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Biological Nutrition Technique Which is Used in Initiation of Breastfeeding (BNTPBSS)

H

Hatice Gul OZTAS

Status

Completed

Conditions

Self Efficacy
Breast Feeding

Treatments

Other: Biological Nutrition Technique

Study type

Interventional

Funder types

Other

Identifiers

NCT05342831
KSUHATİCEGULOZTAS001

Details and patient eligibility

About

Aim: This research was conducted with the purpose of determining the effect of biological nurturing technique used for starting breastfeeding in primipara on breastfeeding success and self-efficacy.

Material and Method: This randomized controlled study was conducted with 130 mothers who had a cesarean section in a public hospital located in Southeast Turkey (65 experimental, 65 control).

Full description

Aim: This research was conducted with the purpose of determining the effect of biological nurturing technique used for starting breastfeeding in primipara on breastfeeding success and self-efficacy.

Material and Method: This randomized controlled study was conducted with 130 mothers who had a cesarean section in a public hospital located in Southeast Turkey (65 experimental, 65 control). The mothers in the control group received routine hospital care. The mothers in the experimental group were taught the biological nurturing technique after the first breastfeeding and breastfeeding was provided according to the technique during the hospitalization. Pre-test data were obtained by applying LATCH and BSES-SF to the mothers in the experimental and control groups at the 1st hour after the first breastfeeding. LATCH was re-administered at the end of the 8th and 24th hour postpartum. Post-test data were obtained by administering LATCH and BSES at the end of the 48th hour postpartum.In statistical analysis; count, percentage distribution, arithmetic average, chi-square test, standard deviation, t-test in dependent and independent groups and ANOVA analysis in repeated measurements were used.

Enrollment

130 patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Being 18 years and older,
  • Having a full-term, single and healthy newborn,
  • Having no known health problems
  • Having no general anesthesia
  • Implementation of planned cesarean delivery,
  • Primiparous women who do not have a condition that prevents breastfeeding. Inclusion criteria of the research for infants

Exclusion criteria

• Women with a risky pregnancy diagnosis (such as preeclampsia, placenta previa, gestational diabetes)

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

130 participants in 2 patient groups

Experimental: experimental group
Experimental group
Description:
Biological Nutrition Technique
Treatment:
Other: Biological Nutrition Technique
Assigned Interventions
No Intervention group
Description:
standard care group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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