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  4. A smartphone application for treating depressive symptoms: study protocol for a randomised controlled trial
 
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A smartphone application for treating depressive symptoms: study protocol for a randomised controlled trial
File(s)
Deady_A smartphone application for treating_BMC.pdf (793.6 KB)
Published version
OA Location
https://bmcpsychiatry.biomedcentral.com/articles/10.1186/s12888-018-1752-5
Author(s)
Deady, M
Johnston, DA
Glozier, N
Milne, D
Choi, I
more
Type
Journal Article
Abstract
BACKGROUND: Depression is a commonly occurring disorder linked to diminished role functioning and quality of life. The development of treatments that overcome barriers to accessing treatment remains an important area of clinical research as most people delay or do not receive treatment at an appropriate time. The workplace is an ideal setting to roll-out an intervention, particularly given the substantial psychological benefits associated with remaining in the workforce. Mobile health (mhealth) interventions utilising smartphone applications (apps) offer novel solutions to disseminating evidence based programs, however few apps have undergone rigorous testing. The present study aims to evaluate the effectiveness of a smartphone app designed to treat depressive symptoms in workers. METHODS: The present study is a multicentre randomised controlled trial (RCT), comparing the effectiveness of the intervention to that of an attention control. The primary outcome measured will be reduced depressive symptoms at 3 months. Secondary outcomes such as wellbeing and work performance will also be measured. Employees from a range of industries will be recruited via a mixture of targeted social media advertising and Industry partners. Participants will be included if they present with likely current depression at baseline. Following baseline assessment (administered within the app), participants will be randomised to receive one of two versions of the Headgear application: 1) Intervention (a 30-day mental health intervention focusing on behavioural activation and mindfulness), or 2) attention control app (mood monitoring for 30 days). Participants will be blinded to their allocation. Analyses will be conducted within an intention to treat framework using mixed modelling. DISCUSSION: The results of this trial will provide valuable information about the effectiveness of mhealth interventions in the treatment of depressive symptoms in a workplace context. TRIAL REGISTRATION: The current trial is registered with the Australian and New Zealand Clinical Trials Registry ( ACTRN12617000547347 , Registration date: 19/04/2017).
Date Issued
2018-06-01
Date Acceptance
2018-05-17
Citation
BMC Psychiatry, 2018, 18 (1), pp.166-166
URI
http://hdl.handle.net/10044/1/71054
DOI
https://www.dx.doi.org/10.1186/s12888-018-1752-5
ISSN
1471-244X
Publisher
BioMed Central
Start Page
166
End Page
166
Journal / Book Title
BMC Psychiatry
Volume
18
Issue
1
Copyright Statement
© The Author(s). 2018. This article is distributed under the terms of the Creative Commons Attribution 4.0International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, andreproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link tothe 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.
Identifier
https://www.ncbi.nlm.nih.gov/pubmed/29859060
PII: 10.1186/s12888-018-1752-5
Subjects
Depression
Mhealth
Treatment
Workplace
Adult
Clinical Protocols
Cognitive Behavioral Therapy
Depression
Depressive Disorder
Female
Humans
Male
Mobile Applications
Randomized Controlled Trials as Topic
Research Design
Smartphone
Telemedicine
Therapy, Computer-Assisted
Treatment Outcome
Publication Status
Published
Coverage Spatial
England
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