Actively Recruiting

Phase Not Applicable
FEMALE
Healthy Volunteers
ID07281339

The Effect of Hypnobreastfeeding Education Given to High-Risk Pregnant Women on Anxiety Levels, Infant Feeding Intention, Postpartum Perception of Insufficient Milk, and Breastfeeding Adaptation

Led by Amasya University · Updated on 2025-12-15

68

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of hypnobreastfeeding training on high-risk pregnant women, focusing on reducing anxiety, increasing milk production, encouraging breastfeeding, and improving adaptation to breastfeeding after birth. The study aims to support both mother and baby's health by enhancing the breastfeeding experience and boosting the mother's confidence. This research will measure anxiety levels, breastfeeding intentions, perceptions of milk supply, and adaptation to breastfeeding among first-time mothers at risk during pregnancy. Participants will be randomly assigned to one of two groups: an experimental group receiving hypnobreastfeeding education and a control group with no intervention. The hypnobreastfeeding training will be provided by the researcher to the experimental group during pregnancy, while the control group will receive standard care. The study involves collecting data through several forms and questionnaires related to pregnancy, anxiety, infant feeding intentions, postpartum experiences, perception of milk sufficiency, and breastfeeding adaptation. Participants will be assessed using various tools including the Anxiety Assessment Scale and Infant Feeding Intention Instrument at one month postpartum. Additional evaluations using the Perception of Insufficient Milk Questionnaire and Breastfeeding Adaptation Scale will occur at 24-48 hours, two weeks, and four weeks after birth. The study will monitor outcomes and gather comprehensive data on the breastfeeding process, maternal anxiety, and infant feeding, concluding with analysis after these time points. The total participation duration spans from late pregnancy through the first month postpartum.

CONDITIONS

Brief Title

Effect of Hypnobreastfeeding Education in High-Risk Pregnant Women

Who Can Participate

FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • High-risk primiparous pregnant women
  • Between 28 and 34 weeks of pregnancy
  • Volunteered to participate in the study
  • Able to read and write Turkish
Not Eligible

You will not qualify if you...

  • Communication disabilities
  • Psychiatric and mental illnesses
  • Obstacles to breastfeeding
  • Previously attended a birth preparation class
  • Received breastfeeding-related training or consultancy
  • Premature birth
  • Babies with anomalies

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

Duration - Up to 1 month

Participants receive hypnobreastfeeding education aimed at reducing anxiety and improving breastfeeding outcomes.

1 baseline visit and weekly visits during the 1-month education period

Follow-up

Duration - 4 weeks postpartum

Participants are monitored postpartum for perception of milk supply and breastfeeding adaptation.

3 visits at 24-48 hours, 2 weeks, and 4 weeks postpartum

Trial Site Locations

Total: 1 location

1

Amasya University

Amasya, Turkey (Türkiye), 05000

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Research Team

E

Emine İbici Akça

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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