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

Breastfeeding Clinical Trial

Official title:

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

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05993936
• Other study ID #: 129
• Status: Not yet recruiting
• Phase: N/A
• Start date: November 1, 2023
• Est. completion date: September 1, 2024

Study information

• Verified date: August 2023
• Source: Cukurova University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 80
• Est. completion date: September 1, 2024
• Est. primary completion date: September 1, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 35 Years

Eligibility

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

Related Conditions & MeSH terms

• Breastfeeding

Intervention

Device:
• mobile application
A mobile application developed by researchers for the problems experienced in the postpartum period and downloaded from the play store.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Cukurova University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	mobile application aim 1	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
Primary	mobile application aim 2	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]