- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06493630
The Effect of Hypnobreastfeeding Education Given to Primiparas
December 13, 2025 updated by: Amasya University
The Effect of Hypnobreastfeeding Education Given to Primiparas on Breastfeeding Myths, Expectations and Self-Efficacy
Hypnobreastfeeding is one of the education-based interventions used in this field.
This study aims to evaluate the effect of hypnobreastfeeding education given to primiparous pregnant women on breastfeeding myths, breastfeeding expectations and breastfeeding self-efficacy.
According to the results of the power analysis, at least 104 pregnant women, 52 experimental and 52 control, should be included in the study.
Data were collected with the "Pregnant Introduction Form", "Breastfeeding Myths Scale", "Breastfeeding Expectations Scale-A" and "Prenatal Breastfeeding Self-Efficacy Scale".
In the research, hypnobreastfeeding training was applied by the researcher to the primiparous pregnant women in the experimental group.
The study was completed with 110 primiparous pregnant women, 54 in the experimental group and 56 in the control group.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Primiparous pregnant women may need support regarding the breastfeeding process because they have not had breastfeeding experience before.
Negative breastfeeding stories and misinformation can affect beliefs, attitudes, and fears about breastfeeding.
Education-based interventions provided by health professionals can be beneficial in reducing false beliefs and myths about breastfeeding, reducing breastfeeding-related fears/anxious expectations, and increasing breastfeeding self-efficacy.
Hypnobreastfeeding is one of the education-based interventions used in this field.
This study aims to evaluate the effect of hypnobreastfeeding education given to primiparous pregnant women on breastfeeding myths, breastfeeding expectations and breastfeeding self-efficacy.
According to the results of the power analysis, at least 104 pregnant women, 52 experimental and 52 control, should be included in the study.
Data were collected with the "Pregnant Introduction Form", "Breastfeeding Myths Scale", "Breastfeeding Expectations Scale-A" and "Prenatal Breastfeeding Self-Efficacy Scale".
In the research, hypnobreastfeeding training was applied by the researcher to the primiparous pregnant women in the experimental group.
The study was completed with 110 primiparous pregnant women, 54 in the experimental group and 56 in the control group.
Study Type
Interventional
Enrollment (Actual)
110
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Amasya, Turkey (Türkiye), 05100
- Emine İBİCİ AKÇA
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Primiparous pregnant women,
- Singleton pregnancy,
- Those with 28-32 weeks of pregnancy,
- Those who can read and write Turkish,
- Those who volunteered to participate in the study
Exclusion Criteria:
- Those with communication disabilities,
- Those with psychiatric and mental illnesses,
- Those who have an obstacle to breastfeeding,
- Those diagnosed with risky pregnancy,
- Those who have previously attended a birth preparation class,
- Those who receive breastfeeding-related training and consultancy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control group
Control
|
|
|
Experimental: Experimental group
Hypnobreastfeeding Education
|
Hypnobreastfeeding Education: Monitoring breastfeeding myths, breastfeeding expectations and breastfeeding self-efficacy with hypnobreastfeeding education
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Breastfeeding Myths Scale
Time Frame: At the end of the 1 months
|
The minimum score that can be obtained from the scale is "30", the maximum score is "150", and as the score obtained from the scale decreases, breastfeeding myths levels also decrease.
|
At the end of the 1 months
|
|
Breastfeeding Expectations Scale-A
Time Frame: At the end of the 1 months
|
The minimum score that can be obtained from the scale is "12", the maximum score is "60".
Lower scores from the scale indicate more positive expectations regarding the breastfeeding experience.
|
At the end of the 1 months
|
|
Prenatal Breastfeeding Self-Efficacy Scale
Time Frame: At the end of the 1 months
|
The minimum score that can be obtained from the scale is "20", the maximum score is "100", and as the score obtained from the scale increases, breastfeeding self-efficacy levels also increase.
|
At the end of the 1 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Emine İbici Akça, Amasya University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 1, 2024
Primary Completion (Actual)
February 1, 2025
Study Completion (Actual)
May 31, 2025
Study Registration Dates
First Submitted
July 2, 2024
First Submitted That Met QC Criteria
July 2, 2024
First Posted (Actual)
July 10, 2024
Study Record Updates
Last Update Posted (Actual)
December 19, 2025
Last Update Submitted That Met QC Criteria
December 13, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Amasya Uni_emine.akca
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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