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Effect of Teach-Back Education on Breastfeeding and Bonding in Mothers of Preterm Infants (TEACH-PRE)

A

Ataturk University

Status

Enrolling

Conditions

Breast Feeding
Premature
Mother-Child Relationship

Treatments

Behavioral: Teach-Back Education

Study type

Interventional

Funder types

Other

Identifiers

NCT07371845
ATATURKU-HF-DAÖ-02

Details and patient eligibility

About

The aim of this randomized controlled experimental study is to contribute to the standardization of nursing interventions for premature mothers and to establish a scientific basis for breastfeeding education models in our country. It also aims to evaluate the effects of the following: digital privacy literacy, children's autonomy, decision-making ability, and privacy awareness. The hypotheses of the study are as follows:

H₁: Mothers who received Teach-Back training have a higher level of breastfeeding self-efficacy.

H₂: Mothers who received Teach-Back training have a higher level of mother-infant bonding.

H₀: There is no significant difference between the groups.

Full description

The study will be conducted with mothers of premature babies who meet the inclusion criteria at the state hospital located in Tatvan district, affiliated with the Bitlis Provincial Health Directorate. Participants will be assigned to two groups using simple random sampling:

  1. Experimental group: (Mothers who received Teach-Back training)
  2. Control group: (Mothers who received routine discharge education). Data will be collected using the "Participant Identification Form", "Breastfeeding Self-Efficacy Scale for Mothers of Preterm Babies", "Mother-Infant Bonding Scale" and "Teach-Back Training Evaluation Form".

Enrollment

102 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Being 18 years of age or older,
  • Having a baby born before the 37th week of gestation (being a mother of a premature baby),
  • Being able to read and understand Turkish,
  • Having actually started breastfeeding,
  • Having no hearing, visual, or cognitive communication impairment,
  • Not having a diagnosed serious psychiatric illness (major depression, anxiety disorder, etc.),
  • The baby not being in a serious clinical condition, not under palliative care or intensive life support,
  • Not participating in another breastfeeding education or counseling program at the same time,
  • Voluntarily agreeing to participate in the study.

Exclusion criteria

  • All mothers who do not meet the inclusion criteria will be excluded from the study.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

102 participants in 2 patient groups

Teach-back Education Group
Experimental group
Description:
Mothers receive teach-back education on breastfeeding and infant care.
Treatment:
Behavioral: Teach-Back Education
Control Group
No Intervention group
Description:
Mothers receive routine care without teach-back education.

Trial contacts and locations

1

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Central trial contact

devran atalay özkılıç, phD

Data sourced from clinicaltrials.gov

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