PROS Brief Smoking Cessation Counseling in Pediatric Practice to Reduce Secondhand Smoke Exposure of Young Children
This study has been completed.
Sponsor:
University of Rochester
Collaborators:
American Legacy Foundation
Robert Wood Johnson Foundation
Information provided by:
University of Rochester
ClinicalTrials.gov Identifier:
NCT00135213
First received: August 23, 2005
Last updated: December 20, 2007
Last verified: September 2006
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Purpose
The investigators' long-term goal is to improve the quality of services targeting the prevention of secondhand smoke (SHS). Their specific aims are to:
- refine components of office systems and counseling interventions for parental tobacco control in pediatric outpatient settings; and
- pilot test the feasibility and efficacy of a parental tobacco control randomized controlled trial in pediatric office settings using 5 intervention and 5 comparison pediatric practice sites.
The investigators hypothesize that:
- clinicians in intervention practices (compared to those in control practices) will more often implement successful office systems, screen for parental smoking, advise parents to quit and to prohibit smoking and SHS exposure at home, recommend pharmacotherapy, provide adjuncts, and refer parents to cessation programs; and
- parents who smoke in intervention practices (measured by 3-month follow-up telephone surveys) will be more likely than those in control practices to have received cessation services, use pharmacotherapy, make lasting quit attempts, and institute rules to prohibit smoking and limit SHS exposure at home.
| Condition | Intervention | Phase |
|---|---|---|
|
Health Care Quality, Access, and Evaluation Smoking Cessation |
Behavioral: training in smoking cessation |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Prevention |
| Official Title: | PROS Brief Smoking Cessation Counseling in Pediatric Practice to Reduce Secondhand Smoke Exposure of Young Children |
Resource links provided by NLM:
Further study details as provided by University of Rochester:
Primary Outcome Measures:
- rates of reduced exposure to secondhand smoke
| Estimated Enrollment: | 1200 |
| Study Start Date: | October 2005 |
| Study Completion Date: | July 2007 |
The investigators' long-term goal is to improve the quality of services targeting the prevention of secondhand smoke (SHS). Their specific aims are to:
- refine components of office systems and counseling interventions for parental tobacco control in pediatric outpatient settings; and
- pilot test the feasibility and efficacy of a parental tobacco control randomized controlled trial in pediatric office settings using 5 intervention and 5 comparison pediatric practice sites.
The investigators hypothesize that:
- clinicians in intervention practices (compared to those in control practices) will more often implement successful office systems, screen for parental smoking, advise parents to quit and to prohibit smoking and SHS exposure at home, recommend pharmacotherapy, provide adjuncts, and refer parents to cessation programs; and
- parents who smoke in intervention practices (measured by 3-month follow-up telephone surveys) will be more likely than those in control practices to have received cessation services, use pharmacotherapy, make lasting quit attempts, and institute rules to prohibit smoking and limit SHS exposure at home.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- PROS practices will be eligible to participate if they are located in a community-based setting with a non-institutionalized population.
- Physicians are eligible if they are able and willing to provide informed consent and have a patient flow of several children per week, and are not currently participating in another PROS study. They also must be able to read and speak English.
Eligible parents will:
- be parents or guardians age 18 or older;
- be parents of a child aged 0-6;
- have access to a telephone; and
- be able to speak/read English.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00135213
Locations
| United States, New York | |
| University of Rochester | |
| Rochester, New York, United States, 14642 | |
Sponsors and Collaborators
University of Rochester
American Legacy Foundation
Robert Wood Johnson Foundation
Investigators
| Principal Investigator: | Jonathan D Klein, MD, MPH | University of Rochester |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00135213 History of Changes |
| Other Study ID Numbers: | 11585 |
| Study First Received: | August 23, 2005 |
| Last Updated: | December 20, 2007 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of Rochester:
|
passive smoking pediatric practice smoking cessation |
Additional relevant MeSH terms:
|
Smoking Habits |
ClinicalTrials.gov processed this record on October 16, 2012
