The Safe Teen Study
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Purpose
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.
| Condition |
|---|
|
Prevention |
| Study Type: | Observational |
| Study Design: | Allocation: Random Sample Primary Purpose: Screening Time Perspective: Cross-Sectional Time Perspective: Prospective |
| Official Title: | The SAFE TEEN Study: Family Physicians' Reports of Facilitators of and Barriers to Preventive Care for Adolescents. |
| Estimated Enrollment: | 60 |
| Study Start Date: | June 2004 |
| Estimated Study Completion Date: | February 2005 |
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.
Eligibility| Ages Eligible for Study: | 21 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Family Medicine Residency physicians and faculty in six residency programs in Texas
Exclusion Criteria:
- Physicians not in the residency programs
Contacts and Locations| 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 | |
| Department of Family and Community Medicine UTHSCSA | |
| San Antonio, Texas, United States, 78229 | |
| Family Medicine Residency Program, Christus Santa Rosa Hospital | |
| San Antonio, Texas, United States, 78207 | |
| Principal Investigator: | Sandra K Burge, Ph.D. | University of TexasHealth Science Center at San Antonio |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00380510 History of Changes |
| Other Study ID Numbers: | HP000016-02 |
| Study First Received: | September 25, 2006 |
| Last Updated: | September 25, 2006 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by The University of Texas Health Science Center at San Antonio:
|
Family Physicians Adolescents Preventive Care Health Behavior |
ClinicalTrials.gov processed this record on May 16, 2013