Division of Clinical Research at Washington University
St Louis, Missouri, 63108, United States
NCT Number: NCT02633631
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.
Looking for future studies?
Notify Me14 year–45 year
Female
Observational
St Louis, Missouri, 63108, United States
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 24 months
Reduce unintended pregnancy by 10% - # of pregnancies that are unintended per 1000 reproductive-age women (14-45 years)
Time frame: 24 months
Reduce unintended births and associated costs by 15% - # of births that are unintended per 1000 reproductive age women
Washington University School of Medicine
Other
The Center for Contraceptive Excellence: an Innovative Health Services Delivery and Payment Model
Acronym: C3
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06320964
Acceptability, Family Planning
Udaipur, Rajasthan, India
View Trial DetailsNCT03534401
Family Planning, Intimate Partner Violence (IPV)
San Diego, California, United States
View Trial DetailsNCT03660514
Family Planning, Intimate Partner Violence (IPV)
La Jolla, California, United States
View Trial DetailsNCT02364037
Contraception, Unintended Pregnancy
St Louis, Missouri, United States
View Trial Details