Short-term Neonatal and Parental Outcomes in Low- and High-Risk Infants (NCT07534748) | Clinical Trial Compass
CompletedNot Applicable
Short-term Neonatal and Parental Outcomes in Low- and High-Risk Infants
Turkey (Türkiye)34 participantsStarted 2024-01-01
Plain-language summary
This study aimed to evaluate the short-term neonatal and parental outcomes in low- and high-risk infants following a single-session family care education intervention. A total of 34 parent-infant dyads were included.
All parents received a structured, family care education during hospitalization. Parental depression, anxiety, care participation, and neonatal pain were assessed on the 10th day of hospitalization and at discharge.
Who can participate
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
* Infants diagnosed as neurodevelopmentally at risk.
* Infants born between 37 and 40 gestational weeks.
* Infants with a birth weight below 2500 grams.
* Infants who have been admitted to the neonatal intensive care unit for at least 10 days since birth.
Exclusion Criteria:
* Infants whose families declined participation in the study.
* Infants with congenital anomalies.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This study looked at both 'low-risk' and 'high-risk' infants — can you help me understand which category my baby would have fallen into, and what that means for how I should interpret the findings?
2The trial measured parental participation in care alongside outcomes like postnatal depression and anxiety — did the results suggest that how involved parents are in their baby's care actually made a difference to those mental health scores?
3Since neonatal pain was one of the main things being tracked, what did this study find about how pain in newborns connects to parent wellbeing, and does that change anything about how you manage pain for babies in our situation?
4Now that this trial is completed, are the findings published somewhere I can read them, and do you think the results are strong enough to influence how you'd approach my baby's care or my own mental health support?
5Given that this was a non-interventional observational study with no assigned phase, does that mean it was mainly gathering information rather than testing a treatment — and if so, how does it help inform what actual care options are available to us?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.