Pediatric Residency Training On Tobacco

NCT00098215 | Unknown Phase 2

• 2 other identifiers: 1R01HD40683-11R01HD040683
• Study Type: interventional
• Target: 4,000
• Locations: 1 country
• Sites: 14

Brief Summary

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.

Conditions

Tobacco Use Disorder

Keywords

Residency training

Interventions

Pediatric residency training on tobacco BEHAVIORAL

Eligibility Criteria

• Age: 0 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

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.

Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.

Sponsors & Collaborators

• Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD): lead

Study Sites (14)

UMDNJ-Robert Wood Johnson Medical School

Camden, New Jersey, 08103-1489, United States

RECRUITING

Mount Sinai School of Medicine (Jersey City Program)

Jersey City, New Jersey, 07304, United States

RECRUITING

Jersey Shore Medical Center

Neptune City, New Jersey, 07754, United States

RECRUITING

Newark Beth Israel Medical Center

Newark, New Jersey, 07112, United States

RECRUITING

St. Joseph's Hospital and Medical Center

Paterson, New Jersey, 07503, United States

RECRUITING

Long Island College Hospital

Brooklyn, New York, 11201, United States

RECRUITING

Woodhull Medical and Mental Health Center

Brooklyn, New York, 11206-5317, United States

RECRUITING

Brooklyn Hospital Center Program

Brooklyn, New York, 11212, United States

RECRUITING

Nassau County Medical Center

East Meadow, New York, 11554, United States

RECRUITING

New York Flushing Hospital Medical Center

Flushing, New York, 11355, United States

RECRUITING

Winthrop-University Hospital Program

Mineola, New York, 516-663-2288, United States

RECRUITING

New York and Presbyterian Hospital (Cornell Campus) Program

New York, New York, 10021, United States

RECRUITING

Lincoln Medical Center

The Bronx, New York, 10451, United States

RECRUITING

Bronx/Lebanon Hospital

The Bronx, New York, 10457, United States

RECRUITING

MeSH Terms

Conditions

Tobacco Use Disorder

Condition Hierarchy (Ancestors)

Substance-Related Disorders; Chemically-Induced Disorders; Mental Disorders

Study Officials

• Joseph Schwab, M.D.

  New Jersey Medical School

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: ECT
• Intervention Model: PARALLEL
• Sponsor Type: NIH

Study Record Dates

• First Submitted: December 3, 2004
• First Posted: December 6, 2004
• Study Start: March 1, 2001
• Study Completion: February 1, 2006
• Last Updated: November 10, 2005

Record last verified: 2004-12

Locations

US (14)