An Educational HIV Pre-Test Counseling Video Program for Off Hours Testing in the ED: A Randomized Control Trial
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Purpose
This study compared the educational effectiveness of a ten-minute pre-test counseling video with the usual practice of a session with an HIV counselor.
| Condition | Intervention |
|---|---|
|
HIV Counseling and Testing HIV Infections |
Procedure: Educational video |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Bio-equivalence Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Educational/Counseling/Training |
| Official Title: | An Educational HIV Pre-Test Counseling Video Program for Off Hours Testing in the ED: A Randomized Control Trial |
- Comparison of mean knowledge score in both groups.
| Estimated Enrollment: | 130 |
| Study Start Date: | June 2003 |
| Estimated Study Completion Date: | August 2003 |
HIV is increasingly affecting urban populations, making the inner city ED a prime venue for C&T because of their unique opportunity to identify HIV positive patients. These underserved communities often use the ED for their regular health care specifically because it provides services outside of the usual weekday working hours. However, there are significant barriers to HIV C&T in the ED, such as the lack of resources to provide prevention oriented messages, cost issues, and the feasibility of providing the required manpower for testing. The objective of this study is to determine whether an educational video, with the required pre-test counseling elements, conveys the necessary information for inner city ED patients to consent to a standard Elisa HIV test.
In order to address the HIV testing needs of the patient population presenting to the ED, innovative methods must be developed to provide HIV C&T, while simultaneously removing the barriers to testing. Video technology may provide an opportunity to make HIV counseling feasible when counselors are not available.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- All patients awaiting UC treatment were approached for the study.
- Patients 18 years of age and older were included
- Patients who spoke English and Spanish were included.
Exclusion Criteria:
- Clinically unstable,
- Diagnosed with HIV
- Unable to understand the consent process because such patients require unique arrangements for consenting processes.
Contacts and Locations| United States, New York | |
| Jacobi Medical Center | |
| Bronx, New York, United States, 10461 | |
| Principal Investigator: | Yvette Calderon, MD, MS | Jacobi Medical Center, Albert Einstein College of Medicine |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00218907 History of Changes |
| Other Study ID Numbers: | 03-073 |
| Study First Received: | September 19, 2005 |
| Last Updated: | October 21, 2005 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by North Bronx Healthcare Network:
|
HIV prevention HIV counseling HIV testing Emergency Medicine HIV Seronegativity |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases |
Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases |
ClinicalTrials.gov processed this record on May 16, 2013