International Review of Psychiatry
Volume 27, Issue 1, 2015, Pages 72-81
Protocol: Reducing suicidal ideation among Turkish migrants in the Netherlands and in the UK: Effectiveness of an online intervention (Article)
Eylem O.* ,
Van Straten A. ,
Bhui K. ,
Kerkhof A.J.F.M.
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a
Department of Clinical Psychology, VU University Amsterdam, 1 Van Der Boechorststraat 2B-69, Amsterdam, NL 1081 BT, Netherlands, EMGO Institute for Health and Care Research, Amsterdam, Netherlands, Wolfson Institute of Preventive Medicine, Queen Mary University of London, United Kingdom
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b
Department of Clinical Psychology, VU University Amsterdam, 1 Van Der Boechorststraat 2B-69, Amsterdam, NL 1081 BT, Netherlands, EMGO Institute for Health and Care Research, Amsterdam, Netherlands
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c
Wolfson Institute of Preventive Medicine, Queen Mary University of London, United Kingdom
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d
Department of Clinical Psychology, VU University Amsterdam, 1 Van Der Boechorststraat 2B-69, Amsterdam, NL 1081 BT, Netherlands, EMGO Institute for Health and Care Research, Amsterdam, Netherlands
Abstract
Background: The Turkish community living in Europe has an increased risk for suicidal ideation and attempted suicide. Online self-help may be an effective way of engagement with this community. This study will evaluate the effectiveness of a culturally adapted, guided, cognitive behavioural therapy-based online self-help intervention targeting suicidal ideation for Turkish adults living in the Netherlands and in the UK. Methods and design: This study will be performed in two phases. First, the Dutch online intervention will be adapted to Turkish culture. The second phase will be a randomized controlled trial with two conditions: experimental and waiting-list control. Ethical approval has been granted for the trials in London and Amsterdam. The experimental group will obtain direct access to the intervention, which will take 6 weeks to complete. Participants in the waiting-list condition will obtain access to the modules after 6 weeks. Participants in both conditions will be assessed at baseline, post-test and 3 months post-test follow-up. The primary outcome measure is reduction in frequency and intensity of suicidal thoughts. Secondary outcome measures are self-harm, attempted suicide, suicide ideation attributes, depression, hopelessness, anxiety, quality of life, worrying and satisfaction with the treatment. © 2015 Institute of Psychiatry.
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Link
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84924351886&doi=10.3109%2f09540261.2014.996121&partnerID=40&md5=75cd8742f2c2602c012859ec32e5b46e
DOI: 10.3109/09540261.2014.996121
ISSN: 09540261
Cited by: 3
Original Language: English