The Safe Teen Study
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00380510|
Recruitment Status : Completed
First Posted : September 26, 2006
Last Update Posted : September 26, 2006
|Condition or disease|
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 :||Observational|
|Enrollment :||60 participants|
|Official Title:||The SAFE TEEN Study: Family Physicians' Reports of Facilitators of and Barriers to Preventive Care for Adolescents.|
|Study Start Date :||June 2004|
|Study Completion Date :||February 2005|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00380510
|United States, Texas|
|Christus Memorial Hospital Spohn Family Medicine Residency Program|
|Corpus Christi, Texas, United States, 78405|
|Valley Baptist Family Medicine Program|
|Harlingen, Texas, United States, 78550|
|McAllen Family Medicine Residency Program|
|McAllen, Texas, United States, 78503|
|Family Medicine Residency Program, Christus Santa Rosa Hospital|
|San Antonio, Texas, United States, 78207|
|Department of Family and Community Medicine UTHSCSA|
|San Antonio, Texas, United States, 78229|
|Principal Investigator:||Sandra K Burge, Ph.D.||University of TexasHealth Science Center at San Antonio|