Recruitment

Recruitment Status
Completed
Estimated Enrollment
700

Summary

Conditions
  • Pregnancy
  • Sexually Transmitted Infections
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Primary Purpose: Prevention

Participation Requirements

Age
Between 18 years and 19 years
Gender
Only males

Description

The investigators will test the hypothesis that by the end of the study, women who receive the e-SIHLE intervention will have a 35% increase in reliable contraception use compared to attention control website, DIVAS, which is a health and nutrition education program. Both arms of the study were desi...

The investigators will test the hypothesis that by the end of the study, women who receive the e-SIHLE intervention will have a 35% increase in reliable contraception use compared to attention control website, DIVAS, which is a health and nutrition education program. Both arms of the study were designed for African-American women who are 18-19 years old.

Tracking Information

NCT #
NCT01579617
Collaborators
Department of Health and Human Services
Investigators
Principal Investigator: Patricia Kissinger, BSN MPH PhD Tulane University Health Sciences Center, School of Public Health and Tropical Medicine