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Child and Adolescent Psychiatric Personality Structure

NCT05162287 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 62

Last updated 2023-07-19

No results posted yet for this study

Summary

The study plan outlined here represents an investigation of instruments on the patients treated in the acute ward of child and adolescent psychiatry at the University Medical Center Hamburg Eppendorf (UKE). The psychosocial burden of the affected children and adolescents is evident due to the severity of the disorders leading to specific admission. The psychosocial burden can be defined as "psychological, social, or school-occupational functional impairment \[...\] that has arisen as a consequence of a mental disorder, a specific developmental disorder, or an intellectual impairment". The current research project aims to survey the severity of psychosocial distress, personality functioning impairment, and social withdrawal. A better knowledge of these factors may contribute to a more suitable, specialized treatment offer on the acute ward in the medium term.

Conditions

  • Personality Disorders
  • Social Withdrawal of Childhood or Adolescence
  • Psychosocial Impairment

Sponsors & Collaborators

  • Universitätsklinikum Hamburg-Eppendorf

    lead OTHER

Principal Investigators

  • Johannes Boettcher, M.Sc. · Department of Child and Adolescent Psychiatry, Psychotherapy and Psychosomatics

  • Carola Bindt, PD Dr. · Department of Child and Adolescent Psychiatry, Psychotherapy and Psychosomatics

  • Ursula Völker, Dr. · Department of Child and Adolescent Psychiatry, Psychotherapy and Psychosomatics

Eligibility

Min Age
12 Years
Max Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-12-01
Primary Completion
2022-12-01
Completion
2022-12-05

Countries

  • Germany

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 NCT05162287 on ClinicalTrials.gov