Dates
First Submitted
February 27, 2006
First Submitted That Met QC Criteria
February 27, 2006
First Posted (Estimate)
February 28, 2006
Study Record Updates
Last Update Posted (Estimate)
July 23, 2010
Last Update Submitted That Met QC Criteria
July 22, 2010
Last Verified
July 1, 2010
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- R03CA119712 (U.S. NIH Grant/Contract)
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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