ClinicalTrials.gg
Not yet recruitingNCT07346482Infant CareUpdated Jan 20, 2026

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

An interventional study of Education in Infant Death, Infant Care and Midwifery, sponsored by Cukurova University. Not yet recruiting at 1 site in Turkey (Türkiye). Open to female participants, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-20.

Sponsored by Cukurova University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Sex
Female
01

Study 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.

Read the 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.

02

Conditions studied

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

Browse trials for

Keywords

  • infant
  • infant death
  • midwifery care
  • accident
  • education
03

In context

Infant Death

51 studies on the registry are indexed under Infant Death; 15 are open to participants now.

This study's planned enrollment of 120 is below the median of 4,287 across 40 interventional studies indexed under Infant Death.

Browse Infant Death studies →

Lead sponsor

Cukurova University is the lead sponsor of 259 studies on the registry; 50 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • Diagnosed high-risk pregnancy
  • Diagnosed mental health condition
  • Having previously received training/course in safe infant care
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
120 participants (estimated)

Study arms

  • 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.

    Other: Education

  • No intervention
    Control

    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.

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.

06

What researchers measure

Primary outcomes

  1. Home Accident Awareness Scale for Mothers

    Items are scored on a scale of 1-5. As the scale score increases, mothers' awareness of household accidents will increase.

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

  2. Sudden Infant Death Syndrome Awareness Scale - Mother Form

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

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

07

Study locations

1 site
  • Cukurova University Faculty of Health Sciences Department of Midwifery
    Adana, Saricam 01330, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Feb 2026; primary completion for Dec 2026, 10 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 8, 2026
First posted
Jan 16, 2026
StartEst.
Feb 16, 2026
Primary completionEst.
Dec 31, 2026
CompletionEst.
Jan 20, 2027
Last update
Jan 20, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jan 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07346482
Responsible party
Ayseren Cevik (Principal Investigator,, Cukurova University) — Principal investigator
First posted
Jan 16, 2026
Start date
Feb 16, 2026 (estimated)
Primary completion
Dec 31, 2026 (estimated)
Completion
Jan 20, 2027 (estimated)
Last update
Jan 20, 2026

Study contacts

Ayseren Cevik, PhD
Contact
acevik@cu.edu.tr
+90 (322) 338 64 84 ext. 1129
Cagla Kilic, Msc student
Contact
cagla.kilic15@outlook.com
+90 (322) 338 64 84 ext. 1124

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion