Contraceptive Choice Center

Completed

• Conditions: Contraception; Unintended Pregnancy; Family Planning

• Registration Number: NCT02633631
• Lead Sponsor: Washington University School of Medicine

Brief Summary

The Contraceptive Choice Center will use an innovative-model of contraceptive care which was developed as a part of the Contraceptive CHOICE Project (CHOICE). This delivery model will deliver high-quality family planning services for women and reduce unintended pregnancies and births. This intervention will result in improved health for women, improved health care, and reduced costs to Medicaid.

The Center will provide care to women ages 14-45 years of age.

Detailed Description

The Center will provide high-quality contraceptive care using the innovative model of the Contraceptive CHOICE Project. Specifically, the model will provide the following components: 1) Structured, evidence-based contraceptive counseling; 2) education of providers about long-acting reversible contraceptive (LARC) methods and evidence-based guidelines for contraceptive provision; 3) removal of patient barriers to family planning services; and 4) post-visit contraceptive support. The model addresses the barriers to contraceptive uptake.

Study Timeline

• Study Start: 2015-01
• Study First Submitted: 2015-04-22
• Study First Submitted QC: 2015-12-14
• Study First Posted: 2015-12-17
• Primary Completion: 2020-04
• Study Completion: 2020-04
• Status Verified: 2021-06
• Last Update Submitted: 2021-06-01
• Last Update Posted: 2021-06-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 2664

Inclusion Criteria

• Childbearing-age seeking family planning services
• Negative pregnancy test
• Willing and able to undergo informed consent

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Exclusion Criteria

• Current participation in a research study that would interfere with the conduct of this study
• Currently pregnant

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Rate of unintended pregnancy	24 months	Reduce unintended pregnancy by 10% - # of pregnancies that are unintended per 1000 reproductive-age women (14-45 years)

Secondary Outcome Measures

Name	Time	Method
Rate of unintended births	24 months	Reduce unintended births and associated costs by 15% - # of births that are unintended per 1000 reproductive age women

Trial Locations

Locations (1)

Division of Clinical Research at Washington University; 🇺🇸 Saint Louis, Missouri, United States