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Clinical Trials/NCT07346482
NCT07346482
Not yet recruiting
Not Applicable

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

Cukurova University1 site in 1 country120 target enrollmentStarted: February 16, 2026Last updated:
InterventionsEducation

Overview

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
120
Locations
1
Primary Endpoint
Home Accident Awareness Scale for Mothers

Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Participant)

Eligibility Criteria

Sex
Female
Accepts 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

Arms & Interventions

Experimental

Experimental

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.

Intervention: Education (Other)

Control

No Intervention

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.

Outcomes

Primary Outcomes

Home Accident Awareness Scale for Mothers

Time Frame: pre-intervention, immediately after the intervention, after 2 week

Items 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 Form

Time Frame: pre-intervention, immediately after the intervention, after 2 week

Items are scored on a scale of 1 to 5. As the score obtained from the scale increases, the awareness score decreases.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ayseren Cevik

Principal Investigator,

Cukurova University

Study Sites (1)

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