The Half Swaddling Application on Infant Sleep Routine, Maternal Sleep Quality, Depression
Recruiting · NCT06750796 · Interventional (participants receive a specific treatment) · Lead sponsor: Tanta University
View the official record on ClinicalTrials.gov →Interventions studied
The Half Swaddling Application
What this trial is about
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.
Who can take part
Age range
18 Years to 45 Years
Sex
Female
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- 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.
Exclusion criteria
- 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
1 location listed.
- Trakya University - Edirne, None Selected, Turkey (Türkiye)