Breastfeeding Education Prepared With Virtual Reality Technology

T

TC Erciyes University

Status

Enrolling

Conditions

Breast Feeding

Treatments

Other: virtual reality glasses

Study type

Interventional

Funder types

Other

Identifiers

NCT06229574
ErciyesU-SBF-IT-01

Details and patient eligibility

About

The breastfeeding software developed with the primiparous study was transferred to virtual reality glasses. This study will be applied to pregnant women and its effect on breastfeeding success and breastfeeding self-efficacy will be investigated.

Full description

The goal of this clinical trial is to To learn The Effect Of Pre-Natal Breastfeeding Education Prepared Wıth Virtual Reality Technology On The Breastfeeding Self-Efficiency And Breastfeeding Success Of Primiparous Mothers in The study will be delivered to 60 healthy primiparous pregnant women.The breastfeeding software developed with the primary study was transferred to virtual reality glasses. It will also be implemented in this study. The main questions it aims to answer are: Prenatal breastfeeding education prepared with virtual reality technology positively affects the breastfeeding self-efficacy of primiparous mothers. Prenatal breastfeeding education prepared with virtual reality technology positively affects the breastfeeding of primiparous mothers. Participants will Pregnant women in the intervention group will be given breastfeeding training prepared with virtual reality technology and will fill out questionnaires and scales will be filled in on the first and seventh days after birth. Questionnaires will be filled in by pregnant women in the control group, and the scales will be filled out only on the first and seventh days. Researchers will compare breastfeeding education given with virtual reality glasses with the control group to see whether it has an effect on breastfeeding success and breastfeeding self-efficacy.

Enrollment

60 estimated patients

Sex

Female

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Between the ages of 18 and 35
  • literate,
  • Pregnant women who are at 37 weeks of gestation and above,
  • Those with healthy pregnancies (singleton pregnancy, no systemic/chronic disease, etc.) -Primiparous pregnant women-
  • Vaginal birth planned,
  • planning to breastfeed,
  • Those who do not have any problems with their breasts that would make breastfeeding difficult (collapsed, missing tip, wound on the nipple, etc.),
  • Pregnant women who do not have vision, hearing or communication problems
  • Pregnant women who do not have any problems will be included in the study.

Exclusion criteria

  • Occurrence of a situation that prevents sucking
  • Baby with congenital anomalies

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

intervention group
Experimental group
Description:
The effect of breastfeeding education given with virtual reality glasses on breastfeeding success and breastfeeding self-efficacy will be evaluated. The education given during pregnancy will be evaluated on the first and seventh days after birth.
Treatment:
Other: virtual reality glasses
control group
No Intervention group
Description:
Breastfeeding success and breastfeeding self-efficacy of women included in this group during pregnancy will be evaluated on the first and seventh days after birth.

Trial contacts and locations

1

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Central trial contact

ipek turhan, master; mürüvveet başer, prof.dr

Data sourced from clinicaltrials.gov

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