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dc.contributor.authorvan Loggerenberg, F
dc.contributor.authorMcGrath, M
dc.contributor.authorAkena, D
dc.contributor.authorBirabwa-Oketcho, H
dc.contributor.authorMéndez, CAC
dc.contributor.authorGómez-Restrepo, C
dc.contributor.authorDžubur Kulenoviĉ, A
dc.contributor.authorMuhić, M
dc.contributor.authorSewankambo, NK
dc.contributor.authorSikira, H
dc.contributor.authorPriebe, S
dc.date.accessioned2021-10-28T14:54:51Z
dc.date.available2021-09-07
dc.date.available2021-10-28T14:54:51Z
dc.date.issued2021-09-30
dc.identifier.issn2055-5784
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/74830
dc.description.abstractBACKGROUND: DIALOG+ is a resource-oriented and evidence-based intervention to improve quality of life and reduce mental distress. While it has been extensively studied in mental health care, there is little evidence for how to use it in primary care settings for patients with chronic physical conditions. Considering that DIALOG+ is used in existing routine patient-clinician meetings and is very low cost, it may have the potential to help large numbers of patients with chronic physical conditions, mental distress and poor quality of life who are treated in primary care. This is particularly relevant in low- and middle-income countries (LMICs) where resources for specialised services for such patients are scarce or non-existent. METHODS: An exploratory non-controlled trial will be conducted to primarily assess the feasibility and acceptability and, secondarily, outcomes of delivering DIALOG+ to patients with chronic physical conditions and poor quality of life in primary care settings in Bosnia and Herzegovina, Colombia and Uganda. Thirty patients in each country will receive DIALOG+ up to three times in monthly meetings over a 3-month period. Feasibility will be assessed by determining the extent to which the intervention is implemented as planned. Experiences will be captured in interviews and focus groups with care providers and participants to understand acceptability. Quality of life, symptoms of anxiety and depression, objective social situation and health status will be assessed at baseline and again after the three-session intervention. DISCUSSION: This study will inform our understanding of the extent to which DIALOG+ may be used in the routine care of patients with chronic physical conditions in different primary care settings. The findings of this exploratory trial can inform the design of future full randomised controlled trials of DIALOG+ in primary care settings in LMICs. TRIAL REGISTRATION: All studies were registered prospectively (on 02/12/2020 for Uganda and Bosnia and Herzegovina, and 01/12/2020 for Colombia) within the ISRCTN Registry. ISRCTN17003451 (Bosnia and Herzegovina), ISRCTN14018729 (Colombia) and ISRCTN50335796 (Uganda). Protocol version and date: v2.0; 28/07/2020 (Bosnia and Herzegovina), v0.3 02/08/2020 (Colombia) and v1.0, 05/11/2020 (Uganda).en_US
dc.format.extent180 - ?
dc.languageeng
dc.relation.ispartofPilot Feasibility Stud
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subjectDIALOG+en_US
dc.subjectGlobal mental healthen_US
dc.subjectLMICsen_US
dc.subjectPrimary careen_US
dc.subjectPsychosocial interventionsen_US
dc.subjectQuality of lifeen_US
dc.subjectResource-oriented approachen_US
dc.subjectSolution-focuseden_US
dc.titleFeasibility, experiences and outcomes of using DIALOG+ in primary care to improve quality of life and mental distress of patients with chronic conditions: an exploratory non-controlled trial in Bosnia and Herzegovina, Colombia and Uganda.en_US
dc.typeArticleen_US
dc.identifier.doi10.1186/s40814-021-00914-z
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/34593055en_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
pubs.volume7en_US
dcterms.dateAccepted2021-09-07
qmul.funderNIHR Global Health Research Group on developing psycho-social interventions for mental health care::National Institute for Health Researchen_US


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Attribution 3.0 United States
Except where otherwise noted, this item's license is described as Attribution 3.0 United States