Prevalence of Female Circumcision Among Young Women in Beni-Suef, Egypt (FC)

December 18, 2017 updated by: Nesreen Abdel Fattah Abdullah Shehata, Beni-Suef University

Prevalence of Female Circumcision Among Young Women in Beni-Suef, Egypt. A Cross-sectional Study

Female circumcision (FC) is a deeply-rooted practice in Egypt with deblitating physical and psychological consequences, however the previous two decades witnessed sincere efforts to counterfight this practice. The objective of this study is to investigate the prevalence of circumcision among young women (12-25 years) in Beni-Suef , Egypt.

Study Overview

Status

Completed

Conditions

Detailed Description

This cross-sectional study was conducted on a total of 3353young women residing urban and rural quraters in Beni-Suef City. Data was collected usinga questionnaire that included information about the socio-demographic charcteristics of the women, their gynecological data, exposure to FC, and complaints associated with menses during the previous year.

Study Type

Observational

Enrollment (Actual)

3353

Contacts and Locations

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

Study Locations

      • Cairo, Egypt, 018
        • Beni-Suef University

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

12 years to 25 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Probability Sample

Study Population

The urban Metropolitan of Beni-Suef City was classified according to the socioeconomic level of its quarters to low, middle, and high levels. Out of each level, one quarter was selected randomly, by a card withdrawal, where households residing these quarters were chosen using a random start. For the rural villages surrounding the urban Metropolitan, three villages were selected randomly; one on the road to the North, one on the road to the West, and the last one on the road to the South. Each village was clustered roughly into two sites; one to the East of the water channel and one to the West of the same water channel.

In both urban and rural areas, a trained team of data collectors visited the selected households. Householders were informed briefly of the study and the residing women aged between 12 and 25 years were invited to participate and then interviewed.

Description

Inclusion Criteria:

  • Young women aged 12 to 25 years living in Beni-Suef city of Egypt. the urban Metropolitan of Beni-Suef City was classified according to the socioeconomic level of its quarters to low, middle, and high levels. Out of each level, one quarter was selected randomly, by a card withdrawal, where households residing these quarters were chosen using a random start. For the rural villages surrounding the urban Metropolitan, three villages were selected randomly; one on the road to the North, one on the road to the West, and the last one on the road tothe South. Each village was clustered roughly into two sites; one to the East of the water channel and one to the West of the same water channel

Exclusion Criteria:

  • Women from other places in Egypt.

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
Gynecological manifestations measured by a questionnaire.
Time Frame: one year
A questionnaire included questions about the manifestations associated with menses and average duration of dysmenorrhea during the previous year.
one year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
social status measured by a questionnaire
Time Frame: one year
A questionnaire included questions about age at menarche, social, educational and work status.
one year

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
working status measured by a questionnaire
Time Frame: One year
For data collection, a questionnaireof two sections was prepared;the first section included socio-demographic data, social status, working status and educational level,age at menarche, menstrual cycle duration and flow days, in addition to exposure to circumcision. The second section includedquestions about the manifestations associated with menses and average duration of dysmenorrhea
One year

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.

General Publications

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 (Actual)

April 3, 2017

Primary Completion (Actual)

July 15, 2017

Study Completion (Actual)

July 15, 2017

Study Registration Dates

First Submitted

December 8, 2017

First Submitted That Met QC Criteria

December 18, 2017

First Posted (Actual)

December 22, 2017

Study Record Updates

Last Update Posted (Actual)

December 22, 2017

Last Update Submitted That Met QC Criteria

December 18, 2017

Last Verified

December 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • Beni-Suef 14

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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