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NCT00380510 Clinical Trial

The Safe Teen Study

Prevention Clinical Trial

Official title:
The SAFE TEEN Study: Family Physicians' Reports of Facilitators of and Barriers to Preventive Care for Adolescents.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00380510
Other study ID # HP000016-02
Secondary ID
Status Completed
Phase N/A
First received September 25, 2006
Last updated September 25, 2006
Start date June 2004
Est. completion date February 2005

Study information
Verified date September 2006
Source The University of Texas Health Science Center at San Antonio
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The study examines (1)the incidence of preventive health services provided by family physicians to adolescent patients, and (2)barriers and facilitators of prevention discussions between family physicians and their adolescent patients.

Description:

This study used a card study design to allow volunteer physicians to record research data in the context of providing clinical care. The method was brief, simple, and convenient for busy practicing clinicians.

Volunteer resident physicians and faculty carried data collection checklists in their pockets and completed one for every adolescent patient seen during a randomly selected two week period. Physicians attempted to collect data on ten consecutive encounters with teen patients aged 11-21 years. The checklist documented patient characteristics (age, gender and ethnicity), reason for visit, parent presence, and types of prevention issues discussed during the visit. Patient and visit information was collected to assess its influence on physician prevention discussions. Finally, the checklist asked open-ended questions related to barriers to and facilitators to teen prevention discussions.

The study involved five clinical sites comprising approximately 140 faculty and resident family physicians. The investigators sought 10-15 volunteer physicians from each site (60-90 physicians), and asked them to complete data checklists on 10 consecutive adolescent patients (600-900 visits). After a training session, each site randomly selected data collection periods.

Physicians provided usual care for adolescent patients and recorded on the checklists any prevention discussions during the visit.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date February 2005
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 21 Years to 65 Years
Eligibility Inclusion Criteria:

- Family Medicine Residency physicians and faculty in six residency programs in Texas

Exclusion Criteria:

- Physicians not in the residency programs

Study Design

Allocation: Random Sample, Primary Purpose: Screening, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Locations
Country Name City State
United States Christus Memorial Hospital Spohn Family Medicine Residency Program Corpus Christi Texas
United States Valley Baptist Family Medicine Program Harlingen Texas
United States McAllen Family Medicine Residency Program McAllen Texas
United States Department of Family and Community Medicine UTHSCSA San Antonio Texas
United States Family Medicine Residency Program, Christus Santa Rosa Hospital San Antonio Texas

Sponsors (1)
Lead Sponsor Collaborator
The University of Texas Health Science Center at San Antonio

Country where clinical trial is conducted

United States, 

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