- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00380510
The Safe Teen Study
The SAFE TEEN Study: Family Physicians' Reports of Facilitators of and Barriers to Preventive Care for Adolescents.
Study Overview
Status
Conditions
Detailed 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.
Study Type
Enrollment
Contacts and Locations
Study Locations
-
-
Texas
-
Corpus Christi, Texas, United States, 78405
- Christus Memorial Hospital Spohn Family Medicine Residency Program
-
Harlingen, Texas, United States, 78550
- Valley Baptist Family Medicine Program
-
McAllen, Texas, United States, 78503
- McAllen Family Medicine Residency Program
-
San Antonio, Texas, United States, 78207
- Family Medicine Residency Program, Christus Santa Rosa Hospital
-
San Antonio, Texas, United States, 78229
- Department of Family and Community Medicine UTHSCSA
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Family Medicine Residency physicians and faculty in six residency programs in Texas
Exclusion Criteria:
- Physicians not in the residency programs
Study Plan
How is the study designed?
Design Details
Collaborators and Investigators
Investigators
- Principal Investigator: Sandra K Burge, Ph.D., University of TexasHealth Science Center at San Antonio
Study record dates
Study Major Dates
Study Start
Study Completion
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- HP000016-02
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Prevention
-
Children's Hospital of PhiladelphiaUniversity of Pennsylvania; National Institute of Nursing Research (NINR); Pennsylvania...CompletedPrevention Harmful Effects | Accidents, Traffic | Accident PreventionUnited States
-
Prof Mags BeksinskaCompletedHIV Prevention | Pregnancy PreventionSouth Africa
-
Yale UniversityCompletedHIV Prevention | STI PreventionUnited States
-
Centers for Disease Control and PreventionUniversity of Minnesota; The Fenway Institute; AIDS Action Committee of Massachusetts and other collaboratorsCompletedHIV Prevention | STD PreventionUnited States
-
Children's Hospital Medical Center, CincinnatiCompletedPreventionUnited States
-
Brown UniversityUniversity of California, Los Angeles; National Institute of Nursing Research... and other collaboratorsRecruiting
-
Apple Inc.American Heart AssociationRecruiting
-
Brown UniversityThe Miriam HospitalCompletedOptimizing PrEP Uptake & Adherence Among Male Sex Workers (MSW) Using a 2-stage Randomization DesignPreventionUnited States
-
King Abdulaziz UniversityUnknown