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Clinical Trials in Germany / NCT06627140
Recruiting Observational

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

NCT06627140 · tracked via the Priya Life Science Germany tracker
Phase
Observational
Started
2024-07-08
Last updated
2024-10-04

Condition(s) studied

Preterm BirthPsychological DistressMental HealthCognitive Functioning

Investigational drug(s) / intervention(s)

Diagnostic procedures

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

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.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
Accepted
Children and their parents must have participated in the previous study. Inclusion criteria of the previous study regarding the parents were: * Pregnant women and their partners from the 24th week of gestation on * 18 years of age Exclusion criteria of the previous study were: * Psychiatric, mainly psychotic diseases * Drug abuse * Severe neurological disorders * Stillbirth

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Johann Wolfgang Goethe University Frankfurt am Main Hesse Recruiting

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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 NCT06627140 on ClinicalTrials.gov ↗ ← All trials in Germany