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Effect of Biological Nurturing Education to Pregnant Women on Breastfeeding Status

I

Istanbul University - Cerrahpasa (IUC)

Status

Completed

Conditions

Breastfeeding

Treatments

Behavioral: Breastfeeding Education

Study type

Interventional

Funder types

Other

Identifiers

NCT05593536
2022/84

Details and patient eligibility

About

Aim: This study was randomized to determine the effect of biological nurturing education given to nulliparous pregnant women on breastfeeding status.

Method: The population of the study consisted of pregnant women who are visiting Istanbul Training and Research Hospital Suleymaniye Obstetrics and Pediatrics Hospital between October 2022 and August 2023. F test at 90% effect power 0.25 medium effect level on the sample of the study analyzed using the Gpower (3.1.9.2) Programe. As a result of the analyze, it was planned to recruit 207 nulliparous pregnant women. According to the calculation made, there should be at least 69 people in each groups. Accordingly, 69 people in the experimental 1 group (biological nurturing), 69 people in the experimental 2 group (classical breastfeeding), 69 people should be included in the control group. Experimental 1 group and experimental 2 group will be given breastfeeding training on their first visit and after two weeks. Breastfeeding success in the postpartum period will be compared in all groups.

Enrollment

207 patients

Sex

Female

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

GROUP 1:

  • 18-35 age range
  • Nulliparous Pregnancy
  • Single Pregnancy
  • Gestational week 34- 36
  • Those who are literate
  • Those who have a smart phone and have the opportunity to benefit from teaching methods

GROUP 2:

  • 18-35 age range
  • Nulliparous Pregnancy
  • Single Pregnancy
  • Gestational week 34-36
  • Those who are literate

GROUP 3:

  • 18-35 age range
  • Nulliparous Pregnancy
  • Single Pregnancy
  • Gestational week 34-36 gw
  • Those who are literate

Exclusion criteria

GROUP1:

  • Presence of chronic disease
  • Nipple problems
  • Admission of the baby to the neonatal intensive care unit
  • The presence of anomaly related to the baby (chromosomal anomaly, cleft palate/lip, tongue tie)
  • Mothers in whom breastfeeding will be prohibited/suspected in the postpartum period
  • The presence of a disease in the mother that will prevent breastfeeding
  • Pregnant women with vision and hearing problems

GROUP 2:

  • Presence of chronic disease
  • Nipple problems
  • Admission of the baby to the neonatal intensive care unit
  • The presence of anomaly related to the baby (chromosomal anomaly, cleft palate/lip, tongue tie)
  • Mothers in whom breastfeeding will be prohibited/suspected in the postpartum period
  • The presence of a disease in the mother that will prevent breastfeeding
  • Pregnant women with vision and hearing problems

GROUP 3:

  • Pregnant women who go to pregnancy school
  • Presence of chronic disease
  • Nipple problems
  • Admission of the baby to the neonatal intensive care unit
  • The presence of anomaly related to the baby (chromosomal anomaly, cleft palate/lip, tongue tie)
  • Mothers in whom breastfeeding will be prohibited/suspected in the postpartum period
  • The presence of a disease in the mother that will prevent breastfeeding
  • Pregnant women with vision and hearing problems

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

207 participants in 3 patient groups

Group 1 (biological nurturing)
Experimental group
Description:
In biological feeding, the mother takes a semi-sitting position and the baby lies face down on the mother's breast and belly, with every part of her body in contact with the mother.
Treatment:
Behavioral: Breastfeeding Education
Group 2 (classic breastfeeding)
Experimental group
Description:
In classical breastfeeding, the mother holds her baby in her arms and breastfeeds while she is in a sitting position.
Treatment:
Behavioral: Breastfeeding Education
Group 3 (control)
No Intervention group
Description:
The mother will breastfeed her baby as she wishes.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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