COTEPS: Monitoring of Incidence of Mental Discomfort in Pregnant Women During the Serious COVID-19 Pandemic Conditions

Sponsor
Comenius University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04898192
Collaborator
(none)
1,500
1
16
93.8

Study Details

Study Description

Brief Summary

This study is aimed to detect severe fear of delivery and its association with the incidence of obsessive-compulsive disorder and symptoms of depression and anxiety in the population of pregnant women in the third trimester during the serious COVID-19 pandemic situation in Slovakia. Data will be acquired from three departments of gynaecology and obstetrics of University Hospital Bratislava. The majority of pregnancies from the region are managed in this hospital; the total number of deliveries in 2020 achieved 7,835

Condition or Disease Intervention/Treatment Phase
  • Other: questionnaire

Detailed Description

The pregnancy is a risk factor for the first manifestation of several mental disorders. Current serious pandemic situation and a constant risk of COVID-19 infection negatively affects the mental state of the population, risk groups of pregnant women in particular. The aim of this project is to discover the incidence of symptoms of depression, anxiety and obsessive-compulsive disorder in association with the fear of delivery in current COVID-19 pandemic conditions in Slovakia. We also decided to add a short tool for detection of domestic violence among other scales to detect the incidence among Slovak pregnant population. All pregnant women in their third trimester who visit the prenatal clinic for their routine weekly check-up will be asked to participate in the study. The questionnaire which comprises of validated mental scales will be handed out to the patients waiting for their examination. After collection of filled questionnaires, those will be later paired with patients' medical documentation and statistically evaluated. The questionnaires will be collected during the period of 1.4.2021-31.3.2022 and statistical analysis will be conducted in the period of 1.4.2022-1.8.2022. It is expected that approximately 1,500 women will be included into the study. All three departments of gynaecology and obstetrics of the University Hospital Bratislava will participate at the study. In total, approximately 7,800 deliveries a year are managed in the University Hospital Bratislava.

Following questionnaires are planned to be used in the study:
  • Wijma Delivery Expectancy/Experience Questionnaire - aimed at fear of delivery

  • PASS (Perinatal Anxiety Screening Scale) - aimed at anxiety in women before and after delivery

  • PHQ-9-SK (Patient Health Questionnaire) - aimed at depressive disorder

  • HITS Domestic Violence Screening Tool - aimed at domestic violence

  • DOK (The Obsessive-Compulsive Inventory) - aimed at obsessive and compulsive symptoms

  • GAD-7 (General Anxiety Disorder-7) - aimed at general anxiety disorder

  • EPDS (Edinburgh Postnatal Depression Scale) - aimed at symptoms of postpartal depression

Study Design

Study Type:
Observational
Anticipated Enrollment :
1500 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
COTEPS: Monitoring of Incidence of Mental Discomfort in the Population of Pregnant Women in the Third Trimester During the Serious COVID-19 Pandemic Conditions
Actual Study Start Date :
Apr 1, 2021
Anticipated Primary Completion Date :
Mar 31, 2022
Anticipated Study Completion Date :
Aug 1, 2022

Outcome Measures

Primary Outcome Measures

  1. prevalence and risk factors [9 months]

    prevalence and risk factors of depression, anxiety and obsessive-compulsive disorder in the population of pregnant women in association with COVID-19 pandemic situation.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Pregnancy after 34th week

  • Vital fetus

Exclusion Criteria:
  • Unwilling to participate

  • Age less than 18 years

  • Foetus mortus or perinatal death of the newborn

  • Low knowledge of Slovak language

  • Serious pathology in the pregnancy (e.g. placenta praevia, known congenital disorders)

Contacts and Locations

Locations

Site City State Country Postal Code
1 2nd Department of Obstetrics and Gynecology, University Hospital Bratislava and Comenius University, Bratislava, Slovak Republic Bratislava Slovensko Slovakia 83232

Sponsors and Collaborators

  • Comenius University

Investigators

  • Study Chair: Jozef Zahumensky, prof. MD, Comenius University in Bratislava

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Peter Musil, head of project centre Faculty of Medicine, Comenius University
ClinicalTrials.gov Identifier:
NCT04898192
Other Study ID Numbers:
  • EC/045/2021/UNBRuzinov
First Posted:
May 24, 2021
Last Update Posted:
May 26, 2021
Last Verified:
May 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Peter Musil, head of project centre Faculty of Medicine, Comenius University
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 26, 2021