Efficacy of digital cognitive behavioural therapy for symptoms of generalised anxiety disorder: a study protocol for a randomised controlled trial

被引:6
|
作者
Gu, J. [1 ,2 ]
Miller, C. B. [1 ,3 ]
Henry, A. L. [1 ,3 ]
Espie, C. A. [1 ,3 ]
Davis, M. L. [1 ]
Stott, R. [1 ,2 ]
Emsley, R. [4 ]
Smits, J. A. J. [5 ]
Craske, M. [6 ]
Saunders, K. E. A. [2 ]
Goodwin, G. [2 ]
Carl, J. R. [1 ]
机构
[1] Big Hlth Inc, San Francisco, CA 94108 USA
[2] Univ Oxford, Dept Psychiat, Oxford, England
[3] Univ Oxford, Sleep & Circadian Neurosci Inst, Nuffield Dept Clin Neurosci, Oxford, England
[4] Kings Coll London, Dept Biostat & Hlth Informat, Inst Psychiat Psychol & Neurosci, London, England
[5] Univ Texas Austin, Dept Psychol, Austin, TX 78712 USA
[6] Univ Calif Los Angeles, Anxiety & Depress Res Ctr ADRC, Los Angeles, CA USA
关键词
Randomised controlled trial; RCT; Digital; Smartphone; Cognitive behavioural therapy; CBT; Generalised anxiety disorder; GAD; Anxiety; QUALITY-OF-LIFE; PSYCHOMETRIC PROPERTIES; SOCIAL ANXIETY; PRIMARY-CARE; SMARTPHONE; PREVALENCE; INTERVENTIONS; METAANALYSIS; COMORBIDITY; PSYCHIATRY;
D O I
10.1186/s13063-020-4230-6
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
Background Generalised anxiety disorder (GAD) is a chronic and disabling condition with considerable personal and economic impact. Cognitive behavioural therapy (CBT) is a recommended psychological therapy for GAD; however, there are substantial barriers to accessing treatment. Digital CBT, in particular smartphone-delivered CBT, has the potential to improve accessibility and increase dissemination of CBT. Despite the emerging evidence of smartphone-based psychological interventions for reducing anxiety, effect size scores are typically smaller than in-person interventions, and there is a lack of research assessing the efficacy of smartphone-delivered digital interventions specifically for GAD. Methods In the DeLTA trial (DigitaL Therapy for Anxiety), we plan to conduct a parallel-group superiority randomised controlled trial examining the efficacy of a novel smartphone-based digital CBT intervention for GAD compared to a waitlist control. We aim to recruit 242 adults (aged 18 years or above) with moderate-to-severe symptoms of GAD. This trial will be conducted entirely online and will involve assessments at baseline (week 0; immediately preceding randomisation), mid-intervention (week 3), post-intervention (week 6; primary end point) and follow-up (week 10). The primary objective is to evaluate the efficacy of the intervention on GAD symptom severity compared to a waitlist control at post-intervention. Secondary objectives are to examine between-group effects on GAD at follow-up, and to examine the following secondary outcomes at both post-intervention and follow-up: 1) worry; 2) depressive symptoms; 3) wellbeing; 4) quality of life; and 5) sleep difficulty. Discussion This trial will report findings on the initial efficacy of a novel digital CBT intervention for GAD. Results have the potential to contribute towards the evidence base for digital CBT for GAD and increase the dissemination of CBT.
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页数:11
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