N/A
N=662
Efficacy of an Abstinence-Only HIV Risk-Reduction Intervention for Young African-American Adolescents
HIV Infections · Sexually Transmitted Diseases
Bottom Line
View on ClinicalTrials.gov: NCT00640653 ↗Enrolled (actual)
662
Serious AEs
0.0%
Results posted
Dec 2017
Primary outcome: Primary: Self-report of Ever Having Sexual Intercourse — 39; 40; 44; 31 Participants — p=.03
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Abstinence-only HIV/STD risk-reduction intervention (Behavioral); Safer-sex-only HIV/STD risk-reduction intervention (Behavioral); Long comprehensive HIV/STD risk-reduction intervention (Behavioral); Short comprehensive HIV/STD risk-reduction intervention (Behavioral); Health promotion control intervention (Behavioral)
- Age
- Pediatric, Adult, Older Adult
- Sex
- All
- Sponsor
- University of Pennsylvania
- Primary completion
- Aug 2004
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Self-report of Ever Having Sexual Intercourse |
39; 40; 44; 31; 41 | .03 sig |
| SECONDARY Self-reported Sexual Intercourse in the Past 3 Months |
14; 13; 15; 16; 18; 12 | — |
| SECONDARY Self-report of Having Multiple Sexual Partners in the Past 3 Months |
11; 9; 6; 4; 10; 7 | — |
| SECONDARY Self-reported Consistent Condom Use in the Past 3 Months |
7; 8; 4; 10; 12; 8 | — |
| SECONDARY Self-report of Having Sexual Intercourse Without Using a Condom During the Past 3 Months |
3; 2; 7; 1; 5; 5 | — |
Summary
This study will develop and evaluate the effectiveness of culturally appropriate HIV/sexually transmitted disease risk-reduction interventions in reducing sexual risk behavior among young African-American adolescents.
Eligibility Criteria
Inclusion Criteria
- Grade 6 or 7 student at a participating school
- Written parent or guardian consent to participate
- Self-identifies as African American or black
Exclusion Criteria
- Those not meeting inclusion criteria were excluded.
Data sourced from ClinicalTrials.gov (NCT00640653). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.