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Pregnancy Without Psychosocial Stress

NCT04853693 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2022-04-11

No results posted yet for this study

Summary

The project is aimed at children who are exposed to the toxic psychosocial stress present in their mothers during pregnancy or after childbirth. Due to psychosocial stress in their mothers, these children are at risk of developing a mental disorder or having impaired psychosocial development.

In Czechia, there is no prevention of psychosocial stress in women, which also plays a preventive role in the development of mental disorders in their children. Mental disorders in parents are stigmatized in Czechia, which prevents parents from seeking care.

The investigators want to change this situation, so they will:

1. create and pilot a screening program for psychosocial stress in perinatal women in gynecological clinics
2. connect the screening program to the integrated step care system created by the investigators, including peer support, which the investigators will test

Conditions

  • Depressive Symptoms
  • Anxiety Disorders and Symptoms
  • Depression, Postpartum

Interventions

BEHAVIORAL

Mom´s Supporting Mom

A preventive peer consultation intervention for Postpartum Depression.

BEHAVIORAL

Enhanced Treatment As Usual

Referral to treatment in the community, clinical monitoring

Sponsors & Collaborators

  • National Institute of Mental Health, Czech Republic

    lead OTHER

Principal Investigators

  • Antonin Sebela, Ph.D. · National Institute of Mental Health, Klecany, Czechia

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-04-01
Primary Completion
2023-03-31
Completion
2023-03-31

Countries

  • Czechia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04853693 on ClinicalTrials.gov