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The PTSD help app in a Danish PTSD population: research protocol of a randomized controlled feasibility trial

BACKGROUND: Due to an increase in PTSD patients seeking help in the Danish mental health sector and the addition of Complex PTSD to the ICD-11, there is a need to increase efficiency of existing treatments for PTSD. mHealth interventions have been shown to reduce PTSD symptoms. Therefore, the implem...

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Autores principales: Scharff, Frederik Bernt, Lau, Marianne Engelbrecht, Riisager, Lisa Helena Grønberg, Møller, Stine Bjerrum, Salimi, Mehrak Lykkeberg, Gondan, Matthias, Folke, Sofie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7325563/
https://www.ncbi.nlm.nih.gov/pubmed/32617173
http://dx.doi.org/10.1186/s40814-020-00633-x
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author Scharff, Frederik Bernt
Lau, Marianne Engelbrecht
Riisager, Lisa Helena Grønberg
Møller, Stine Bjerrum
Salimi, Mehrak Lykkeberg
Gondan, Matthias
Folke, Sofie
author_facet Scharff, Frederik Bernt
Lau, Marianne Engelbrecht
Riisager, Lisa Helena Grønberg
Møller, Stine Bjerrum
Salimi, Mehrak Lykkeberg
Gondan, Matthias
Folke, Sofie
author_sort Scharff, Frederik Bernt
collection PubMed
description BACKGROUND: Due to an increase in PTSD patients seeking help in the Danish mental health sector and the addition of Complex PTSD to the ICD-11, there is a need to increase efficiency of existing treatments for PTSD. mHealth interventions have been shown to reduce PTSD symptoms. Therefore, the implementation of a mHealth intervention designed for psychiatric PTSD patients as a therapy add-on may improve treatment outcome. No study to date has explored the effects of mHealth interventions for PTSD in the Danish mental health sector, the feasibility and effect of this type of intervention needs testing. METHODS: The study is an investigator-initiated randomized controlled feasibility trial investigating the clinical mHealth tool PTSD help combined with care as usual (CAU) compared to CAU for adults with PTSD. Seventy patients will be recruited and receive either the mHealth intervention combined with CAU or CAU alone. The primary feasibility outcome is the proportion of eligible patients that participate in the study until the end assessment. Secondary outcome data consists of the fraction of compliant patients in the experimental group and exploratory data on PTSD help on PTSD symptom severity, level of psychological distress, sleep quality, dissociation symptoms, therapy readiness, quality of life, disability levels, and recovery. DISCUSSION: This study may help increase our knowledge of possible benefits of, as well as potential barriers to, the implementation of mHealth tools in the psychiatric sector. It may also provide a cost-efficient means to increase therapy outcomes and decrease the duration of suffering for PTSD patients in the psychiatric sector. TRIAL REGISTRATION: The trial is registered at ClinicalTrials.gov (ID: NCT03862703) https://clinicaltrials.gov/ct2/show/NCT03862703 on the 27 of February 2019 and has been approved by the Danish Data Protection Agency (journal number: VD-2018-200 ISuite number 6443). Referring to the committee law §2, the National Committee on Health Research Ethics (DNVK) [H-18024180] decided that the study could proceed without approval as the use of PTSD help did not constitute a health science intervention according to Danish health science legislation.
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spelling pubmed-73255632020-07-01 The PTSD help app in a Danish PTSD population: research protocol of a randomized controlled feasibility trial Scharff, Frederik Bernt Lau, Marianne Engelbrecht Riisager, Lisa Helena Grønberg Møller, Stine Bjerrum Salimi, Mehrak Lykkeberg Gondan, Matthias Folke, Sofie Pilot Feasibility Stud Study Protocol BACKGROUND: Due to an increase in PTSD patients seeking help in the Danish mental health sector and the addition of Complex PTSD to the ICD-11, there is a need to increase efficiency of existing treatments for PTSD. mHealth interventions have been shown to reduce PTSD symptoms. Therefore, the implementation of a mHealth intervention designed for psychiatric PTSD patients as a therapy add-on may improve treatment outcome. No study to date has explored the effects of mHealth interventions for PTSD in the Danish mental health sector, the feasibility and effect of this type of intervention needs testing. METHODS: The study is an investigator-initiated randomized controlled feasibility trial investigating the clinical mHealth tool PTSD help combined with care as usual (CAU) compared to CAU for adults with PTSD. Seventy patients will be recruited and receive either the mHealth intervention combined with CAU or CAU alone. The primary feasibility outcome is the proportion of eligible patients that participate in the study until the end assessment. Secondary outcome data consists of the fraction of compliant patients in the experimental group and exploratory data on PTSD help on PTSD symptom severity, level of psychological distress, sleep quality, dissociation symptoms, therapy readiness, quality of life, disability levels, and recovery. DISCUSSION: This study may help increase our knowledge of possible benefits of, as well as potential barriers to, the implementation of mHealth tools in the psychiatric sector. It may also provide a cost-efficient means to increase therapy outcomes and decrease the duration of suffering for PTSD patients in the psychiatric sector. TRIAL REGISTRATION: The trial is registered at ClinicalTrials.gov (ID: NCT03862703) https://clinicaltrials.gov/ct2/show/NCT03862703 on the 27 of February 2019 and has been approved by the Danish Data Protection Agency (journal number: VD-2018-200 ISuite number 6443). Referring to the committee law §2, the National Committee on Health Research Ethics (DNVK) [H-18024180] decided that the study could proceed without approval as the use of PTSD help did not constitute a health science intervention according to Danish health science legislation. BioMed Central 2020-06-30 /pmc/articles/PMC7325563/ /pubmed/32617173 http://dx.doi.org/10.1186/s40814-020-00633-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Study Protocol
Scharff, Frederik Bernt
Lau, Marianne Engelbrecht
Riisager, Lisa Helena Grønberg
Møller, Stine Bjerrum
Salimi, Mehrak Lykkeberg
Gondan, Matthias
Folke, Sofie
The PTSD help app in a Danish PTSD population: research protocol of a randomized controlled feasibility trial
title The PTSD help app in a Danish PTSD population: research protocol of a randomized controlled feasibility trial
title_full The PTSD help app in a Danish PTSD population: research protocol of a randomized controlled feasibility trial
title_fullStr The PTSD help app in a Danish PTSD population: research protocol of a randomized controlled feasibility trial
title_full_unstemmed The PTSD help app in a Danish PTSD population: research protocol of a randomized controlled feasibility trial
title_short The PTSD help app in a Danish PTSD population: research protocol of a randomized controlled feasibility trial
title_sort ptsd help app in a danish ptsd population: research protocol of a randomized controlled feasibility trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7325563/
https://www.ncbi.nlm.nih.gov/pubmed/32617173
http://dx.doi.org/10.1186/s40814-020-00633-x
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