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Suicide prevention of women of Turkish origin in Berlin [Suizidprävention bei Berliner Frauen mit türkischem Migrationshintergrund]
ISRCTN ISRCTN96382348
ClinicalTrials.gov identifier
Public title Suicide prevention of women of Turkish origin in Berlin [Suizidprävention bei Berliner Frauen mit türkischem Migrationshintergrund]
Scientific title Suicide attempt rates and suicide prevention of women of Turkish origin in Berlin [Suizidversuchsraten und Suizidprävention bei Berliner Frauen mit türkischem Migrationshintergrund]
Acronym SPIMig
Serial number at source 01EL0807
Study hypothesis Studies demonstrate that suicidality in female Turkish immigrants in some European countries is higher compared to native-born women of the same age. This indicates a demand for a better understanding of suicide in this group of the society, and, based on such knowledge, specific concepts for prevention.

Through a population-based multi-modal intervention project:
1. Suicide attempt rates can be reduced
2. The mental health service use of the target population will be increased
Lay summary Not provided at time of registration
Ethics approval Ethics Committee of Charite - University Medicine Berlin approved on the 30th June 2009 (ref: EA1/177/08)
Study design Repeat cross-sectional controlled trial with a quasi-experimental design
Countries of recruitment Germany
Disease/condition/study domain Suicide attempts
Participants - inclusion criteria 1. Women aged 18 years or older
2. City of residence in one of the study centres (Berlin, Hamburg)
3. Turkish migration background (including: 1st, 2nd and 3rd generation)
Participants - exclusion criteria Does not meet inclusion criteria
Anticipated start date 01/07/2009
Anticipated end date 30/09/2011
Status of trial Completed
Patient information material Not available in web format, please use the contact details below to request a patient information sheet
Target number of participants 132,500 (target population in Berlin)
Interventions In the intervention region (Berlin):
1. Public awareness campaign (duration: 6 months)
2. Telephone hotline in Turkish language for women in emotional crisis (duration: 9 months)
3. Training of key persons. These include teachers, social workers, general practitioners, health workers who are working with the target population (duaration: 6 months).

In the control region (Hamburg):
No intervention will take place.

Scientific contact details:
Principal investigator:
Prof. Dr. med. Andreas Heinz
Department of Psychiatry and Psychotherapy
Charité - Universitätsmedizin Berlin
Campus Charité Mitte
Charitéplatz 1
10117 Berlin
Germany
Primary outcome measure(s) Presentation of a suicide attempts in the target population in one of the participating emergency rooms:
1. The diagnosis is based on the clinical evaluation of a physician
2. Suicide attempts are classified according to International Classification of Diseases (ICD-10) criteria
Secondary outcome measure(s) In the population-based survey:
1. Changes in information about psychiatric health care services
2. Changes in mental health service use
Sources of funding 1. Federal Ministry for Education and Research (Bundeministerium für Bildung und Forschung [BMBF]) (Germany) (ref: 01EL0807)
2. Charité - University Medicine Berlin (Charité - Universitätsmedizin Berlin) (Germany)
3. University Medical Center Hamburg-Eppendorf (Germany)
Trial website
Publications
Contact name Prof  Andreas  Heinz
  Address Department of Psychiatry and Psychotherapy Charité
Universitätsmedizin Berlin, Campus Charité Mitte
Charitéplatz 1
  City/town Berlin
  Zip/Postcode 10117
  Country Germany
Sponsor German Centre for Aerospace (Deutsches Zentrum fur Luft- und Raumfahrt e.V.) (Germany)
  Address Heinrich-Konen-Strasse 1
  City/town Bonn
  Zip/Postcode 53227
  Country Germany
  Sponsor website: http://www.dlr.de/
Date applied 04/11/2010
Last edited 21/11/2011
Date ISRCTN assigned 18/11/2011
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