- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT00849823
HIV Prevention Program for African American Teen Males
A Brief, Clinic-Based, HIV Prevention Program for African American Teen Males
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Based on the observation that African Americans are vastly more likely than their white and Hispanic counterparts to be infected by the human immunodeficiency virus (HIV), the Centers for Disease Control and Prevention (CDC) has termed AIDS a "health crisis" for African Americans and has called for a heightened national response to this glaring racial disparity. The crisis is especially dramatic in the Southern United States. Thus, the search for effective interventions tailored to this population is a national priority. This study expands upon a previous study conducted among young African American men. In the previous study we developed and tested the efficacy of a brief, clinic-based, program designed to interactively promote safer sex for African American men (18 to 29 years of age) engaging in sex with women. Adjusted findings from the previous study provided relatively robust support for program efficacy, with men who received the intervention program being about two-thirds less likely, than controls, to acquire an STI during a 6-month period. This study expands on the work performed in the previous study by developing and testing a version for younger African American males (i.e., teen males).
The purpose of this study is to test the efficacy of a brief, clinic-based and theory-guided, intervention designed to reduce STI incidence among African American teen (15 to 20 years old) males presenting themselves for STI testing.
Type d'étude
Inscription (Anticipé)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
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Louisiana
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New Orleans, Louisiana, États-Unis, 70118
- Adolescent Medicine Program, LSU School of Medicine
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- at least 15, but not more than 23 years of age
- attending the clinic for the expressed purpose of being tested for sexually transmitted infections
- engaging in penetrative sex (penile-vaginal or penile-anal) at least once in the past 2 months
- willingness to return for the two planned follow-up assessments
Exclusion Criteria:
- self-report of being HIV positive
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: La prévention
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
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Comparateur actif: Male Sexual Health Program
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An attention equivalent control condition entailing a 60-minute one-to-one session that will didactically teach teens about several aspects of male sexual health.
The content and objectives are related only to knowledge acquisition.
In addition to this program, teens randomized to the control condition will receive standard-of-care services from the clinic.
This involves the provision of free condoms (one size "fits all" condoms) and a brief (nurse-delivered) counseling message to practice safer sex.
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Expérimental: Focus on the Future Program
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A 60-minute, theory-guided program designed to increase the quality and frequency of teens' condom use within the context of making safer choices regarding partners and sexual behaviors.
The program is explicitly designed to increase the quality and frequency of teen's condom use.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
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Incidence rate of laboratory-confirmed STIs
Délai: 2- and 6-month follow-up, as well as 12-month follow-up medical records review
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2- and 6-month follow-up, as well as 12-month follow-up medical records review
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Self-report of unprotected penetrative sex (past 30 days)
Délai: 2- and 6-month follow-up
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2- and 6-month follow-up
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Self-report of number of penetrative (penile-vaginal or penile-anal) sex partners (past 30 days)
Délai: 2 and 6-month follow-up
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2 and 6-month follow-up
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Self-report of negative experiences with the correct use of condoms (past 30 days)
Délai: 2- and 6-month follow-up
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2- and 6-month follow-up
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Ryan Pasternak, MD, MPH, Louisiana State University Health Sciences Center in New Orleans
Publications et liens utiles
Publications générales
- Crosby RA, Mena L, Smith RV. Promoting positive condom use experiences among young black MSM: a randomized controlled trial of a brief, clinic-based intervention. Health Educ Res. 2018 Jun 1;33(3):197-204. doi: 10.1093/her/cyy010.
- Crosby RA, Mena L, Salazar LF, Hardin JW, Brown T, Vickers Smith R. Efficacy of a Clinic-Based Safer Sex Program for Human Immunodeficiency Virus-Uninfected and Human Immunodeficiency Virus-Infected Young Black Men Who Have Sex With Men: A Randomized Controlled Trial. Sex Transm Dis. 2018 Mar;45(3):169-176. doi: 10.1097/OLQ.0000000000000721.
- Crosby R, Salazar LF. Reduction of condom use errors from a brief, clinic-based intervention: a secondary analysis of data from a randomised, controlled trial of young black males. Sex Transm Infect. 2015 Mar;91(2):111-5. doi: 10.1136/sextrans-2013-051492. Epub 2014 Jun 4.
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 080666
- NIH Grant # 1R01MH083621
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