Clinical Trials Directory

Trials / Completed

CompletedNCT00843336

Comparison of Two Internet Supported Natural Family Planning Methods

Randomized Comparison of Two Internet Supported Natural Family Planning Methods

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
358 (actual)
Sponsor
Marquette University · Academic / Other
Sex
All
Age
18 Years – 42 Years
Healthy volunteers
Accepted

Summary

The purpose of this research study is to compare the effectiveness of two natural family planning (NFP) methods that are provided over the internet by the Marquette University Institute for Natural Family Planning. One of the NFP methods is the use of a hand held electronic hormonal fertility monitor. The other method involves the self-observation of cervical mucus to track fertility. Both of the methods will involve placing information about fertility into an online charting system that automatically displays the days of fertility and infertility. The investigators are also interested in the influence of mutual motivation by the woman and her partner in using these methods to avoid pregnancy. The investigators hypothesize that there will be lower unintended pregnancy rates among those couples who use the electronic hormonal fertility monitor and among those couples who have a strong motivation to avoid pregnancy.

Detailed description

The Office of Population Affairs (OPA) of the Department of Human Development recently submitted a call for proposals for research on methods of natural family planning (NFP). The department chairs of OPA have recognized that relatively few women in the United States use natural methods of family planning, especially in the Title X Family Planning programs and clinics. They wanted researchers to develop studies to help increase the use and the efficacy of these methods, and, furthermore, wanted to understand why the methods are not used more. Reasons why only about 0.2% of US women use natural methods of birth control are they are often difficult to use, they are relatively ineffective, and there is a lack of access to properly trained NFP teachers. At Marquette University we have developed simple methods of NFP that utilize an electronic fertility monitor that measures female reproductive hormones, self cervical mucus monitoring that estimates the fertile window, and a simple fertility formula to help estimate the beginning and end of the fertile window. We also have developed a Web site that offers easy access to information on NFP, electronic charting, and professional nurses with specialization in teaching NFP. The specific purpose of our study is to determine the efficacy, satisfaction, ease of use, and motivation in using an internet based NFP method that utilizes an electronic hormonal fertility monitor plus a simple fertility formula (i.e., EHFM-NFP) within an online professional-nurse supported system. Since there are few studies that compare methods of NFP, another aim of this study is to compare an internet based EFHM-NFP method with an internet based traditional cervical mucus monitoring (CMM) NFP method - both methods were developed at Marquette University. Please note that we have 3 published efficacy studies of the Marquette Method. The specific research questions that will be asked are: 1. What are the 3, 6, and 12-month unintended pregnancy rates of an internet-provided EHFM-aided NFP method? 2. What are the 3, 6, and 12-month unintended pregnancy rates of an internet-provided CMM-only NFP method? 3. What is the satisfaction, ease of use, and mutual motivation of an internet-based NFP method (either EFHM or CMM) over a 12-month time period, i.e., after 1, 3, 6, and 12 months of use?

Conditions

Interventions

TypeNameDescription
BEHAVIORALElectronic hormonal fertility monitoringUse of an electronic hormonal fertility monitor that provides three levels of fertility; low, high, and peak. Monitor is based upon urinary levels of E3G (estrogen) and LH. Monitor readings are placed in an electronic charting system on the Internet.
BEHAVIORALSelf-monitoringSelf-monitoring of externally observed cervical mucus to determine level of fertility.

Timeline

Start date
2009-02-01
Primary completion
2012-12-01
Completion
2013-12-01
First posted
2009-02-13
Last updated
2015-09-24

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00843336. Inclusion in this directory is not an endorsement.