Importance: Black teenaged women have disproportionately high rates of unintended pregnancy (UTP) and sexually transmitted infections (STI). Internet-based interventions can be delivered to large groups of people in a relatively inexpensive manner. Objective: The purpose of this randomized trial was to examine the efficacy of an adaptation of a theory- and evidence-based UTP/STI prevention intervention for older teens and for internet delivery. Design: A randomized, attention-controlled trial. Setting: Participants were recruited from minority-serving institutions and community events in New Orleans, Louisiana. Participants: Black women aged 18-19 who were not pregnant nor seeking to become pregnant were enrolled (n=637). Main outcomes and measures: Participants were randomized to an 8-session intervention or attention control and were followed at 6- and 12-months post-intervention to determine if the use of reliable contraception, dual methods, intention to use condoms, and intention to use reliable contraception were higher among women in the intervention arm compared to controls. Pregnancy and STI rates were also compared. Results: Overall, at baseline, reliable contraception was 54.8% and dual protection was 29.4% and the prevalence of STI was 11.1%. Participants were similar by arm. Participation and follow-up rates were excellent (60.9% and 80.3%). At 6 months, all outcomes were improved in intervention compared to control, but this effect waned by 12 months. Conclusion and Relevance: The intervention was efficacious for increasing self-reported pregnancy and STI prevention behavior and intentions and lower trends for pregnancy and STIs were observed in this group which decreased over time suggesting the need for a booster.
Competing Interest StatementThe authors have declared no competing interest.
Clinical TrialNCT01579617
Funding StatementThis study was funded by Office of Adolescent Health, U.S. Department of Health & Human Services (HHS)
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
Tulane University Institutional Review Board
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Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines and uploaded the relevant EQUATOR Network research reporting checklist(s) and other pertinent material as supplementary files, if applicable.
Yes
Data AvailabilityData for the present study is unable to be shared
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