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Clinical Trials/NCT00135213
NCT00135213
Completed
Phase 1

PROS Brief Smoking Cessation Counseling in Pediatric Practice to Reduce Secondhand Smoke Exposure of Young Children

University of Rochester1 site in 1 country1,200 target enrollmentOctober 2005

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Health Care Quality, Access, and Evaluation
Sponsor
University of Rochester
Enrollment
1200
Locations
1
Primary Endpoint
rates of reduced exposure to secondhand smoke
Status
Completed
Last Updated
18 years ago

Overview

Brief Summary

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.

Detailed Description

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.

Registry
clinicaltrials.gov
Start Date
October 2005
End Date
July 2007
Last Updated
18 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility 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.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

rates of reduced exposure to secondhand smoke

Study Sites (1)

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