Effect of Targeted Health Education Program on Nurses' Awareness About Postpartum Depression (PPD)

May 16, 2024 updated by: Rasha Saad, Ain Shams University
To assess nurses' knowledge of PPD at Ain Shams University Maternity Hospital and measure their knowledge level after an educational program on postpartum depression.

Study Overview

Detailed Description

Postpartum depression (PPD) is a serious mental illness that involves the brain and affects behavior and physical health of women after childbirth . Multiple factors may influence PPD, such as lack of support, interpersonal events, withdrawal of hormones after delivery, psychosocial stressors, psychological stressors, personality, environment, and ineffective adaptation.

Symptoms of PPD may include feeling restless or moody, feeling sad, crying a lot, having thoughts about hurting the baby or yourself, not feeling connected to the baby, having no energy or motivation, eating, or sleeping too little or too much, feeling worthless and guilty, losing interest or pleasure in activities, and withdrawing from friends and family .

PPD is one of the most important health problems due to its prevalence; 10-15% . and serious negative mother-baby outcomes. PPD affects the health of mothers and their newborns and is associated with long-term psychological and socioeconomic implications .

As the knowledge affects attitudes and practices of people, nurses' knowledge can affect profoundly women after birth specially regarding PPD .

In an American web-based study , nurses' self-efficacy about PPD was associated to their knowledge . In another American electronic survey of 372 nurses, 95% reported an association between post-partum education and mortality and 72% reported that it is their responsibility to provide education to mothers .

In a Ghanaian study, nurses had good knowledge about PPD but poor knowledge about screening and management . In a Kazakh study, 90% of nurses didn't attend training courses on PPD ).

Furthermore, in a Malaysian study, 44.4 % of participants were below than median total knowledge score and only 25.9% practiced screening. In a Saudi study, the confidence of nurses and midwives to educate women about PPD was associated with their knowledge. In a Turkish study, 84.4 % of nurses had little knowledge and 75.5% reported that psychological service for evaluating mothers wasn't offered.

PPD can have devastating effects on women, their infants, and families associated with lower levels of bonding and reduced breastfeeding initiation and duration. Consequently, women experiencing PPD may cause harm to their baby, themselves, or others.

As, nurses in Maternity Hospitals are poised to play a pivotal role in the early identification and prompt treatment of PPD, assessing their knowledge is very important. To date, according to our knowledge, there is no previous study in Egypt assessing the nurses' knowledge about PPD, therefore the present study will be conducted to compare their knowledge regarding PPD before and after the health education program.

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

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, 1181
        • faculty of medicine Ain shams 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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Nurses at Ain Shams University Maternity Hospital

Exclusion Criteria:

none

-

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

  • Primary Purpose: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: An intervention study (a quasi-experimental design)
An intervention study (a quasi-experimental design)pre&post
Quazi-Experimental study (pre/post design) to assess the Effect of Targeted Health Education Program on Nurses' Awareness About Postpartum Depression
Other Names:
  • Quazi-Experimental study (pre/post design).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To measure the mean change in the nurses' knowledge score after applying the health education program about postpartum depression
Time Frame: one month
Evaluate the effect of the targeted health education program on nurses' knowledge score using a self-administer questionnaire consisting of 28 items covering main issues regarding prevalence risk factors, symptoms, and treatment of PPD. The answer to each question had two options (true or false). The total score ranges from 0-28
one month

Collaborators and Investigators

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

Investigators

  • Principal Investigator: rasha saad Hussein, MD, Faculty of medicine Ain shams univrsity

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)

February 28, 2024

Primary Completion (Actual)

March 28, 2024

Study Completion (Actual)

March 28, 2024

Study Registration Dates

First Submitted

May 10, 2024

First Submitted That Met QC Criteria

May 16, 2024

First Posted (Actual)

May 22, 2024

Study Record Updates

Last Update Posted (Actual)

May 22, 2024

Last Update Submitted That Met QC Criteria

May 16, 2024

Last Verified

May 1, 2024

More Information

Terms related to this study

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.

Clinical Trials on Postpartum Depression

Clinical Trials on Effect of Targeted Health Education Program on Nurses' Awareness About Postpartum Depression

3
Subscribe