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The Effects of Hypnobreastfeeding and Oxytocin Massage on Breastfeeding (HBOM)

2 november 2026 bijgewerkt door: Sümeyye ALTIPARMAK

The Effect of Hypno-breastfeeding and Oxytocin Massage on Breastfeeding Motivation, Perceived Insufficient Milk Supply, Mother-to-Infant Bonding and Uterus Involution in Primiparas: A Randomized Controlled Trial

This study examined whether hypno-breastfeeding and oxytocin massage could improve breastfeeding motivation, mothers' perceptions of their milk supply, mother-to-infant bonding, and uterine recovery after childbirth in first-time mothers.

The study included 270 women at a public hospital in eastern Türkiye between September 2020 and March 2021. Participants were divided into three groups of 90 women each.

Women in the hypno-breastfeeding group received guidance on relaxation, positive affirmations, imagination, and visualization during late pregnancy and after childbirth. Women in the oxytocin massage group received two back massage sessions after childbirth. Women in the control group received routine care without either of these additional interventions.

On the first day after childbirth, the researchers assessed breastfeeding motivation, perceived milk supply, mother-to-infant bonding, and uterine recovery to compare the three groups.

Studie Overzicht

Toestand

Voltooid

Conditie

Interventie / Behandeling

Gedetailleerde beschrijving

This study was conducted using a three-arm experimental design with a post-test control group at a public hospital in eastern Türkiye between September 2020 and March 2021. Data were collected by the researcher through face-to-face interviews with pregnant women attending the non-stress test (NST) unit and postpartum women admitted to the puerperal ward.

The study included 270 primiparous women, with 90 participants in each of three groups: hypno-breastfeeding, oxytocin massage, and routine care.

Pregnant women were recruited into the hypno-breastfeeding group according to their order of arrival at the NST unit. Postpartum women were assigned to the oxytocin massage or control group using a computer-based randomization procedure. A total of 180 numbered positions were generated for these two groups, with 90 women allocated to each group. Participants in the oxytocin massage and control groups were recruited from separate rooms to reduce the risk of infection.

The hypno-breastfeeding intervention began at 37-38 weeks of gestation and was repeated at 39-40 weeks. Participants received education and guidance on positive affirmations, relaxation, imagination, and visualization techniques, supported by educational materials, home exercises, telephone calls, and text messages. Two additional hypno-breastfeeding sessions were provided on the first postpartum day, before the first breastfeeding session and between 16 and 20 hours after childbirth.

Participants in the oxytocin massage group received two massage sessions on the first postpartum day, before the first breastfeeding session and between 16 and 20 hours after childbirth. The massage was performed in a quiet and private environment, focusing on the back and spinal region around the fifth and sixth ribs.

Participants in the control group received routine postpartum care without the study-specific hypno-breastfeeding or oxytocin massage interventions.

Outcome assessments were performed on the first postpartum day before hospital discharge. Breastfeeding motivation, perceived milk supply, and mother-to-infant bonding were evaluated using standardized questionnaires. Uterine recovery was assessed by measuring the distance between the uterine fundus and the symphysis pubis with a measuring tape after bladder emptying.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

270

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

  • Turkije (Türkiye)
    • Malatya
      • Malatya, Malatya, Turkije (Türkiye), 44280
        • Malatya Training and Research Hospital - Women's, Maternity and Children's Hospital

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Kind
  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Ja

Geslachten die in aanmerking komen voor studie

Vrouw

Beschrijving

Study Inclusion Criteria:

For pregnants;

  • Having a healthy singleton pregnancy of 37 weeks and above,
  • Having no communication barrier,
  • Having no diagnosed psychiatric issues. For puerperants;
  • Having a normal delivery,
  • Having no complications for herself and her baby in the postpartum period,
  • Having consumed no herbal or other food/beverage to support breastfeeding in the postpartum period,
  • Having no barriers to breastfeeding in the postpartum period (having a newborn in intensive care, having skin issues such as nipple cracks and inverted nipples, etc.),
  • Having no communication barrier,
  • Having no diagnosed psychiatric issues. Study Exclusion Criteria; For pregnants;
  • Having developed cesarean section indication in delivery. For puerperants;
  • Having any condition causing her to be separated from her baby in the postpartum period.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Ondersteunende zorg
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Hypno-breastfeeding Group

Participants received hypno-breastfeeding education and practice sessions during late pregnancy and on the first postpartum day. The intervention included relaxation, positive affirmations, imagination, and visualization techniques.
Gedragsmatig: Hypno-breastfeeding

The hypno-breastfeeding intervention was initiated at 37-38 weeks of gestation and repeated at 39-40 weeks during visits to the non-stress test (NST) unit. Participants received education and guidance on relaxation, positive affirmations, imagination, and visualization techniques to support breastfeeding. Educational brochures and home exercises were provided, and participants were supported through telephone calls and text messages. On the first postpartum day, two additional hypno-breastfeeding sessions were conducted: one before the first breastfeeding session and another between 16 and 20 hours after childbirth.
Experimenteel: Oxytocin Massage Group

Participants received two oxytocin massage sessions on the first postpartum day, before the first breastfeeding session and between 16 and 20 hours after childbirth.
Ander: Oxytocin Massage

Participants received two oxytocin massage sessions on the first postpartum day. The first session was administered before the first breastfeeding session, and the second session was conducted between 16 and 20 hours after childbirth. The massage was performed in a quiet and private environment. Participants were seated in a forward-leaning position with their head resting on their arms or a table. Massage was applied to the back along the spinal region, particularly around the level of the fifth and sixth ribs, to support breastfeeding and postpartum recovery.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Breastfeeding Motivation Assessed Using the Primiparous Breastfeeding Motivation Scale (PBMS)
Tijdsspanne: Postpartum day 1, before hospital discharge.

Breastfeeding motivation was assessed using the Primiparous Breastfeeding Motivation Scale (PBMS). Items are rated on a 7-point Likert scale. Subscale scores are calculated and interpreted separately, with higher scores indicating higher levels of the corresponding breastfeeding motivation dimension. No overall cut-off score is used.
Postpartum day 1, before hospital discharge.
Perceived Milk Supply Adequacy Assessed Using the Perceived Insufficient Milk Supply Questionnaire (PIMSQ)
Tijdsspanne: Postpartum day 1, before hospital discharge.

Perceived milk supply adequacy was evaluated using the Perceived Insufficient Milk Supply Questionnaire (PIMSQ). Total scores range from 0 to 50, with higher scores indicating greater perceived milk supply adequacy and lower perceived insufficient milk supply.
Postpartum day 1, before hospital discharge.
Mother-to-Infant Bonding Assessed Using the Mother-to-Infant Bonding Scale (MIBS)
Tijdsspanne: Postpartum day 1, before hospital discharge.

Mother-to-infant bonding was assessed using the Mother-to-Infant Bonding Scale (MIBS). Total scores range from 0 to 24, with higher scores indicating greater difficulties in mother-to-infant bonding.
Postpartum day 1, before hospital discharge.
Postpartum Uterine Fundal Height Measured Using the Uterine Involution Assessment Form (UIAF)
Tijdsspanne: Postpartum day 1, before hospital discharge.

Postpartum uterine involution was assessed using a researcher-developed Uterine Involution Assessment Form (UIAF). After the participant emptied her bladder, the distance between the uterine fundus and the symphysis pubis was measured in centimeters using a measuring tape. The same measuring tape was used for all assessments. The recorded measurement represented uterine fundal height on the first postpartum day.
Postpartum day 1, before hospital discharge.

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Sümeyye ALTIPARMAK

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Algemene publicaties

  • References 1. J. Stockdale, M. Sinclair, G. Kernohan, et al. Understanding motivational theory and the psychology of breastfeeding. In: Bryar R, Sinclair M (eds), Theory for midwifery practice: Palgrave Macmillan, 2011. 2. J. Stockdale, M. Sinclair, G. Kernohan, et al. Sensitivity of the breastfeeding motivational measurement scale: a known group analysis of first time mothers, PloS one 2013;8(12), e82976. 3. E. Koc, S. Ruzgar, S. Ozturk Altinayak, Determination of Factors affecting lactating women's perceptions of ınsufficient milk and the foods they use to ıncrease breast milk, Bezmialem Science 2024;12(3):280-7. https://doi.org/10.14235/bas.galenos.2024.56933 4. S.G. Caliskan, S. Altinkaynak, I'm Breastfeeding My Baby Doesn't Get Enough: Perception of Insufficient Milk, Sakarya University Journal of Holistic Health 2019;2(2), 1-9. 5. S. Ucan, The Effect of Breastfeeding Education Given to Parents on Breastfeeding Process, Cultural Behaviors and Parent-Infant Attachment. Institute of Health Sciences, Department of Public Health. PhD Thesis, Konya: Selcuk University, 2016. 6. E. Bianciardi, F. Ongaretto, A. De Stefano, et al., The mother-baby bond: Role of past and current relationships, Children 2023;10(3), 421. https://doi.org/10.3390/children10030421 7. G. Bosmans, L. Van Vlierberghe, M.J. Bakermans-Kranenburg, et al., A learning theory approach to attachment theory: Exploring clinical applications, Clinical child and family psychology review 2022;25(3), 591-612. https://doi.org/10.1007/s10567-021-00377-x 8. S. Topal, N. Çınar, S. Altınkaynak, Maternal Health Benefits of Breastfeeding, Journal of Human Rhythm 2017;3(1), 25-31. 9. K.A. Uctu, N. Ozerdoğan, Effect of teach-back method on breastfeeding success: A single blind randomized controlled study, Health Care for Women International 2023;44:3, 314-327, https://doi.org/10.1080/07399332.2021.201915 10. N. Irmak, Importance of breast milk and factors affecting exclusive breastfeeding for the first 6 months,

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

1 september 2020

Primaire voltooiing (Werkelijk)

31 maart 2021

Studie voltooiing (Werkelijk)

31 maart 2021

Studieregistratiedata

Eerst ingediend

2 november 2026

Eerst ingediend dat voldeed aan de QC-criteria

2 november 2026

Eerst geplaatst (Werkelijk)

6 november 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

6 november 2026

Laatste update ingediend die voldeed aan QC-criteria

2 november 2026

Laatst geverifieerd

1 maart 2021

Meer informatie

Termen gerelateerd aan deze studie

Trefwoorden

Aanvullende relevante MeSH-voorwaarden

Andere studie-ID-nummers

  • HBOM-2020-001

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

Individual participant data (IPD) will not be shared with other researchers due to participant confidentiality and privacy considerations. The study data will be retained and managed in accordance with the approved research protocol and applicable ethical requirements.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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