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Clinical Trials in Turkey / NCT06750796
Recruiting Not applicable

The Half Swaddling Application on Infant Sleep Routine, Maternal Sleep Quality, Depression

NCT06750796 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2023-05-18
Last updated
2024-12-27

Condition(s) studied

Infant, NewbornMaternal Outcome

Investigational drug(s) / intervention(s)

The Half Swaddling Application

The Half Swaddling Application: Half swaddling application in term babies

Study summary

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.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
45 Years
Healthy volunteers
Accepted
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.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Trakya University Edirne None Selected Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06750796 on ClinicalTrials.gov ↗ ← All trials in Turkey