Psychiatric Day Hospital Treatment

This study has been completed.
Information provided by:
Technische Universität Dresden Identifier:
First received: September 7, 2005
Last updated: NA
Last verified: September 2005
History: No changes posted
The aim of the study was to compare the effectiveness of acute psychiatric day care to conventional inpatient care within a cross-national multi-site randomised controlled trial.

Condition Intervention
Depressive Disorders
Anxiety Disorders
Personality Disorders
Adjustment Disorders
Behavioral: acute psychiatric day care

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Open Label

Resource links provided by NLM:

Further study details as provided by Technische Universität Dresden:


Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Patients must have presented with a mental disorder with current symptoms that had either led to at least a moderate disturbance in performance in more than one area of daily living or had jeopardized the residential, financial or occupational status of the patient or his family
  • Treatments other than inpatient or day hospital care must have been inadequate or not sufficiently effective for the patient’s current mental state

Exclusion Criteria:

  • Temporary admission for diagnostic purposes or for other reasons
  • Under 18 or over 65 years
  • Admission without consent of the patient (according to country-specific legal regulations)
  • One-way journey to hospital longer than 60 minutes
  • Suicidal risk
  • Risk to others
  • Degree of severity of the disorder requires measures restrictive of the patient's freedom on the day of admission, or a 1:1 supervision, or deems such probable
  • Acute intoxication
  • Main clinical diagnosis: addictive disorder
  • Presence of a somatic disorder requiring inpatient care
  • Direct transfer from a different hospital
  • Homelessness
  • Need for constant pick-up and delivery service
  • Inability to give informed consent with respect to participating in the study
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00153959

Czech Republic
Department of Psychiatry, First Medical Faculty, Charles University of Prague
Prague 2, Czech Republic, 12801
Department of Psychiatry at Dresden University of Technology
Dresden, Saxony, Germany, 01304
Department of Psychiatry, Wroclaw University of Medicine
Wroclaw, Poland, 50-367
Michalovce Psychiatric Hospital
Michalovce, Slovakia, 07101
United Kingdom
Unit for Social and Community Psychiatry, Barts’ and The London School of Medicine
London, United Kingdom, E138 SP
Sponsors and Collaborators
Technische Universität Dresden
Principal Investigator: Thomas W. Kallert, Prof.Dr. Department of Psychiatry at Dresden University of Technology
  More Information

No publications provided Identifier: NCT00153959     History of Changes
Other Study ID Numbers: QLG4-CT-2000-01700
Study First Received: September 7, 2005
Last Updated: September 7, 2005
Health Authority: Germany: Federal Institute for Drugs and Medical Devices

Additional relevant MeSH terms:
Adjustment Disorders
Anxiety Disorders
Depressive Disorder
Personality Disorders
Behavioral Symptoms
Mental Disorders
Mood Disorders
Pathologic Processes processed this record on November 30, 2015