Psychological Profile of Women With Infertility in Egypt: A Comparative Study

December 21, 2015 updated by: Ahmed Mohamed Bahaa El Din, Ain Shams Maternity Hospital
The aim of this study is to determine the prevalence of psychological affection in infertile egyptian women

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

Comparative cross sectional study

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

20 years to 40 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Sampling Method

Probability Sample

Study Population

This study will be conducted at the department of Obstetrics and Gynecology of Ain shams university and Zagazig university and some private centres for the treatment of infertility. It will include 400 women, divided into two groups (control group and clinical group) starting from January 2016.

Description

Inclusion Criteria:

Control group:

  • Pregnant women.
  • At least one live birth.
  • Age group 20-40 years.

Clinical group:

  • Infertile women either primary or secondary according to (WHO,2013).
  • Age group 20-40ys.
  • Different levels of education.
  • Different methods of treatment of infertility (medical or IVF)
  • Half of them from rural area the other half from urban area.

Exclusion Criteria:

  • Male factor of infertility.
  • The women with psychiatric disorders.
  • The women with physical and medical disorders.
  • The women whose current pregnancy has any problems (e.g. growth retardation, macrosomia, placenta previa, threatened abortion, or preterm labour).
  • The women with history of intrauterine fetal death.

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
determination of the prevalence of depression among infertile women
Time Frame: 6 months
questionnaire will be used to collect qualititiative data from women
6 months

Collaborators and Investigators

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

Sponsor

Ain Shams Maternity Hospital

Investigators

  • Study Director: sherif a akl, professor of obstetric and gynecology

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

January 1, 2016

Primary Completion (Anticipated)

July 1, 2016

Study Completion (Anticipated)

July 1, 2016

Study Registration Dates

First Submitted

December 15, 2015

First Submitted That Met QC Criteria

December 21, 2015

First Posted (Estimate)

December 23, 2015

Study Record Updates

Last Update Posted (Estimate)

December 23, 2015

Last Update Submitted That Met QC Criteria

December 21, 2015

Last Verified

December 1, 2015

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • ADin

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

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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