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e-SiHLE: An Internet Pregnancy Prevention for Older Teenage Girls

e-SiHLE: An Internet Pregnancy Prevention for Older Teenage Girls

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01579617
Acronym
eSiHLE
Enrollment
637
Registered
2012-04-18
Start date
2012-08-31
Completion date
2015-12-31
Last updated
2016-12-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy, Sexually Transmitted Infections

Keywords

pregnancy, STI, STD

Brief summary

The purpose of this study is to evaluate the efficacy of an online pregnancy prevention intervention that was adapted from the evidence based small group intervention SiHLE.

Detailed 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 designed for African-American women who are 18-19 years old.

Interventions

BEHAVIORALBUtiful.

8 website sessions include themes that teach: gender empowerment, assertive communication skills, goal setting, pregnancy and STI/HIV risk, safer sex behaviors, proper condom use, positive attitudes and norms towards consistent condom use, contraception, partner involvement in safer sex, and responsibility for their own health.

BEHAVIORALDIVAS.

Attention control arm: 8 website sessions that include topics on: healthy eating, choosing nutritional snacks, sugar and salt intake, physical activity, stress management, foods for beauty.

Sponsors

Department of Health and Human Services
CollaboratorFED
Tulane University Health Sciences Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 19 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 18 or 19 at enrollment * Female * Not currently pregnant or intending to become pregnant in the next 12 months * Live in Orleans or Jefferson Parish in Louisiana * English is your primary language * Access to a computer and internet connection * Does not have sex with women exclusively

Exclusion criteria

* Age younger than 18 or older than 19 * Male * Currently pregnant or intend to become pregnant in the next 12 months * Live outside of Orleans or Jefferson Parish * Hearing impairments that prevent listening to videos

Design outcomes

Primary

MeasureTime frameDescription
Percent change from baseline in the use of reliable contraceptivesChange from baseline measured at 3 and 7 and 13 months post baselineWomen who receive the BUtiful intervention will have a 35% increase in the use of reliable contraceptives compared to the DIVAS intervention. Reliable contraceptive use is defined as the consistent use of a condom with all sex partners, a hormonal birth control method, or an intrauterine device.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026