Skip to main content
Clinical Trials/NCT06268028
NCT06268028
Completed
N/A

The Effect on the Level of Readiness for Discharge of Discharge Training Given to Primiparous Mothers Having a Cesarean Delivery : A Randomized Controlled Study

Aydin Adnan Menderes University1 site in 1 country70 target enrollmentJanuary 10, 2024
ConditionsTraining

Overview

Phase
N/A
Intervention
Not specified
Conditions
Training
Sponsor
Aydin Adnan Menderes University
Enrollment
70
Locations
1
Primary Endpoint
A pre-test applied to 70 women who constitute the sample of the research.
Status
Completed
Last Updated
last year

Overview

Brief Summary

This study aimed to determine the effect of discharge training given to primiparous mothers who gave birth by cesarean section on the level of readiness for discharge.

The research is a pre-test-post-test, randomized controlled experimental study.

Detailed Description

The research is a pre-test-post-test, randomized controlled experimental study. To prevent selection bias, participants were included in the training and control groups by applying the randomization method. The sample consisted of a total of 70 women (experimental group: 35 women and control group: 35 women). The study was carried out with women who lying to Obstetrics Clinic of Aydın Gynecology and Children's Diseases Hospital and met the study criteria.

Registry
clinicaltrials.gov
Start Date
January 10, 2024
End Date
April 30, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Aydin Adnan Menderes University
Responsible Party
Principal Investigator
Principal Investigator

Belma Toptas Acar

Research Assistant Doctor

Aydin Adnan Menderes University

Eligibility Criteria

Inclusion Criteria

  • Able to speak and understand Turkish,
  • At least primary school graduate,
  • 18 years and over,
  • Those who gave birth by cesarean section,
  • Primiparous mothers will be included in the research.

Exclusion Criteria

  • Those who have a physical disability (vision, hearing, etc.) that prevents them from taking care of themselves,
  • In a risky postpartum period,
  • Having a history of chronic disease,
  • Those who were hospitalized during pregnancy,
  • Those who do not have their baby with them after birth,
  • Foreign nationals,
  • Mothers with psychiatric diagnoses will not be included in the study.

Outcomes

Primary Outcomes

A pre-test applied to 70 women who constitute the sample of the research.

Time Frame: 16 weeks

In the pre-test; The individual introduction form and scale used, and the same scale used for the post-test. Individual Introduction Form: Sociodemographic (Age, educational status, health insurance, etc.) and obstetric characteristics (number of pregnancies, number of miscarriages/abortions etc). (15 questions) (RHD-NMF): Scale that evaluates readiness for hospital discharge according to the mother's perception; It consists of four subscales and a total of 23 items. The lowest score that can be obtained from the scale is '0' and the highest score is '220'.

Secondary Outcomes

  • Apost-test applied to 70 women who constitute the sample of the research.(16 weeks)

Study Sites (1)

Loading locations...

Similar Trials