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Completed Not applicable Interventional Accepts healthy volunteers

Louisville Teen Pregnancy Prevention Project

ClinicalTrials.gov ID: NCT01411878

Public ClinicalTrials.gov record NCT01411878. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 5:43 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Creating Healthy Adolescents Through Meaningful Prevention Services

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is comparing the impact of two teen pregnancy prevention interventions, Reducing the Risk and Love Note with a non-related training on community building to determine which is most effective for which participants in delaying sexual initiation, enhancing use of condoms and other forms of birth control, decreasing sexually transmitted diseases and decreasing the number of pregnancies. The participants were 1450 youth between the ages of 14 and 19 including those from poor urban settings, those from immigrant and refugee families and those from the foster care system. Both girls and boys were be in the study. The investigators predict that girls, immigrants and refugees and foster youth will have better outcomes when participating in Love Notes, a program focused on healthy relationship formation and maintenance as a frame for how to manage the sexual aspect of relationships while boys and urban youth will have better outcomes when participating in Reducing the Risk. Both groups will have better outcomes than those in the control condition.

Study identification

NCT ID
NCT01411878
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
University of Louisville
Other
Enrollment
1,450 participants

Conditions and interventions

Interventions

Behavioral

Eligibility (public fields only)

Age range
14 Years to 19 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2011
Primary completion
Feb 28, 2014
Completion
Mar 31, 2016
Last update posted
Apr 23, 2017

2011 – 2016

United States locations

U.S. sites
12
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Department for Community Based Services: Jefferson County Region Louisville Kentucky 40203
House of Ruth Louisville Kentucky 40203
Presbyterian Community Center Louisville Kentucky 40203
Jewish Family and Career Services Louisville Kentucky 40205
Gate of Hope Ministries Louisville Kentucky 40207
St George Community Center Louisville Kentucky 40210
Neighborhood House Louisville Kentucky 40212
One Plus One Equals You Louisville Kentucky 40212
Americana Community Center Louisville Kentucky 40214
Canaan Community Development Corporation Louisville Kentucky 40218
Maryhurst Louisville Kentucky 40223
The Steward's Staff Louisville Kentucky 40259

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01411878, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 23, 2017 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01411878 live on ClinicalTrials.gov.

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