Dutch Prediction of Psychosis Study

Sponsor
UMC Utrecht (Other)
Overall Status
Unknown status
CT.gov ID
NCT00188981
Collaborator
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) (Other), ZonMw: The Netherlands Organisation for Health Research and Development (Other)
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Study Details

Study Description

Brief Summary

The Dutch Prediction of Psychosis Study (DUPS) is a prospective study of predictors of the transition to psychosis in help-seeking adolescents at high risk for developing a first psychotic episode. The aim of the project is supplemented by a systematic account of the pathways to care, the disabilities and needs and the therapeutic interventions that are currently used in this population.

Multi-level assessment includes behavioral and cognitive variables as well as structural brain imaging and neurophysiological data. Subjects will be followed up at regular intervals during (at least) two years to monitor the development of their (psychotic) symptoms. This will allow us to analyze the predictive validity of the variables.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The Dutch Prediction of Psychosis Study (DUPS) is a collaboration of the Academic Medical Center in Amsterdam (AMC) and the University Medical Center in Utrecht (UMC). The main objectives are:

    1. Pathways to care: the description of the ways subjects at risk for psychosis get access to the health care system and the detection of obstacles to adequate treatment

    2. Prediction: the systematic multi-level assessment of predictors of the transition to a first psychotic episode in subjects at risk for psychosis

    3. Disability: the description of disabilities, deficits and needs in prodromal individuals

    4. Intervention: the description of the therapeutic and preventive interventions applied to prodromal individuals

    While the same fundamental principles (e.g. inclusion criteria) are applied in both centers, additional instruments or paradigms are added in the separate centers according to specific interests, expertise and setting.

    Our specific interest is in the social cognition and social functioning of prepsychotic individuals. Therefore, in addition to the subjects that are at high risk for psychosis according to the DUPS inclusion/exclusion criteria we are including another group of subjects that is at elevated risk for psychosis, namely subjects who have a Multiple Complex Developmental Disorder (MCDD) which is a subtype of the pervasive developmental disorders.

    The study is a prospective longitudinal field-study with repeated measures to monitor subjects at high risk for psychosis.

    The study sample in the UMC consists of adolescents who are already referred to adolescent psychiatric outpatient's clinics because of mental problems. After informed consent they are screened for the following inclusion and exclusion criteria:

    1. Age between 12 and 18 years

    2. No previous psychotic episode for more than one week

    3. Verbal IQ above 75

    4. Symptoms are not due to an organic mental disorder or substance abuse

    5. Belong to one or more of the following groups:

    6. Basic symptoms: presence of self-perceived cognitive thought disturbances

    7. Familial risk plus reduced functioning: having a first- or second degree relative with a history of any psychotic disorder in combination with a deterioration of mental state and/or social functioning in the last year

    8. Attenuated psychotic symptoms: presence of psychotic symptoms at sub-clinical level

    9. Brief, limited or intermittent psychotic symptoms: having a history of psychotic symptoms with a duration of less than one week and spontaneous remission

    10. Multiple Complex Developmental Disorder

    Assessment includes:
    1. basic clinical assessment

    2. neuropsychological measures (attention, memory, executive functioning)

    3. social cognitive measures (facial emotion recognition, mentalizing, social attribution)

    4. measures of social cognition and behavior

    5. EEG and Event Related Potentials (including smooth pursuit eye movement, auditory mismatch negativity)

    6. structural MRI

    Some data will be collected retrospectively upon inclusion into the study, for example symptom history and pathways to care. Outcome is assessed after 9, 18 and 24 months.

    Study Design

    Study Type:
    Observational
    Observational Model:
    Defined Population
    Time Perspective:
    Other
    Official Title:
    Dutch Prediction of Psychosis Study
    Study Start Date :
    Jun 1, 2003
    Anticipated Study Completion Date :
    Jun 1, 2008

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      12 Years to 18 Years
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      Yes
      Inclusion criteria:
      Help-seeking adolescents who belong to one or more of the following groups:
      • Basic symptoms: presence of self-perceived cognitive thought disturbances

      • Familial risk plus reduced functioning: having a first- or second degree relative with a history of any psychotic disorder in combination with a deterioration of mental state and/or social functioning in the last year

      • Attenuated psychotic symptoms: presence of psychotic symptoms at sub-clinical level

      • Brief, limited or intermittent psychotic symptoms: having a history of psychotic symptoms with a duration of less than one week and spontaneous remission

      • Multiple Complex Developmental disorder

      Exclusion criteria:
      • A previous psychotic episode for more than one week

      • Verbal IQ < 75

      • Symptoms are due to an organic mental disorder or substance abuse

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 University Medical Center Utrecht, department of Child and Adolescent Psychiatry Utrecht Netherlands

      Sponsors and Collaborators

      • UMC Utrecht
      • Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
      • ZonMw: The Netherlands Organisation for Health Research and Development

      Investigators

      • Principal Investigator: Patricia Schothorst, PhD, University Medical Center Utrecht, department of Child and Adolescent Psychiatry
      • Principal Investigator: Herman van Engeland, Professor, University Medical Center Utrecht, department of Child and Adolescent Psychiatry

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00188981
      Other Study ID Numbers:
      • CCMOP02.0441C
      • METC02/178
      First Posted:
      Sep 16, 2005
      Last Update Posted:
      Apr 20, 2007
      Last Verified:
      Apr 1, 2007

      Study Results

      No Results Posted as of Apr 20, 2007