The Effect Of E-Mobıle Traınıng Gıven Postnatal Perıod On Postnatal Comfort And Breastfeedıng Self-Effıcıency

September 22, 2023 updated by: seda karaçay yıkar, Cukurova University

The Effect Of E-Mobıle Traınıng Gıven In The Postnatal Perıod On Postnatal Comfort And Breastfeedıng Self-Effıcıency

The period until the 42nd day after birth is called the postpartum period by the World Health Organization (WHO) Especially the first week of the postpartum period is the transition period both physiologically and psychologically, and the period when postpartum problems are at the highest level.This study was planned as a two-group control and e-mobile application in order to determine the effect of e-mobile training given in the postpartum period on postpartum comfort and breastfeeding self-efficacy.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

80

Phase

  • Not Applicable

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:

The ages of 18-35, Primiparous and multiparous pregnancy, Not clinical diagnosis of risky pregnancy, Able to understand and speak Turkish, Without communication difficulties and mental disabilities The mother and the baby have not developed any complications during pregnancy, delivery and postpartum period, Having a smart phone in the mobile application group, Those who have not attended childbirth preparation classes,

Exclusion Criteria:

  • Preterm birth
  • Postterm birth

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: e mobile aplication
Postpartum period mobile application; It is an application that is prepared according to the Android Operating System, can be downloaded free of charge from the Google Play Store, and offers training and live counseling services for women who have given birth.
A mobile application developed by researchers for the problems experienced in the postpartum period and downloaded from the play store.
No Intervention: control
this group will only receive the standard care provided in the hospital. no intervention will be made

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
mobile application aim 1
Time Frame: postpartum 7th week
Thanks to the mobile application, it is planned to develop women's breastfeeding self-efficacy. As the scale score increases, self-efficacy changes
postpartum 7th week
mobile application aim 2
Time Frame: postpartum 7th week]
Thanks to the mobile application, it is expected that the postpartum comfort of women will changes. As the score obtained from the scale increases, the comfort changes
postpartum 7th week]

Collaborators and Investigators

This is where you will find people and organizations involved with this 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 (Estimated)

November 1, 2023

Primary Completion (Estimated)

September 1, 2024

Study Completion (Estimated)

September 1, 2024

Study Registration Dates

First Submitted

July 18, 2023

First Submitted That Met QC Criteria

August 14, 2023

First Posted (Actual)

August 15, 2023

Study Record Updates

Last Update Posted (Actual)

September 26, 2023

Last Update Submitted That Met QC Criteria

September 22, 2023

Last Verified

August 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 129

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 Breastfeeding

Clinical Trials on mobile application

Subscribe