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Evaluation of the Effectiveness of the Teen Options to Prevent Pregnancy (T.O.P.P.) Program

Evaluation of the Effectiveness of the Teen Options to Prevent Pregnancy (T.O.P.P.) Program

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01456793
Enrollment
598
Registered
2011-10-21
Start date
2011-10-31
Completion date
2016-09-30
Last updated
2017-03-07

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

Conditions

Pregnancy

Keywords

Pregnancy prevention, Pregnancy, Birth, Contraceptive use, Adolescents

Brief summary

The purpose of this study is to evaluate the effectiveness of the Teen Options to Prevent Pregnancy (T.O.P.P.) program in increasing contraceptive use and reducing repeat pregnancies among pregnant and parenting adolescents in central Ohio.

Detailed description

The risk for teen pregnancy is especially high among teen mothers, leading, in some cases, to unsafe intervals between teen births. The Teen Options to Prevent Pregnancy (T.O.P.P.) program is an 18-month clinic-based program that aims to reduce repeat pregnancies among pregnant and parenting adolescents by providing telephone-based care coordination and mobile contraceptive services to this high-risk population. This study uses a randomized controlled design to compare the effectiveness of T.O.P.P. versus usual care provided to patients at participating clinics. Study participants will be adolescent mothers between the ages of 10 to 19 recruited through seven OhioHealth women's health clinics and three OhioHealth hospitals covering seven counties in central Ohio. This study is being conducted as part of the national Evaluation of Adolescent Pregnancy Prevention Approaches funded by the U.S. Department of Health and Human Services' Office of Adolescent Health.

Interventions

BEHAVIORALTeen Options to Prevent Pregnancy (T.O.P.P.)

Telephone-based care coordination and mobile contraceptive services

Sponsors

OhioHealth Research and Innovation Institute
CollaboratorUNKNOWN
Nationwide Children's Hospital
CollaboratorOTHER
Mathematica Policy Research, Inc.
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
10 Years to 19 Years
Healthy volunteers
No

Inclusion criteria

* 10 - 19 years old * Female * 28 weeks pregnant through 8 week post partum * Medicaid recipient * English speaking * Patient of OhioHealth

Design outcomes

Primary

MeasureTime frame
Incidence of repeat pregnancy30 months after baseline

Secondary

MeasureTime frame
Contraceptive Use6 months after baseline

Countries

United States

Outcome results

None listed

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