Clinical trial for Infant, Newborn
Official title The Half Swaddling Application on Infant Sleep Routine, Maternal Sleep Quality, Depression
ClinicalTrials.gov ID: NCT06750796
What this study is testing
- What it's testing
- 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.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 45, women only. Healthy volunteers may be eligible.
You may be able to join 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,
You likely can't join 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,
See the full eligibility 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.
- 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.
The study team makes the final eligibility decision.
Where it's taking place
- Edirne, None Selected, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 18 years to 45 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Edirne, None Selected, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.