Ignite Creation Date:
2024-05-19 @ 5:34 PM
Last Modification Date:
2024-10-26 @ 3:29 PM
Study NCT ID:
NCT06413784
Status:
COMPLETED
Last Update Posted:
2024-05-14
First Post:
2024-05-09
Brief Title:
Examining The Effect of Chronotype Differences on Sleep Quality and Pregnancy Symptoms in Pregnant Women
Sponsor:
Istanbul Medipol University Hospital
Organization:
Istanbul Medipol University Hospital
Study Overview
Official Title:
Examining The Effect of Chronotype Differences on Sleep Quality and Pregnancy Symptoms in Pregnant Women
Status:
COMPLETED
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Purpose The aim of this study was to examine the effect of chronotype differences on sleep quality and pregnancy symptoms in pregnant women
Methods Eighty-five pregnant women in the second trimester were included in the study The chronotypes of pregnant women were determined using the Morningness-Eveningness Questionnaire MEQ Then Oral Glucose Tolerance tests were performed on the participants between 24-28 weeks Also pregnant womens nausea and vomiting conditions with the Pregnancy-Unique Quantification of Emesis and Nausea PUQE and sleep quality with Pittsburgh Sleep Quality Index PSQI were evaluated
Methods Eighty-five pregnant women in the second trimester were included in the study The chronotypes of pregnant women were determined using the Morningness-Eveningness Questionnaire MEQ Then Oral Glucose Tolerance tests were performed on the participants between 24-28 weeks Also pregnant womens nausea and vomiting conditions with the Pregnancy-Unique Quantification of Emesis and Nausea PUQE and sleep quality with Pittsburgh Sleep Quality Index PSQI were evaluated
Detailed Description:
Purpose The aim of this study was to examine the effect of chronotype differences on sleep quality and pregnancy symptoms in pregnant women
Methods This study is a single-blind participants parallel trial It was performed in line with the principles of the Declaration of Helsinki The followings were the studys inclusion requirements being between the ages of 18-40 having a singleton pregnancy being in the second trimester and not having any known chronic disease Exclusion criteria are working night shifts having a high-risk pregnancy and having a neurological or orthopedic disease Eighty-five pregnant women in the second trimester were included in the study The chronotypes of pregnant women were determined using the Morningness-Eveningness Questionnaire MEQ Then Oral Glucose Tolerance tests were performed on the participants between 24-28 weeks Also pregnant womens nausea and vomiting conditions with the Pregnancy-Unique Quantification of Emesis and Nausea PUQE and sleep quality with Pittsburgh Sleep Quality Index PSQI were evaluated
Methods This study is a single-blind participants parallel trial It was performed in line with the principles of the Declaration of Helsinki The followings were the studys inclusion requirements being between the ages of 18-40 having a singleton pregnancy being in the second trimester and not having any known chronic disease Exclusion criteria are working night shifts having a high-risk pregnancy and having a neurological or orthopedic disease Eighty-five pregnant women in the second trimester were included in the study The chronotypes of pregnant women were determined using the Morningness-Eveningness Questionnaire MEQ Then Oral Glucose Tolerance tests were performed on the participants between 24-28 weeks Also pregnant womens nausea and vomiting conditions with the Pregnancy-Unique Quantification of Emesis and Nausea PUQE and sleep quality with Pittsburgh Sleep Quality Index PSQI were evaluated
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None