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

Çukurova University

Status: Begins enrollment this month

Conditions: Infant Death; Education; Infant Care; Midwifery; Accident at Home

Treatments: Other: Education

Study type: Interventional

Funder types: Other

Identifiers

NCT07346482

96/160 (14.11.2025)

Details and patient eligibility

About

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.

Full 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.

Enrollment: 120 estimated patients

Sex: Female

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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120 participants in 2 patient groups

Experimental

Experimental group

Description:

Following the pre-test, the intervention group will receive training on safe infant care. A final test will be administered via telephone in the second week postpartum.

Treatment:

Other: Education

Control

No Intervention group

Description:

Standard care (Turkish Ministry of Health Prenatal Care Guide) will be applied during the follow-up care after the pre-test. A final test will be administered via telephone in the second week postpartum.