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Published in: BMC Psychiatry 1/2015

Open Access 01-12-2015 | Study protocol

Cost-effectiveness of blended vs. face-to-face cognitive behavioural therapy for severe anxiety disorders: study protocol of a randomized controlled trial

Authors: Geke Romijn, Heleen Riper, Robin Kok, Tara Donker, Maartje Goorden, Leona Hakkaart van Roijen, Lisa Kooistra, Anton van Balkom, Jeroen Koning

Published in: BMC Psychiatry | Issue 1/2015

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Abstract

Background

Anxiety disorders are among the most prevalent psychiatric conditions, and are associated with poor quality of life and substantial economic burden. Cognitive behavioural therapy is an effective treatment to reduce anxiety symptoms, but is also costly and labour intensive. Cost-effectiveness could possibly be improved by delivering cognitive behavioural therapy in a blended format, where face-to-face sessions are partially replaced by online sessions. The aim of this trial is to determine the cost-effectiveness of blended cognitive behavioural therapy for adults with anxiety disorders, i.e. panic disorder, social phobia or generalized anxiety disorder, in specialized mental health care settings compared to face-to-face cognitive behavioural therapy. In this paper, we present the study protocol. It is hypothesized that blended cognitive behavioural therapy for anxiety disorders is clinically as effective as face-to-face cognitive behavioural therapy, but that intervention costs may be reduced. We thus hypothesize that blended cognitive behavioural therapy is more cost-effective than face-to-face cognitive behavioural therapy.

Methods/design

In a randomised controlled equivalence trial 156 patients will be included (n = 78 in blended cognitive behavioural therapy, n = 78 in face-to-face cognitive behavioural therapy) based on a power of 0.80, calculated by using a formula to estimate the power of a cost-effectiveness analysis: \( n=\frac{2{\left({z}_a+{z}_{\beta}\right)}^2\left(s{d}^2+\left({W}^2s{d}^2\right)-\left(2W\rho s{d}_cs{d}_q\right)\right)}{{\left( WE-C\right)}^2} \). Measurements will take place at baseline, midway treatment (7 weeks), immediately after treatment (15 weeks) and 12-month follow-up. At baseline a diagnostic interview will be administered. Primary clinical outcomes are changes in anxiety symptom severity as measured with the Beck Anxiety Inventory. An incremental cost-effectiveness ratio will be calculated to obtain the costs per quality-adjusted life years (QALYs) measured by the EQ-5D (5-level version). Health-economic outcomes will be explored from a societal and health care perspective.

Discussion

This trial will be one of the first to provide information on the cost-effectiveness of blended cognitive behavioural therapy for anxiety disorders in routine specialized mental health care settings, both from a societal and a health care perspective.

Trial registration

Netherlands Trial Register NTR4912. Registered 13 November 2014.
Appendix
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Metadata
Title
Cost-effectiveness of blended vs. face-to-face cognitive behavioural therapy for severe anxiety disorders: study protocol of a randomized controlled trial
Authors
Geke Romijn
Heleen Riper
Robin Kok
Tara Donker
Maartje Goorden
Leona Hakkaart van Roijen
Lisa Kooistra
Anton van Balkom
Jeroen Koning
Publication date
01-12-2015
Publisher
BioMed Central
Published in
BMC Psychiatry / Issue 1/2015
Electronic ISSN: 1471-244X
DOI
https://doi.org/10.1186/s12888-015-0697-1

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