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Pediatric Residency Training On Tobacco

Pediatric Residency Training on Tobacco

The purpose of this study is to determine whether a specialized, technology-based training program in tobacco prevention is more effective than standard training for pediatric residents who counsel youth and their parents.

Studie Overzicht

Toestand

Onbekend

Gedetailleerde beschrijving

The American Academy of Pediatrics and other leading health agencies call upon pediatricians to address environmental tobacco smoke (ETS), prevent smoking onset in youths, and encourage cessation of tobacco use by adolescents and their parents. Systematic intervention on tobacco by pediatricians would protect infants and young children from the harmful effects of ETS and save adolescents from a lifetime of addiction and tobacco-related disease. Despite this, few pediatricians address tobacco use, and pediatric residency training programs are not preparing residents to play a leadership role in the anti-tobacco arena.

The Pediatric Residency Training on Tobacco project is a four-year randomized controlled study of the efficacy of a specialized tobacco intervention program for pediatric residents. Eight participating pediatric training sites were randomly assigned to a Special Training condition featuring "Solutions for Smoking", a hybrid CD-ROM/Website training program. Six sites were randomly assigned to a control condition that provided standard print literature. Key features of "Solutions for Smoking" include a website containing background material on tobacco, interviewing, behavioral and pharmacological aspects of intervention, and a series of CD-ROMs containing audio-visual vignettes that model state-of-the-art interviewing and tobacco intervention skills. Residents are expected to practice the interventions with patients in their Continuity Clinics, and all sites are provided with brochures and other intervention materials for this purpose. Study investigators meet with residents at all sites three times per year to discuss the program and the residents' efforts to intervene on tobacco with their patients. Annually, second and third-year residents participate in Objective Structured Clinical Examinations (OSCEs) and a Resident Tobacco Survey. Patients and parents attending each of the Continuity Clinics complete Patient and Parent Tobacco Surveys at baseline and end of study.

Primary endpoints include changes over time in pediatric residents' tobacco intervention knowledge, skills, and activities as reported on the Tobacco Surveys and measured by performance on the OSCEs at baseline and follow-up. Secondary endpoints include changes in smoking, other tobacco use, and control of ETS by patients and parents. The study hypothesizes that pediatric residents in both arms of the study will be similar in knowledge and skills at baseline; that residents in the specialized training program will acquire more knowledge and greater skills for tobacco intervention during the course of the study compared to residents in the control condition; and residents in each condition will increase the frequency in which they address tobacco in patients and parents.

Studietype

Ingrijpend

Inschrijving

4000

Fase

  • Fase 2

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • New Jersey
      • Camden, New Jersey, Verenigde Staten, 08103-1489
      • Jersey City, New Jersey, Verenigde Staten, 07304
        • Werving
        • Mount Sinai School of Medicine (Jersey City Program)
        • Contact:
      • Neptune, New Jersey, Verenigde Staten, 07754
        • Werving
        • Jersey Shore Medical Center
        • Contact:
      • Newark, New Jersey, Verenigde Staten, 07112
        • Werving
        • Newark Beth Israel Medical Center
        • Contact:
          • Joshua S Rosenblatt, MD
          • Telefoonnummer: 973-926-7040
          • E-mail: josh@bethi.com
      • Paterson, New Jersey, Verenigde Staten, 07503
        • Werving
        • St. Joseph's Hospital and Medical Center
        • Contact:
    • New York
      • Bronx, New York, Verenigde Staten, 10451
        • Werving
        • Lincoln Medical Center
        • Contact:
          • Hermann Mendez, MD
          • Telefoonnummer: 718-780-1025
      • Bronx, New York, Verenigde Staten, 10457
        • Werving
        • Bronx/Lebanon Hospital
        • Contact:
          • Ronald Bainbridge, MD
          • Telefoonnummer: 718-518-5760
      • Brooklyn, New York, Verenigde Staten, 11201
        • Werving
        • Long Island College Hospital
        • Contact:
          • Umit Emre, MD
          • Telefoonnummer: 718-780-1025
      • Brooklyn, New York, Verenigde Staten, 11206-5317
        • Werving
        • Woodhull Medical and Mental Health Center
        • Contact:
          • John Moohr, MD
          • Telefoonnummer: 718-963-8778
      • Brooklyn, New York, Verenigde Staten, 11212
        • Werving
        • Brooklyn Hospital Center Program
        • Contact:
          • Theodoros Raptis, MD
          • Telefoonnummer: 718-250-6209
          • E-mail: mjs9005@nyp.org
      • East Meadow, New York, Verenigde Staten, 11554
        • Werving
        • Nassau County Medical Center
        • Contact:
          • Stephen P Katz, MD
          • Telefoonnummer: 516-572-6177
      • Flushing, New York, Verenigde Staten, 11355
        • Werving
        • New York Flushing Hospital Medical Center
        • Contact:
          • Fatema Meah, MD
          • Telefoonnummer: 718-670-3145
      • Mineola, New York, Verenigde Staten, 516-663-2288
        • Werving
        • Winthrop-University Hospital Program
        • Contact:
          • Stephen Marino, DO
          • Telefoonnummer: 516-663-4423
      • New York City, New York, Verenigde Staten, 10021
        • Werving
        • New York and Presbyterian Hospital (Cornell Campus) Program
        • Contact:
          • Susan Bostwick, MD
          • Telefoonnummer: 212-746-3522

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

1 seconde en ouder (Kind, Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Ja

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

The training program will include all residents enrolled in the 14 participating residency training programs.

The Baseline and Follow-up Resident Tobacco Surveys and OSCEs will include all second and third year residents enrolled in the residency training programs at baseline and years 1, 2, and 3 of follow-up.

The Baseline and Follow-up Patient Tobacco Survey will include 30 patients, ages 12-21, who were present in the waiting areas of the Continuity Clinic when the surveys were administered. All patients present in the clinic will be approached and invited to participate. Partcipants must be able to read English or Spanish, and patients who are attending the clinic for the very first time will not be eligible to participate in the survey.

The Baseline and Follow-up Parent Tobacco Surveys will be administered to 100 parents (one per family) who are present in the clinic when the surveys are administered. Parents who cannot read English or Spanish and who are bringing their child to the clinic for the very first time will not be able to participate.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Educatief/Counseling/Training
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Joseph Schwab, M.D., New Jersey Medical School

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

1 maart 2001

Studie voltooiing

1 februari 2006

Studieregistratiedata

Eerst ingediend

3 december 2004

Eerst ingediend dat voldeed aan de QC-criteria

3 december 2004

Eerst geplaatst (Schatting)

6 december 2004

Updates van studierecords

Laatste update geplaatst (Schatting)

10 november 2005

Laatste update ingediend die voldeed aan QC-criteria

9 november 2005

Laatst geverifieerd

1 december 2004

Meer informatie

Termen gerelateerd aan deze studie

Trefwoorden

Andere studie-ID-nummers

  • 1R01HD40683-1

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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