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タイトル: Relapse prevention group therapy via video-conferencing for substance use disorder: protocol for a multicentre randomised controlled trial in Indonesia
著者: Yamada, Chika  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-6288-5532 (unconfirmed)
Siste, Kristiana
Hanafi, Enjeline
Ophinni, Youdiil  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0001-9443-1538 (unconfirmed)
Beatrice, Evania
Rafelia, Vania
Alison, Peter
Limawan, Albert
Shinozaki, Tomohiro
Matsumoto, Toshihiko
Sakamoto, Ryota  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-0774-9925 (unconfirmed)
著者名の別形: 山田, 千佳
坂本, 龍太
発行日: Sep-2021
出版者: BMJ
誌名: BMJ Open
巻: 11
号: 9
論文番号: e050259
抄録: [Background] Substance use disorder (SUD) is a leading contributor to the global burden of disease. In Indonesia, the availability of formal treatment for SUD falls short of the targeted coverage. A standardised therapeutic option for SUD with potential for widespread implementation is required, yet evidence-based data in the country are scarce. In this study, we developed a cognitive behavioural therapy (CBT)-based group telemedicine model and will investigate effectiveness and implementability in a multicentre randomised controlled trial. [Methods] A total of 220 participants will be recruited from the social networks of eight sites in Indonesia: three hospitals, two primary healthcare centres and three rehabilitation centres. The intervention arm will participate in a relapse prevention programme called the Indonesia Drug Addiction Relapse Prevention Programme (Indo-DARPP), a newly developed 12-week module based on CBT and motivational interviewing constructed in the Indonesian context. The programme will be delivered by a healthcare provider and a peer counsellor in a group therapy setting via video-conferencing, as a supplement to participants’ usual treatments. The control arm will continue treatment as usual. The primary outcome will be the percentage increase in days of abstinence from the primarily used substance in the past 28 days. Secondary outcomes will include addiction severity, quality of life, motivation to change, psychiatric symptoms, cognitive function, coping, and internalised stigma. Assessments will be performed at baseline (week 0), post-treatment (week 13), and 3 and 12 months post-treatment completion (weeks 24 and 60). Retention, participant satisfaction, and cost-effectiveness will be assessed as the implementation outcomes. [Ethics and dissemination] The study protocol was reviewed and approved by the Ethics Committees of Universitas Indonesia and Kyoto University. The results will be disseminated via academic journals and international conferences. Depending on trial outcomes, the treatment programme will be advocated for adoption as a formal healthcare-based approach for SUD.
著作権等: © Author(s) (or their employer(s)) 2021.
This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial.
URI: http://hdl.handle.net/2433/270385
DOI(出版社版): 10.1136/bmjopen-2021-050259
PubMed ID: 34489288
出現コレクション:学術雑誌掲載論文等

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