Expected and Actual Preterm-Birth and Parental Distress: Impact on Children's Mental Health

NCT06627140 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 250

Last updated 2024-10-04

No results posted yet for this study

Summary

The purpose of the present study is the assessment of the mental health and cognitive development of children 6-11 years after premature or term birth. Impairments in children's' mental health are assessed focusing different disorders or problems (ADHD, Autism traits, Affective disorders, oppositional-aggressive behavior) and using both questionnaires and a clinical interview. Risk and protective factors will be analyzed, e.g., threat and/or actual premature birth compared to term birth, parents' mental health, positive coping, personality traits and social support in the peripartum period and afterwards, as well as medical parameters. The potential interaction of premature birth, medical complications, parental distress and children's mental health will be taken into consideration.

Conditions

Interventions

DIAGNOSTIC_TEST

Diagnostic procedures

Self- and parent-report on behavioral/emotional symptoms and assessment of cognitive functioning

Sponsors & Collaborators

  • Johann Wolfgang Goethe University Hospital

    collaborator OTHER
  • Goethe University

    lead OTHER

Principal Investigators

  • Katharina Szota, PhD · Johann Wolfgang Goethe University, Philipps-University Marburg

  • Susan Schwarz, PhD · Goethe University

  • Silvia Oddo-Sommerfeld, PhD · Johann Wolfgang Goethe University Hospital

  • Frank Louwen, Prof · Johann Wolfgang Goethe University Hospital

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-07-08
Primary Completion
2024-10-31
Completion
2024-12-20

Countries

  • Germany

Study Locations

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Entities

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 NCT06627140 on ClinicalTrials.gov