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Determining the Effect of Midwife-Led Safe Infant Care Training for Pregnant Women on Awareness of Sudden Infant Death Syndrome and Home Accidents

Determining the Effect of Midwife-Led Safe Infant Care Training for Pregnant Women on Awareness of Sudden Infant Death Syndrome and Home Accidents

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07346482
Acronym
Infant Care
Enrollment
120
Registered
2026-01-16
Start date
2026-02-16
Completion date
2027-01-20
Last updated
2026-01-20

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

Conditions

Accident at Home, Education, Infant Care, Infant Death, Midwifery

Keywords

infant, infant death, midwifery care, accident, education

Brief summary

This project is a pioneering study in determining the impact of midwife-led safe infant care training for pregnant women on awareness of sudden infant death syndrome (SIDS) and home accidents. Raising awareness and improving women's knowledge about SIDS and home accidents is expected to help reduce preventable infant deaths. If the effectiveness of this training is proven, integrating it into prenatal care programs would be a significant step towards improving maternal and child health.

Detailed description

This research is designed as a randomized controlled experimental study. The research will be conducted in the NST unit located in the Marsa Obstetrics and Gynecology Annex Building of Seyhan State Hospital between the specified dates. It has been determined that 60 participants should be included in the intervention group and 60 in the control group. Primiparous pregnant women ≥32 weeks of gestation will be included in the study. The study will be conducted in two interviews. The pre-test will be administered at the first meeting with the pregnant woman, and the post-test will be administered in the second week postpartum. The independent variables of the study are safe infant care education, and the demographic and obstetric characteristics of the pregnant women. The dependent variables are awareness of sudden infant death syndrome and scores on the home accident awareness scale for mothers. After normality tests are performed, univariate and multivariate analyses appropriate to the data set will be performed, and a significance level of p\<0.05 will be considered. The Statistical Programme for Social Science 22 (SPSS) will be used for data analysis.

Interventions

OTHEREducation

The educational content consists of general information about sudden infant death syndrome and home accidents in children aged 0-3, as well as prevention methods.

Sponsors

Cukurova University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* Volunteering to participate in the research * Being able to speak and understand Turkish * Being literate * Being a primiparous pregnant woman (due to the greater need for information) ≥36th week of pregnancy (because it is close to delivery and there is sufficient time to translate what they have learned into behavior)

Exclusion criteria

* Diagnosed high-risk pregnancy * Diagnosed mental health condition * Having previously received training/course in safe infant care

Design outcomes

Primary

MeasureTime frameDescription
Home Accident Awareness Scale for Motherspre-intervention, immediately after the intervention, after 2 weekItems are scored on a scale of 1-5. As the scale score increases, mothers' awareness of household accidents will increase.
Sudden Infant Death Syndrome Awareness Scale - Mother Formpre-intervention, immediately after the intervention, after 2 weekItems are scored on a scale of 1 to 5. As the score obtained from the scale increases, the awareness score decreases.

Countries

Turkey (Türkiye)

Contacts

CONTACTAyseren Cevik, PhD
acevik@cu.edu.tr+90 (322) 338 64 84
CONTACTCagla Kilic, Msc student
cagla.kilic15@outlook.com+90 (322) 338 64 84

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026