Translated and culturally adapted internet-delivered cognitive therapy for social anxiety disorder in Japanese clinical settings: study protocol for a randomised controlled trial

被引:0
|
作者
Yoshinaga, Naoki [1 ]
Thew, Graham R. [2 ,3 ]
Hayashi, Yuta [4 ]
Tanoue, Hiroki [1 ]
Nakai, Michikazu [5 ,6 ]
Clark, David M. [2 ]
机构
[1] Univ Miyazaki, Fac Med, Sch Nursing, 5200 Kihara, Miyazaki City 8891692, Japan
[2] Univ Oxford, Dept Expt Psychol, Paradise Sq, Oxford OX1 1TW, England
[3] Oxford Hlth NHS Fdn Trust, Oxford, England
[4] Kobe Univ, Grad Sch Hlth Sci, Dept Nursing, 7-10-2 Tomogaoka,Suma Ku, Kobe, Hyogo 6540142, Japan
[5] Univ Miyazaki, Fac Med, Dept Social Med, Div Data Management, 5200 Kihara, Miyazaki City 8891692, Japan
[6] Univ Miyazaki, Univ Miyazaki Hosp, Fac Med, Clin Res Support Ctr, 5200 Kihara, Miyazaki City 8891692, Japan
基金
日本学术振兴会;
关键词
Clinical trial protocol; Cognitive behavioural therapy; Cognitive therapy; Cultural adaptation; Internet interventions; Japan; Randomised controlled trial; Social anxiety disorder; SCALE; VALIDITY;
D O I
10.1186/s13063-024-08303-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundCognitive therapy for social anxiety disorder (CT-SAD) has extensive empirical support and is recommended in several national guidelines. However, ensuring access to evidence-based psychological therapies such as CT-SAD remains a global challenge. An internet-delivered version of this treatment protocol (iCT-SAD) has recently been developed in the UK as a way to overcome this challenge, demonstrating comparable outcomes to face-to-face CT-SAD whilst requiring less therapist time per client. Initial findings also suggest its cross-cultural transferability, but the previous studies in other cultural settings used the English language programme and only included English-fluent participants as a second language. It is not yet known what outcomes can be achieved once the programme has been translated and adapted for a different cultural context. Therefore, this trial aims to evaluate the clinical efficacy of Japanese iCT-SAD when combined with treatment as usual (TAU) in clients with SAD.MethodsThis two-arm, parallel-group, superiority randomised controlled trial will recruit 60 Japanese participants with SAD, randomly assigning them to either Japanese iCT-SAD + TAU or TAU alone at a ratio of 1:1. The primary outcome measure is the self-report Liebowitz Social Anxiety Scale, and secondary.outcomes include other measures of social anxiety symptoms and processes, general mood and functioning, and response to treatment. We will also assess treatment acceptability and gather participant feedback. Assessments will take place at baseline (week 0), mid-treatment (week 8), and post-treatment (week 15), with a further 3-month follow-up (week 27) for the iCT-SAD + TAU arm. The primary analyses will be conducted on an intent-to-treat basis, comparing the primary and secondary outcome measures between groups using linear mixed-effect models, along with additional mediation analysis.DiscussionInvestigating the efficacy of translated and culturally adapted iCT-SAD in different cultural contexts is an important step in evaluating the global reach of internet interventions. This trial will provide valuable insights into the effects of iCT-SAD combined with usual care, and how this treatment could be delivered in routine clinical settings in Japan.Trial registrationInternational Standard Randomized Controlled Trials (ISRCTN), ISRCTN82859645, registered on January 19, 2024. UMIN Clinical Trials Registry (UMIN-CTR), UMIN000052702, registered on November 6, 2023.
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页数:12
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