Effect of Hypnobreastfeeding Education in High-Risk Pregnant Women
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
AgeNot listed
SponsorAmasya University
About this trial
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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
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
Disqualifiers
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
Trial design
Design model
Parallel
Treatments tested in this trial
Hypnobreastfeeding Education
BehavioralMonitoring anxiety and breastfeeding intention in pregnancy, and assessing perception of insufficient milk supply, and breastfeeding adaptation in postpartum period
Treatment groups
68 Participants
are divided into 2 treatment groupsGroup A: Experimental groupExperimental treatment 1 intervention
Group B: Control groupNo intervention 0 interventions
Trial outcomes
Primary outcomes
1
Anxiety Assessment Scale
The minimum score that can be obtained from the scale is "10", the maximum score is "50", and as the score obtained from the scale increases, anxiety levels also increase.
Time frame
At the end of the 1 months2
Infant Feeding Intention Instrument
The minimum score that can be obtained from the scale is "0", the maximum score is "16", and as the score obtained from the scale increases, intention to exclusively breastfeed the baby levels also increase.
Time frame
At the end of the 1 monthsSecondary outcomes
1
Perception of Insufficient Milk Questionnaire
The minimum score that can be obtained from the scale is "0", the maximum score is "50", and as the score obtained from the scale increases, perception of milk sufficiency levels also increase.
Time frame
Postpartum 24-48 hours, postpartum 2nd week and postpartum 4th week2
Breastfeeding Adaptation Scale
The minimum score that can be obtained from the scale is "27", the maximum score is "135", and as the score obtained from the scale increases, breastfeeding adaptation levels also increase.
Time frame
Postpartum 24-48 hours, postpartum 2nd week and postpartum 4th weekSponsors and contacts
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Source ClinicalTrials.gov