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Clinical trialNCT01012596CompletedObservational

Creighton Model Effectiveness, Intentions and Behaviors Assessment (CEIBA)

SponsorUniversity of UtahEnrollment624FertilityPregnancy
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The Creighton Model (CrM) FertilityCare System is a natural family planning method that teaches couples to recognize and chart the signs of fertility and infertility in the woman's cycle and to use that knowledge to either achieve or avoid a pregnancy. The method is natural, safe and effective, and it helps the couple understand their fertility. Trained practitioners at FertilityCare Centers teach the Creighton Model across the country, internationally and long distance. Several FertilityCare Centers and the University of Utah are conducting a study to evaluate the effectiveness of the Creighton Model (CrM) for new and return users wanting to avoid pregnancy. While past studies have shown that the Creighton Model is a highly effective method, this study will use new ways to measure how well it works. This is important because the knowledge gained will improve comparisons between the Creighton Model and other family planning methods. The study will also explore intentions and behaviors of couples to avoid or achieve a pregnancy. The investigators hypothesize that for the CrM the pregnancy rate during perfect use to avoid pregnancy will be about 1% and the behaviorally determined avoiding-related pregnancy rate for the CrM will be about 6%. The investigators will also evaluate the pregnancy rate during "typical use" without a previously stated intention to conceive (in CrM terms, a mixture of avoiding and achieving-related behavior).

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

18 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Canada
  • Marguerite Bourgeoys Fertilitycare Programme

    Toronto, Ontario, Canada

United States
  • Sacramento Diocese Fertilitycare Services

    Sacramento, California, United States

  • Northland Family Programs: A Fertilitycare Center

    Duluth, Minnesota, United States

  • Twin Cities Fertilitycare Center

    Saint Paul, Minnesota, United States

  • Fertilitycare Center of Kansas City

    Blue Springs, Missouri, United States

  • St. John'S Mercy Medical Center, Department of Fertilitycare Services

    St Louis, Missouri, United States

  • Fertilitycare Center, Diocese of Lincoln

    Lincoln, Nebraska, United States

  • Fertilitycare Center of Omaha

    Omaha, Nebraska, United States

  • Fertilitycare Services St. Joseph Hospital

    Nashua, New Hampshire, United States

  • St. Joseph Fertilitycare Center

    Albuquerque, New Mexico, United States

  • Caritas Fertilitycare Center

    Pataskala, Ohio, United States

  • Center for Women'S Health, Spirit Fertilitycare Services

    Camp Hill, Pennsylvania, United States

  • Fertilitycare Services: Diocese of Charleston, Sc

    Greer, South Carolina, United States

  • Fertilitycare Center of North Texas

    Fort Worth, Texas, United States

  • Women'S Fertilitycare Services of Houston

    Houston, Texas, United States

  • If You Don'T Find A Center Near You, Contact Us for Long Distance Learning

    Salt Lake City, Utah, United States

  • Intermountain Fertilitycare Center

    Salt Lake City, Utah, United States

  • Fertilitycare Center of the Upper Ohio Valley

    Weirton, West Virginia, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Oct 2009
Primary completion
31 Oct 2012
Completion
31 May 2013
Last update posted
23 Feb 2022
Registered enrollment
624
Registry id
NCT01012596

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 11 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.