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0Phobia – towards a virtual cure for acrophobia: study protocol for a randomized controlled trial

BACKGROUND: Virtual reality exposure therapy (VRET) has been shown to be as effective as traditional forms of in vivo exposure therapy for the treatment of specific phobias. However, as with in vivo exposure, VRET still involves relatively high costs and limited accessibility which makes it prohibit...

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Autores principales: Donker, T., Van Esveld, S., Fischer, N., Van Straten, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085658/
https://www.ncbi.nlm.nih.gov/pubmed/30092844
http://dx.doi.org/10.1186/s13063-018-2704-6
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author Donker, T.
Van Esveld, S.
Fischer, N.
Van Straten, A.
author_facet Donker, T.
Van Esveld, S.
Fischer, N.
Van Straten, A.
author_sort Donker, T.
collection PubMed
description BACKGROUND: Virtual reality exposure therapy (VRET) has been shown to be as effective as traditional forms of in vivo exposure therapy for the treatment of specific phobias. However, as with in vivo exposure, VRET still involves relatively high costs and limited accessibility which makes it prohibitive for a large part of the population. Innovative methods using smartphone applications (apps) may improve accessibility and scalability of VRET. The aim of this study is to evaluate 0Phobia, a gamified self-guided VRET for acrophobia that is delivered through a smartphone app in combination with rudimentary cardboard virtual reality (VR) goggles. METHODS/DESIGN: Participants (N = 180, aged 18–65 years) with acrophobia symptoms will be recruited from the Dutch general population and randomized to either 0Phobia (n = 90) or a waitlist control condition (n = 90). 0Phobia will be delivered over a period of 3 weeks and includes psychoeducation, VR exposure, cognitive techniques, monitoring of symptoms, and relapse prevention. The primary outcome measure will be the Acrophobia Questionnaire. Secondary outcome measures will include user-friendliness, symptoms of anxiety, depression, and mastery. Assessments will take place online at baseline, directly after the intervention (post test) and at follow-up (3 months). DISCUSSION: This study capitalizes on novel technology and recent scientific advances to develop an affordable and scalable treatment modality. TRIAL REGISTRATION: Netherlands Trial Register: NTR6442. Registered on 29 June 2017. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-018-2704-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-60856582018-08-16 0Phobia – towards a virtual cure for acrophobia: study protocol for a randomized controlled trial Donker, T. Van Esveld, S. Fischer, N. Van Straten, A. Trials Study Protocol BACKGROUND: Virtual reality exposure therapy (VRET) has been shown to be as effective as traditional forms of in vivo exposure therapy for the treatment of specific phobias. However, as with in vivo exposure, VRET still involves relatively high costs and limited accessibility which makes it prohibitive for a large part of the population. Innovative methods using smartphone applications (apps) may improve accessibility and scalability of VRET. The aim of this study is to evaluate 0Phobia, a gamified self-guided VRET for acrophobia that is delivered through a smartphone app in combination with rudimentary cardboard virtual reality (VR) goggles. METHODS/DESIGN: Participants (N = 180, aged 18–65 years) with acrophobia symptoms will be recruited from the Dutch general population and randomized to either 0Phobia (n = 90) or a waitlist control condition (n = 90). 0Phobia will be delivered over a period of 3 weeks and includes psychoeducation, VR exposure, cognitive techniques, monitoring of symptoms, and relapse prevention. The primary outcome measure will be the Acrophobia Questionnaire. Secondary outcome measures will include user-friendliness, symptoms of anxiety, depression, and mastery. Assessments will take place online at baseline, directly after the intervention (post test) and at follow-up (3 months). DISCUSSION: This study capitalizes on novel technology and recent scientific advances to develop an affordable and scalable treatment modality. TRIAL REGISTRATION: Netherlands Trial Register: NTR6442. Registered on 29 June 2017. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-018-2704-6) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-09 /pmc/articles/PMC6085658/ /pubmed/30092844 http://dx.doi.org/10.1186/s13063-018-2704-6 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Donker, T.
Van Esveld, S.
Fischer, N.
Van Straten, A.
0Phobia – towards a virtual cure for acrophobia: study protocol for a randomized controlled trial
title 0Phobia – towards a virtual cure for acrophobia: study protocol for a randomized controlled trial
title_full 0Phobia – towards a virtual cure for acrophobia: study protocol for a randomized controlled trial
title_fullStr 0Phobia – towards a virtual cure for acrophobia: study protocol for a randomized controlled trial
title_full_unstemmed 0Phobia – towards a virtual cure for acrophobia: study protocol for a randomized controlled trial
title_short 0Phobia – towards a virtual cure for acrophobia: study protocol for a randomized controlled trial
title_sort 0phobia – towards a virtual cure for acrophobia: study protocol for a randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085658/
https://www.ncbi.nlm.nih.gov/pubmed/30092844
http://dx.doi.org/10.1186/s13063-018-2704-6
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