The Half Swaddling Application on Infant Sleep Routine, Maternal Sleep Quality, Depression
Recruiting now · Not applicable
Conditions studied: Infant, Newborn, Maternal Outcome
In brief
In this prospective controlled study, it was aimed to examine the effects of half swaddling in term infants on infant sleep routine, maternal sleep quality and postpartum depression.
Key facts
- Study ID
- NCT06750796
- Run by
- Tanta University
- People needed
- 128
- Starts
- 2023-05-18
- Expected to finish
- 2025-12-15
- Last updated by the study team
- 2024-12-27
Who can join
Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- 18-45 years old,
- Term birth (single birth over 37 weeks),
- After an uncomplicated pregnancy process, the delivery was completed by normal vaginal or cesarean delivery method,
- Not using cigarettes, alcohol and stimulants,
- BMI<30,
- Not working on night shift,
- Stable vital signs,
- Those who have not received infertility treatment,
- Do not have a chronic disease (such as hypertension, diabetes mellitus),
- Not experiencing serious depression, anxiety and stress,
- Not having any organic or non-organic disease that can cause cognitive impairment (such as Delirium, Dementia, Intellectual Retardation, etc.),
- No serious maternal complications,
- Mothers who volunteered to participate in the study will be included in the study.
- For baby;
- Birth weight over 2500 g,
- Stable vital signs,
- APGAR score above 7,
- No serious neonatal complications,
- Midwives without congenital malformations will be included in the study.
You may not qualify if…
- under 18 years old,
- Preterm birth (under 37 weeks and/or multiple births),
- Incomplete delivery by normal vaginal or cesarean delivery method after a complicated pregnancy process,
- Using cigarettes, alcohol and stimulants,
- BMI>30,
- Working night shift,
- No stable vital signs,
- Having received infertility treatment,
- Having a chronic disease (such as hypertension, diabetes mellitus),
- Experiencing severe depression, anxiety and stress,
- Having any organic or non-organic disease that can cause cognitive impairment (such as Delirium, Dementia, Intellectual Retardation, etc.),
- Serious maternal complication,
- Mothers who do not volunteer to participate in the study will not be included in the study.
- For baby;
- Birth weight of 2500 g and below,
- No stable vital signs,
- APGAR score below 7,
- Serious neonatal complication,
- Babies with congenital malformations will not be included in the study.
Where it is running
- Trakya University — Edirne, None Selected, Turkey (Türkiye) (enrolling)
Full record on ClinicalTrials.gov
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