THE EFFECT OF E-MOBILE TRAINING GIVEN POSTNATAL PERIOD ON POSTNATAL COMFORT AND BREASTFEEDING SELF-EFFICIENCY

• Sponsor: Cukurova University (Other)
• Overall Status: Not yet recruiting
• CT.gov ID: NCT05993936
• Collaborator: (none)
• Enrollment: 80
• Arms: 2
• Anticipated Duration (Months): 12

Study Details

Study Description

Brief 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.

Condition or Disease	Intervention/Treatment	Phase
Breastfeeding	Device: mobile application	N/A

Study Design

• Study Type: Interventional
• Anticipated Enrollment: 80 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Single (Participant)
• Primary Purpose: Prevention
• Official Title: THE EFFECT OF E-MOBILE TRAINING GIVEN IN THE POSTNATAL PERIOD ON POSTNATAL COMFORT AND BREASTFEEDING SELF-EFFICIENCY
• Anticipated Study Start Date: Sep 1, 2023
• Anticipated Primary Completion Date: Sep 1, 2024
• Anticipated Study Completion Date: Sep 1, 2024

Arms and Interventions

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.	Device: mobile application; 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

Outcome Measures

Primary Outcome Measures

1. mobile application aim 1 [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

2. mobile application aim 2 [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

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 35 Years
• Sexes Eligible for Study: Female
• Accepts Healthy Volunteers: Yes

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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

• Cukurova University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: seda karaçay yıkar, Assistant professor, Cukurova University
• ClinicalTrials.gov Identifier: NCT05993936
• Other Study ID Numbers: 129
• First Posted: Aug 15, 2023
• Last Update Posted: Aug 15, 2023
• Last Verified: Aug 1, 2023

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

Study Results

No Results Posted as of Aug 15, 2023