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NCT00435344 Clinical Trial

Provider and Peer Delivered Youth Smoking Intervention

Tobacco Dependence Clinical Trial

Official title:
Provider and Peer Delivered Youth Smoking Intervention

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00435344
Other study ID # 1R01CA080254-01A1
Secondary ID
Status Completed
Phase Phase 2
First received February 12, 2007
Last updated February 12, 2007
Start date February 1999
Est. completion date January 2004

Study information
Verified date February 2007
Source University of Massachusetts, Worcester
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study was to determine whether a pediatric practice-based smoking prevention and cessation intervention increases abstinence rates among adolescents.

Description:

The majority of adolescent smokers are interested in quitting and have attempted to stop with limited success. A recent review of cessation trials for adolescents has concluded that there are no proven programs to help teens stop smoking, but suggested interventions based on cognitive behavioral therapy and sensitive to stages of change appear promising. The American Academy of Pediatrics suggests that pediatricians are well-positioned to intervene with adolescent smokers, as well as with nonsmokers to prevent initiation. A comprehensive, practice-based smoking prevention and cessation intervention for adolescents delivered by pediatric providers and peer counselors in the context of routine care has the potential for assisting nonsmoking adolescents in remaining smoke-free and smoking adolescents to quit.

Recruitment information / eligibility
Status Completed
Enrollment 2711
Est. completion date January 2004
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 13 Years to 17 Years
Eligibility Inclusion Criteria:

- Aged 13 to 17, regardless of smoking status

- Scheduled for routine or acute care office visit

- Parental consent and youth assent

Exclusion Criteria:

- Unable to complete study requirements

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• Pediatric Practice-Based Smoking Intervention

Locations
Country Name City State
United States University of Massachusetts Medical School Worcester Massachusetts

Sponsors (1)
Lead Sponsor Collaborator
University of Massachusetts, Worcester

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Abstinence from smoking in the past 30 days at 6 months and 1 year
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