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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
来源:
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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