This randomized controlled trial aims to evaluate the effect of using the ABÖS-M mobile application, developed for mothers with newborns, on maternal knowledge, care skills, and self-efficacy levels related to Sudden Infant Death Syndrome (SIDS).
Who can participate
Age range18 Years – 65 Years
SexFEMALE
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Inclusion Criteria:
* Mothers with a healthy newborn baby,
* Mothers who have not experienced any previous child loss,
* Mothers with at least a primary school education,
* Mothers who own a smartphone with mobile internet access,
* Mothers who speak Turkish, are able to understand written and spoken information, follow instructions, and have no communication barriers,
* Mothers who voluntarily agree to participate in the study.
Exclusion Criteria:
* Mothers with postpartum depression,
* Mothers who do not complete the educational program within 15 days,
* Mothers who request withdrawal from the study at any stage.
What they're measuring
1
Knowledge
Timeframe: baseline (first assessment)
2
Knowledge
Timeframe: 2 weeks after from baseline
3
Knowledge
Timeframe: at the end of the invervention program (4 weeks after from baseline)
4
Care Skills
Timeframe: baseline (first assessment)
5
Care Skills
Timeframe: 2 weeks after from baseline
6
Care Skills
Timeframe: at the end of the invervention program (4 weeks after from baseline)