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Completed No phase listed Observational Accepts healthy volunteers

Creighton Model Effectiveness, Intentions and Behaviors Assessment (CEIBA)

ClinicalTrials.gov ID: NCT01012596

Public ClinicalTrials.gov record NCT01012596. 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 8, 2026, 7:21 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

Effectiveness, Intention, and Behavior in Creighton Model NFP Use

Brief summary

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

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).

Study identification

NCT ID
NCT01012596
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
University of Utah
Other
Enrollment
624 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 40 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
Sep 30, 2009
Primary completion
Sep 30, 2012
Completion
Apr 30, 2013
Last update posted
Feb 22, 2022

2009 – 2013

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Sacramento Diocese FertilityCare Services Sacramento California 95825
Northland Family Programs: A FertilityCare Center Duluth Minnesota 55102
Twin Cities FertilityCare Center Saint Paul Minnesota 55102
FertilityCare Center of Kansas City Blue Springs Missouri 64014
St. John's Mercy Medical Center, Department of FertilityCare Services St Louis Missouri 63141
FertilityCare Center, Diocese of Lincoln Lincoln Nebraska 68501
FertilityCare Center of Omaha Omaha Nebraska 68106
FertilityCare Services St. Joseph Hospital Nashua New Hampshire 03060
St. Joseph FertilityCare Center Albuquerque New Mexico 87120
Caritas FertilityCare Center Pataskala Ohio 43062
Center for Women's Health, Spirit FertilityCare Services Camp Hill Pennsylvania 17011
FertilityCare Services: Diocese of Charleston, SC Greer South Carolina 29650
FertilityCare Center of North Texas Fort Worth Texas 76137
Women's FertilityCare Services of Houston Houston Texas 88018
Intermountain FertilityCare Center Salt Lake City Utah 84106
If you don't find a center near you, contact us for Long Distance Learning Salt Lake City Utah 84112
FertilityCare Center of the Upper Ohio Valley Weirton West Virginia 26062

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01012596, 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 Feb 22, 2022 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01012596 live on ClinicalTrials.gov.

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