The Effect of Breastfeeding Training Given to Mothers With Vaginal Birth by Motivational Interview Technique

NCT ID: NCT06313034

Last Updated: 2024-03-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-05-01

Study Completion Date

2024-03-15

Brief Summary

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This study aimed to determine the effect of breastfeeding education given to mothers who gave birth vaginally using motivational interviewing technique on breastfeeding motivation, self-efficacy and attachment. The study will be conducted as a single-blind, randomized controlled trial.

Detailed Description

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The study will be conducted as a single-blind, randomized controlled trial with 80 mothers who gave birth vaginally. In the experimental group, just before discharge from the hospital (within the last 4 hours before discharge), on the 2nd-5th, 13th-17th, 30th-42nd days after birth. Breastfeeding training based on motivational interviewing technique will be given 4 times in total. The control group will continue to receive the current standard care and service of the relevant hospital and other postpartum health institutions.

Hypotheses of the Research

1. The effect of breastfeeding education given to mothers who gave birth vaginally with motivational interviewing technique on increasing the mother's breastfeeding motivation.

are there?(H1)
2. Breastfeeding education given to mothers who gave birth vaginally with motivational interviewing technique has no effect on increasing the mother's breastfeeding self-efficacy.

Does it have any effect?(H2)
3. The effect of breastfeeding education given to mothers who gave birth vaginally with motivational interviewing technique on increasing the level of mother-infant attachment.

are there?(H3)

Conditions

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Breastfeeding

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The sample of the research will consist of mothers who gave primary vaginal birth (40 experimental group and 40 control group)
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants
While it is known by the researcher whether the mothers are in the experimental or control group, it is not known by the mother.

Study Groups

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experimental group

Breastfeeding education will be given to mothers in the experimental group in 4 individual and face-to-face sessions based on motivational interviewing technique.

The first session of breastfeeding training based on motivational interviewing technique will be held in the delivery room where the mother is hospitalized before being discharged from the hospital. Other sessions will be held according to the monitoring frequency recommended in the Postnatal Care Management Guide of the Ministry of Health of the Republic of Turkey (2018). These will be done at the health institution where the mother receives service.

Second session; Between the 2th and 5th postpartum day Third session; Between the 13th and 17th postpartum day Fourth session; Between the 30th and 42th postpartum day The duration of each motivational interview is planned to be between 30-40 minutes on average.

Group Type EXPERIMENTAL

Breastfeeding education based on motivational interviewing technique

Intervention Type BEHAVIORAL

Breastfeeding education based on motivational interviewing technique; Breast milk properties, benefits to mother and baby, breastfeeding positions, the relationship between breastfeeding and attachment, signs of hunger in the newborn, Breastfeeding frequency, duration and termination, Breast milk expressing methods, Expressions showing that the newborn has enough milk, Breast milk storage will cover the topics. These topics will be given based on motivational interviewing technique.

According to the motivational interviewing technique, the mother's "intention, importance and confidence-sufficiency" regarding breastfeeding will be determined and firstly, an agenda will be created on "issues related to breastfeeding with the mother". Each session will be conducted by following the "open-ended questioning, verification, reflective listening and summarizing" approaches of the motivational interviewing technique.

control group

Before discharge, mothers in the control group will be given routine breastfeeding training by the midwife working in the delivery room in accordance with the mother/baby friendly hospital protocol.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Breastfeeding education based on motivational interviewing technique

Breastfeeding education based on motivational interviewing technique; Breast milk properties, benefits to mother and baby, breastfeeding positions, the relationship between breastfeeding and attachment, signs of hunger in the newborn, Breastfeeding frequency, duration and termination, Breast milk expressing methods, Expressions showing that the newborn has enough milk, Breast milk storage will cover the topics. These topics will be given based on motivational interviewing technique.

According to the motivational interviewing technique, the mother's "intention, importance and confidence-sufficiency" regarding breastfeeding will be determined and firstly, an agenda will be created on "issues related to breastfeeding with the mother". Each session will be conducted by following the "open-ended questioning, verification, reflective listening and summarizing" approaches of the motivational interviewing technique.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

Maternal criteria;

* Agreeing to participate in the research
* Being 20 years or older
* Having had a vaginal birth
* being primiparous
* Being at least a primary school graduate
* Ability to speak Turkish
* Not having any condition that would prevent communication
* No medical breast problem

Criteria for the baby;

* Being born at term (38-41 gestational weeks)
* There is no congenital anomaly such as cleft palate or lip of the newborn that may prevent sucking.
* Birth weight over 2500 grams

Exclusion Criteria

Maternal criteria;

* Having a chronic disease that prevents breastfeeding
* Having major breast problems that will prevent breastfeeding
* The mother has a diagnosed psychiatric disease
* Having 2 or more live newborns in this birth

Criteria for the baby;

* Premature birth (37th gestational week and before)
* Having a congenital disease
* Being in the risk group/being diagnosed with a disease in the newborn screening program
Minimum Eligible Age

20 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Karadeniz Technical University

OTHER

Sponsor Role collaborator

Gümüşhane Universıty

OTHER

Sponsor Role lead

Responsible Party

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Özge PALANCI AY

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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ÖZGE PALANCI AY

Role: PRINCIPAL_INVESTIGATOR

Gümüşhane Universıty

SONGÜL AKTAŞ

Role: PRINCIPAL_INVESTIGATOR

Karadeniz Technical University

Locations

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Gümüşhane University

Gümüşhane, , Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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ÖZGE PALANCI AY

Role: CONTACT

05428933629

SONGÜL AKTAŞ

Role: CONTACT

05326475261

Facility Contacts

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ÖZGE PALANCI AY

Role: primary

Other Identifiers

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GU-SBF-OPA-02

Identifier Type: -

Identifier Source: org_study_id

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