The utility of standardised pre-clinical assessment based on the Development And Well-Being Assessment (DAWBA) in a child and adolescent mental health service

ISRCTN ISRCTN19935149
DOI https://doi.org/10.1186/ISRCTN19935149
Secondary identifying numbers N/A
Submission date
01/08/2007
Registration date
05/09/2007
Last edited
21/03/2013
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Mental and Behavioural Disorders
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

Not provided at time of registration

Contact information

Prof Hans-Christoph Steinhausen
Scientific

Department of Child and Adolescent Psychiatry
University of Zurich
Neumuensterallee 9
POB
Zurich
CH-8032
Switzerland

Phone +41 4349 92730
Email hans-christoph.steinhausen@kjpd.uzh.ch

Study information

Study designRandomised controlled trial
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Not specified
Study typeDiagnostic
Scientific title
Study objectives1. The agreement between pre-clinical assessment (DAWBA based) and blind clinical assessment is incomplete.
2. The disclosure of pre-clinical assessment diagnoses will have an effect on clinical diagnoses including comorbidities.
3. Parents and adolescents will display acceptance and satisfaction with pre-clinical assessment based on the DAWBA.
Ethics approval(s)The trial was approved by the Ethical Committee of the Canton of Zurich, Specialized Subcommittee Psychiatry, Neurology, Neurosurgery, on the 1st June 2007.
Health condition(s) or problem(s) studiedChildhood psychiatric disorders
InterventionThe provision of diagnostic information based on the DAWBA to the clinicians treating the intervention group. The control group will undergo a normal clinical assessment. The diagnostic information will be gathered from parents, adolescents above the age of 11 years, and teachers.
Intervention typeOther
Primary outcome measureThe level of agreement between the pre-clinical assessment and the clinical assessment.
Secondary outcome measuresClinical routine ratings by the clinicians and parents.
Overall study start date01/09/2007
Completion date31/08/2008

Eligibility

Participant type(s)Patient
Age groupChild
Lower age limit5 Years
Upper age limit18 Years
SexBoth
Target number of participants500
Key inclusion criteriaThe trial will include referrals from four outpatient clinics of the service. Patients will be aged 5-18 years.
Key exclusion criteriaChildren of parents with insufficient unterstanding of German and emergency referrals will be excluded.
Date of first enrolment01/09/2007
Date of final enrolment31/08/2008

Locations

Countries of recruitment

  • Switzerland

Study participating centre

Department of Child and Adolescent Psychiatry
Zurich
CH-8032
Switzerland

Sponsor information

University of Zurich (Switzerland)
University/education

Neumuensterallee 9
Postfach
Zurich
CH-8032
Switzerland

Website http://www.uzh.ch/about_en.html
ROR logo "ROR" https://ror.org/02crff812

Funders

Funder type

University/education

Research budget of the Department of Child and Adolescent Psychiatry, University of Zurich (Switzerland)

No information available

Results and Publications

Intention to publish date
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
Publication and dissemination planNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Results article results 01/10/2012 Yes No