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Virtual Reality and Simulation-Based Breastfeeding Training

The Effect of Virtual Reality and Simulation-Based Breastfeeding Education on Breastfeeding Efficacy, Success, and Maintenance of Breastfeeding in Mothers Experiencing Breastfeeding Problems in the Postpartum Period: A Randomized Controlled Experimental Study

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07768527
Enrollment
159
Registered
2026-08-17
Start date
2026-09-01
Completion date
2027-04-01
Last updated
2026-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lactation Power, Lactation Success, Maintenance of Breastfeeding, Postpartum Women

Brief summary

The aim of this study is to determine the effect of virtual reality and simulation-based breastfeeding education given to mothers experiencing breastfeeding problems in the postpartum period on breastfeeding potency, breastfeeding success, and breastfeeding continuation. The research is a randomized controlled experimental study.

Detailed description

The study population will consist of postpartum women who apply to the Lactation Counseling Clinic of the Obstetrics and Gynecology and Pediatric Hospital. The sample will consist of women who voluntarily participate in the study. Data will be collected through face-to-face interviews. Data will be collected by completing the "Personal Information Form", the "Mother's Breastfeeding Ability Scale" and the "Bristol Breastfeeding Assessment Scale".

Interventions

BEHAVIORALVirtual Reality Group

Mothers in this group will receive breastfeeding training using virtual reality glasses.

Mothers in this group will receive breastfeeding training using wearable nursing covers and newborn baby mannequins.

BEHAVIORALcontrol group

Mothers in this group will receive breastfeeding training as part of routine hospital protocol.

Sponsors

Cukurova University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 49 Years
Healthy volunteers
Yes

Inclusion criteria

* Primiparous * Infant in the neonatal period * Over 18 years of age * Term delivery * Healthy baby and individual * No communication barriers * Willing to participate in the study * Able to read and write Turkish

Exclusion criteria

* Multiparous * Infant not in the neonatal period * Under 18 years of age * Premature delivery * Unhealthy baby and individual * No communication barriers * Unwilling to participate in the study * Unable to read and write Turkish

Design outcomes

Primary

MeasureTime frameDescription
Mother's Breastfeeding Strength Scaleup to 12 monthsThis is a 37-item, 5-point Likert-type scale developed to assess mothers' breastfeeding strength level. Scale items are scored from "1 = Strongly disagree" to "5 = Strongly agree." There are no reverse-scored items. The total score ranges from 37 to 185. A higher total score indicates a higher level of breastfeeding strength in the mother. Subscale scores are calculated by summing the items in the relevant subscale. Higher scores indicate a more positive situation in terms of breastfeeding knowledge and skills, perceived competence, beliefs about breastfeeding, coping with breastfeeding problems, providing family support, and breastfeeding self-efficacy.

Secondary

MeasureTime frameDescription
Bristol Breastfeeding Assessment Scaleup to 12 monthsDeveloped by Jenny Ingram in 2014 and adapted into Turkish by Dolgun et al. in 2017, the scale is designed to assess common breastfeeding problems and adequacy in the postpartum period. The mother is observed by a midwife/nurse during breastfeeding, and the form is completed based on the criteria, evaluating both mother and baby. The application time is 5-10 minutes. While the original version of the scale had a Cronbach's Alpha of 0.68, the Turkish adaptation yielded 0.77. In our study, the reliability coefficient was determined to be 0.87. The measurement tool is a Likert-type scale consisting of 4 items: "positioning," "holding," "sucking," and "swallowing."

Contacts

CONTACTElif DAĞLI, Associate Professor
elifarik90@gmail.com+903223386560

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 18, 2026