Effect of Hypnobreastfeeding Education in High-Risk Pregnant Women
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Hypnobreastfeeding Education.
- Who it may be relevant to
- Registry conditions: High-risk Pregnancy, Breast Feeding. Basic parameters: No limits · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Turkey (Türkiye)
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
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
Overview
It is thought that hypnobreastfeeding training given to high-risk pregnant women will reduce anxiety levels, increase lactation, encourage breastfeeding, reduce the perception of insufficient milk, and facilitate adaptation to the postpartum breastfeeding process. According to the results of the power analysis, at least 68 high-risk pregnant women, 34 experimental and 34 control, should be included in the study. Data will be collected with the "Pregnancy Information Form", "Anxiety Assessment Scale", " Infant Feeding Intention Instrument", "Postpartum Information Form", "Perception of Insufficient Milk Questionnaire" and "Breastfeeding Adaptation Scale". In the research, hypnobreastfeeding training will be applied by the researcher to the high-risk pregnant women in the experimental group.
Detailed description
Hypnobreastfeeding training provided to high-risk pregnant women is believed to reduce anxiety, increase lactation, encourage breastfeeding, reduce the perception of insufficient milk supply, and facilitate postpartum breastfeeding adaptation. This will ensure the baby receives adequate and healthy nutrition and the mother's self-confidence increases. Furthermore, hypnobreastfeeding training will contribute to a more comfortable, informed, and peaceful breastfeeding experience for the mother. This will positively impact both the pregnancy and the health of both mother and baby. The study was planned to evaluate the effects of hypnobreastfeeding training given to high-risk pregnant women on anxiety levels, breastfeeding intentions, postpartum perception of insufficient milk, and breastfeeding adaptation. According to the results of the power analysis, at least 68 high-risk pregnant women, 34 experimental and 34 control, should be included in the study. Data will be collected with the "Pregnancy Information Form", "Anxiety Assessment Scale", " Infant Feeding Intention Instrument", "Postpartum Information Form", "Perception of Insufficient Milk Questionnaire" and "Breastfeeding Adaptation Scale". In the research, hypnobreastfeeding training will be applied by the researcher to the high-risk pregnant women in the experimental group.
Interventions
- Behavioral Hypnobreastfeeding Education
Monitoring anxiety and breastfeeding intention in pregnancy, and assessing perception of insufficient milk supply, and breastfeeding adaptation in postpartum period
Primary outcome measures
- Anxiety Assessment Scale [Time frame: At the end of the 1 months]
- Infant Feeding Intention Instrument [Time frame: At the end of the 1 months]
Secondary outcome measures (2)
- Perception of Insufficient Milk Questionnaire [Time frame: Postpartum 24-48 hours, postpartum 2nd week and postpartum 4th week]
- Breastfeeding Adaptation Scale [Time frame: Postpartum 24-48 hours, postpartum 2nd week and postpartum 4th week]
Eligibility criteria
Inclusion criteria
- High-risk primiparous pregnant women
- Those with 28-34 weeks of pregnancy
- Those who volunteered to participate in the study
- Those who can read and write Turkish
Exclusion criteria
- Those with communication disabilities
- Those with psychiatric and mental illnesses
- Those who have an obstacle to breastfeeding
- Those who have previously attended a birth preparation class
- Those who receive breastfeeding-related training and consultancy
- Those who gave birth prematurely
- Those with anomalies in their babies
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
Turkey (Türkiye) · 1 center
- Amasya University — Amasya
Identifiers
NCT: NCT07281339 · 2025000162