The Effect of Hypno-Lactation Counseling on Breastfeeding Self-Efficacy and Breastfeeding Success in Adolescent Pregnant Women
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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 training and consultancy.
- Who it may be relevant to
- Registry conditions: Pregnant Women. Basic parameters: 16 years — 19 years · 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
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
The Effect of Hypnobreastfeeding Philosophy-Based Counseling on Breastfeeding Self-Efficacy and Breastfeeding Success in Adolescent Pregnant Women
Overview
This study aimed to investigate the effects of counseling based on hypno-breastfeeding philosophy on breastfeeding self-efficacy and breastfeeding success in pregnant adolescents. Research Hypotheses H1a: The intervention group\'s breastfeeding self-efficacy after hypno-breastfeeding counseling is different from the control group. H1b: The intervention group\'s breastfeeding success after hypno-breastfeeding counseling is different from the control group. This thesis is a randomized controlled experimental study. The study is planned to be conducted with two parallel groups, namely the intervention and control groups. Hypno-breastfeeding training will be applied to the intervention group, and standard breastfeeding training will be applied to the control group. The study will be conducted with pregnant adolescents who applied to the pregnancy clinic of Adıyaman University Training and Research Hospital between December 2024 and April 2025.
Detailed description
This study aimed to investigate the effects of counseling based on hypno-breastfeeding philosophy on breastfeeding self-efficacy and breastfeeding success in pregnant adolescents.
Place, type and time of the study This thesis study is a randomized controlled experimental study. The study is planned to be conducted with two parallel groups, the intervention and control groups. Hypno-breastfeeding training will be applied to the intervention group, and standard breastfeeding training will be applied to the control group. The study will be conducted with pregnant adolescents who applied to the pregnancy clinic of Adıyaman University Education and Research Hospital between December 2024 and April 2025.The Universe and Sample of the Study: The universe of the study consists of pregnant adolescents registered at the 400-bed Adıyaman University Training and Research Hospital.
Data Collection Tools Data will be collected using the Personal Information Form (Appendix 1), Breastfeeding Self-Efficacy Scale-Short Form (Appendix 2) and Breastfeeding Diagnostic Scale (LATCH) (Appendix 3) prepared by the researchers in line with the literature.
Interventions
- Behavioral Hypnobreastfeeding training and consultancy
Hypno-breastfeeding Education Group A counseling program based on hypno-breastfeeding philosophy, where 4-week education content will be presented to pregnant adolescents in their 28-30th week of pregnancy and applications will be made, will be implemented with 4 sessions and 6 follow-up
Primary outcome measures
- Breastfeeding Self-Efficacy [Time frame: Baseline, 4 week, and after the labour]
Secondary outcome measures (1)
- Breastfeeding Success [Time frame: Baseline, 4 week, and after the labour]
Eligibility criteria
Inclusion criteria
- Between the ages of 16-19,
- Single pregnancy,
- Primiparous,
- Planning a normal vaginal birth,
- In the last trimester of pregnancy,
- No communication problems,
- Can speak and understand Turkish,
- Can read and write, as the scales must be filled out by the individual,
- No condition preventing breastfeeding,
- Not receiving any training/counseling regarding breastfeeding during pregnancy
Exclusion criteria
- Women who have been diagnosed with a psychiatric disorder,
- Complications in the mother and baby (chronic disease in the mother that prevents breastfeeding; diabetes, hypertension, etc. fetal anomalies in the fetus, postpartum discomfort that will prevent breastfeeding),
- Women who develop a health problem during pregnancy during the training process,
- Women who want to withdraw from the study voluntarily
- Women who have any disability (hearing impairment, etc.) will be excluded from the study.
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
- Sequential
- Masking
- Single blind
- Primary purpose
- Supportive care
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06746662 · ipekt1