ClinicalTrials.Veeva

Menu

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

Ç

Çukurova University

Status

Not yet enrolling

Conditions

Breastfeeding

Treatments

Device: mobile application

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

80 estimated patients

Sex

Female

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

80 participants in 2 patient groups

e mobile aplication
Experimental group
Description:
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.
Treatment:
Device: mobile application
control
No Intervention group
Description:
this group will only receive the standard care provided in the hospital. no intervention will be made

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems