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Effectiveness and cost-effectiveness of a fully self-guided internet-based intervention for sub-clinical social anxiety symptoms: Protocol for a randomised controlled trial.
Powell, John; Atherton, Helen; Williams, Veronika; Martin, Angela; Bennett, Kylie; Bennett, Anthony; Mollison, Jill; Yu, Ly-Mee; Yang, Yaling; Locock, Louise; Davoudianfar, Mina; Griffiths, Kathleen M.
Afiliação
  • Powell J; Nuffield Department of Primary Care Health Sciences, University of Oxford, UK.
  • Atherton H; Warwick Medical School, University of Warwick, UK.
  • Williams V; Nuffield Department of Primary Care Health Sciences, University of Oxford, UK.
  • Martin A; Nuffield Department of Primary Care Health Sciences, University of Oxford, UK.
  • Bennett K; National Institute for Mental Health Research, Australian National University, Australia.
  • Bennett A; National Institute for Mental Health Research, Australian National University, Australia.
  • Mollison J; Nuffield Department of Primary Care Health Sciences, University of Oxford, UK.
  • Yu LM; Nuffield Department of Primary Care Health Sciences, University of Oxford, UK.
  • Yang Y; Nuffield Department of Primary Care Health Sciences, University of Oxford, UK.
  • Locock L; Nuffield Department of Primary Care Health Sciences, University of Oxford, UK.
  • Davoudianfar M; Nuffield Department of Primary Care Health Sciences, University of Oxford, UK.
  • Griffiths KM; National Institute for Mental Health Research, Australian National University, Australia.
Digit Health ; 3: 2055207617702272, 2017.
Article em En | MEDLINE | ID: mdl-29942591
ABSTRACT
DESIGN AND

OBJECTIVE:

This paper describes the protocol for a large-scale pragmatic, randomised controlled trial and economic evaluation to investigate the effectiveness and cost-effectiveness of the self-directed E-Couch social anxiety module versus a waiting list control condition, for reducing sub-clinical social anxiety symptoms in the general population. STUDY POPULATION Community-based adults (aged 18+) with social anxiety symptoms that do not meet the criteria for social anxiety disorder recruited via a direct-to-consumer advertisement on national websites. INTERVENTION AND CONTROL Intervention is the self-guided E-Couch social anxiety module. Control group participants are placed on a waiting list to receive the intervention at the end of the trial. Both groups receive email and text message reminders. OUTCOME

MEASURES:

The primary outcome will be change in self-reported social anxiety score using the Social Phobia Inventory (SPIN). Secondary outcomes will be the changes in the following self-report

measures:

Brief Fear of Negative Evaluation scale (BFNE-S); depression (CES-D); mental wellbeing (SWEMWEBS); health status (SF36); use of health services; safety events; and adherence, retention, and attrition rates. All measures will be administered at baseline, 6 weeks, and 3, 6 and 12 months.

ANALYSIS:

A mixed effects model will be used to analyse the effect of the intervention on the primary and secondary outcomes (intention to treat analysis). Secondary analyses will explore moderators and mediators of effect. A prospective economic evaluation, conducted from a NHS and social care perspective, will provide estimates of cost utility and cost-effectiveness. An interview study will be conducted with 20 participants to explore issues including acceptability, adherence, retention and attrition. TRIAL REGISTRATION NUMBERS NCT02451878 and ISRCTN15819951.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Health_economic_evaluation / Prognostic_studies / Qualitative_research Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Health_economic_evaluation / Prognostic_studies / Qualitative_research Idioma: En Ano de publicação: 2017 Tipo de documento: Article