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Internet-delivered cognitive therapy for social anxiety disorder in Hong Kong: A randomized controlled trial.
Thew, Graham R; Kwok, Amy P L; Lissillour Chan, Mandy H; Powell, Candice L Y M; Wild, Jennifer; Leung, Patrick W L; Clark, David M.
Afiliación
  • Thew GR; Department of Experimental Psychology, University of Oxford, UK.
  • Kwok APL; Oxford University Hospitals NHS Foundation Trust, UK.
  • Lissillour Chan MH; Oxford Health NHS Foundation Trust, UK.
  • Powell CLYM; Hong Kong East Cluster, Hospital Authority, Hong Kong, China.
  • Wild J; Hong Kong East Cluster, Hospital Authority, Hong Kong, China.
  • Leung PWL; New Life Psychiatric Rehabilitation Association, Hong Kong, China.
  • Clark DM; Department of Experimental Psychology, University of Oxford, UK.
Internet Interv ; 28: 100539, 2022 Apr.
Article en En | MEDLINE | ID: mdl-35493437
Background: Research is needed to determine the extent to which internet-delivered psychological therapies are effective when delivered in countries and cultures outside of where they were developed. Objective: This waitlist-controlled study evaluated the efficacy of a UK-developed, therapist-guided internet Cognitive Therapy programme for Social Anxiety Disorder (iCT-SAD) when delivered in Hong Kong by local therapists. Methods: Patients were randomized to iCT-SAD (n = 22) or a waitlist control group (n = 22). Assessments took place at weeks 0, 8, and 15 (posttreatment/postwait), with a further 3-month follow-up assessment for the iCT-SAD group. The primary outcome measure was the Liebowitz Social Anxiety Scale (self-report), and posttreatment/postwait diagnostic assessments were completed by independent assessors blind to condition. Trial Registration: ISRCTN11357117. Results: Compared with the waitlist group, iCT-SAD significantly reduced social anxiety symptoms (adjusted difference at posttreatment 55.36, 95%CI 44.32 to 66.39, p < 0.001; d Cohen 2.41). The treatment was also superior to waitlist on all secondary outcome measures. 86% of the iCT-SAD group demonstrated remission from SAD based on the LSAS, compared to 5% of the waitlist group. 73% no longer met diagnostic criteria at posttreatment, compared to 9% of the waitlist group. The gains made by the iCT-SAD group were maintained at three-month follow-up. Conclusions: iCT-SAD showed strong efficacy for the treatment of SAD in Hong Kong. As the clinical outcomes were similar to UK studies, this suggests the dissemination of the treatment into a different cultural setting did not result in a substantial loss of efficacy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Internet Interv Año: 2022 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Internet Interv Año: 2022 Tipo del documento: Article Pais de publicación: Países Bajos