Awareness & Use of Emergency Contraception

November 20, 2019 updated by: Marian Agaiby Ashem, Assiut University

Awareness & Use of Emergency Contraception Among Women Attending Kidwany MCH Center , Assiut City

General objective:

To decrease the percentage of unwanted and/or unplanned pregnancies and their consequences on women's reproductive health.

Specific objectives:

  1. To assess awareness of the study participants about emergency contraception.
  2. Determine the percentage of ever use among the participants.
  3. To identify factors that affect the awareness and use of emergency contraception among the study participants

Study Overview

Status

Unknown

Study Type

Observational

Enrollment (Anticipated)

400

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

15 years to 45 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Married women in reproductive age (15 - 49 years) clients who are attending Kidwany MCH centre, Assiut city.

Description

Inclusion Criteria:

  • Married women in reproductive age (15 - 49 years)

Exclusion Criteria:

  • Infertile and postmenopausal women.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Percent of awareness and use of emergency contraception
Time Frame: baseline
when to use emergency contraception to prevent the unwanted pregnancy
baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

December 1, 2019

Primary Completion (Anticipated)

December 1, 2020

Study Completion (Anticipated)

January 1, 2021

Study Registration Dates

First Submitted

November 19, 2019

First Submitted That Met QC Criteria

November 20, 2019

First Posted (Actual)

November 21, 2019

Study Record Updates

Last Update Posted (Actual)

November 21, 2019

Last Update Submitted That Met QC Criteria

November 20, 2019

Last Verified

November 1, 2019

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Emergency contraception.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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