PROS Smokebusters: Adolescent Smoking Cessation in Pediatric Primary Care
Completed · Phase 1
Conditions studied: Health Care Quality, Access, and Evaluation, Smoking Cessation
In brief
This is a pilot study addressing office systems and clinician behavior change surrounding smoking cessation interventions for teens. The investigators' long-term goal is to improve the quality of clinical preventive services in practice-based research network settings. Their specific aims are to: * a) pilot procedures for recruitment and randomization of PROS practices; and b) field trial/pilot PROS practitioner cessation counseling and practices' enrollment of adolescent patients; and * assess the feasibility of pediatric clinician referral of adolescent patients to internet-based adjuncts for smoking cessation. The investigators will evaluate a pilot round of recruitment and randomization, and smoking cessation training and delivery in 10 PROS practice sites; and assess the acceptability of study procedures and on-line internet counseling adjunct referral feasibility within PROS practice sites. Up to 1000 adolescents presenting for well visits will complete a short baseline survey prior to their well-visit. A sample of them will be surveyed by phone at 4-6 weeks to provide preliminary estimates of cessation counseling effectiveness for future studies. The investigators will field test measures, describe the patterns of smoking among youth, and explore how much receiving interventions affects motivation, quitting, abstinence/relapse attitudes, attitudes towards internet-based outreach strategies, and behaviors for 100 smokers. \*\*we have completed recruitment of providers; we are recruiting teens ONLY at this point\*\*
Key facts
- Study ID
- NCT00135265
- Run by
- University of Rochester
- People needed
- 4100
- Starts
- 2006-10-01
- Expected to finish
- 2010-01-01
- Last updated by the study team
- 2010-06-28
Who can join
Age: 14 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Practitioner recruitment criteria:
- Has a patient flow of several adolescents per week.
- Reads and speaks English.
- Able and willing to provide informed consent
- Patient recruitment criteria:
- 14 years or older
- Lives in a home or apartment with access to a phone or mail address
- Speaks English
- Cognitively able to respond to survey questions
- Cognitively able to give assent and obtain parent/guardian permission or consent
You may not qualify if…
- Providers: already participating in a PROS study
Where it is running
- University of Rochester — Rochester, New York, United States
Full record on ClinicalTrials.gov
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