Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/36827
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dc.contributor.authorWileman, Varien_UK
dc.contributor.authorMcGuinness, Serenaen_UK
dc.contributor.authorSweeney, Louiseen_UK
dc.contributor.authorNorton, Christineen_UK
dc.contributor.authorMiller, Lauraen_UK
dc.contributor.authorStagg, Imogenen_UK
dc.contributor.authorO’Carroll, Ronanen_UK
dc.contributor.authorMoss-Morris, Ronaen_UK
dc.date.accessioned2025-03-11T01:41:29Z-
dc.date.available2025-03-11T01:41:29Z-
dc.date.issued2024-07-12en_UK
dc.identifier.other476en_UK
dc.identifier.urihttp://hdl.handle.net/1893/36827-
dc.description.abstractBackground Participants in research trials often disclose severe depression symptoms, including thoughts of self-harm and suicidal ideation, in validated self-administered questionnaires such as the Patient Health Questionnaire (PHQ-9). However, there is no standard protocol for responding to such disclosure, and the opportunity to support people at risk is potentially missed. We developed and evaluated a risk assessment protocol for the IBD-BOOST randomised controlled trial (ISRCTN71618461 09/09/2019). Methods Participants completed the PHQ-9 at baseline and 6-month and 12-month follow-ups. The trial database automatically alerted the research team to risk assess participants. Trial researchers, trained in the protocol, contacted participants by telephone, completed the risk assessment, and signposted participants to appropriate professional services. Results Seven hundred eighty participants were randomised in the trial; 41 required risk assessment. One participant declined assessment, so 40 risk assessments were completed. Twenty-four participants were assessed as low-risk and 16 participants as medium-risk, with 12 declaring previous suicide attempts. None were rated as high-risk. Trial participants expressed appreciation for being contacted, and all except two wished to receive information about professional support services. Trial risk assessors reported positive experiences of conducting the risk assessment with suggestions for improvement, which resulted in minor modifications to the protocol. Discussion Our evaluation demonstrated that it was viable for a research trial team to successfully conduct a risk-assessment protocol for trial participants reporting thoughts of self-harm, with training and support from senior colleagues. Resources are required for training and delivery, but it is not unduly onerous. Trial participants appeared to find completing the assessment acceptable.en_UK
dc.language.isoenen_UK
dc.publisherSpringer Science and Business Media LLCen_UK
dc.relationWileman V, McGuinness S, Sweeney L, Norton C, Miller L, Stagg I, O’Carroll R & Moss-Morris R (2024) Development and preliminary evaluation of a suicidal risk assessment protocol in a randomised controlled trial using the Patient Health Questionnaire (PHQ-9). <i>Trials</i>, 25, Art. No.: 476. https://doi.org/10.1186/s13063-024-08276-6en_UK
dc.rightsThis 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.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.subjectPHQ-9en_UK
dc.subjectSelf-harmen_UK
dc.subjectSuicideen_UK
dc.subjectIdeationen_UK
dc.subjectDepressionen_UK
dc.subjectTrialsen_UK
dc.subjectRisk-assessmenten_UK
dc.subjectLong-term conditionsen_UK
dc.subjectProtocolen_UK
dc.titleDevelopment and preliminary evaluation of a suicidal risk assessment protocol in a randomised controlled trial using the Patient Health Questionnaire (PHQ-9)en_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1186/s13063-024-08276-6en_UK
dc.identifier.pmid38997767en_UK
dc.citation.jtitleTrialsen_UK
dc.citation.issn1745-6215en_UK
dc.citation.volume25en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.contributor.funderNational Institutes of Healthen_UK
dc.author.emailronan.ocarroll@stir.ac.uken_UK
dc.citation.date12/07/2024en_UK
dc.contributor.affiliationKing's College Londonen_UK
dc.contributor.affiliationKing's College Londonen_UK
dc.contributor.affiliationKing's College Londonen_UK
dc.contributor.affiliationKing's College Londonen_UK
dc.contributor.affiliationQueen Mary, University of Londonen_UK
dc.contributor.affiliationSt Mark's Hospital and Academic Instituteen_UK
dc.contributor.affiliationPsychologyen_UK
dc.contributor.affiliationKing's College Londonen_UK
dc.identifier.isiWOS:001271442200002en_UK
dc.identifier.scopusid2-s2.0-85198492936en_UK
dc.identifier.wtid2075901en_UK
dc.contributor.orcid0000-0002-9673-8047en_UK
dc.contributor.orcid0000-0002-5130-291Xen_UK
dc.date.accepted2024-06-18en_UK
dcterms.dateAccepted2024-06-18en_UK
dc.date.filedepositdate2025-01-28en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorWileman, Vari|0000-0002-9673-8047en_UK
local.rioxx.authorMcGuinness, Serena|en_UK
local.rioxx.authorSweeney, Louise|en_UK
local.rioxx.authorNorton, Christine|en_UK
local.rioxx.authorMiller, Laura|en_UK
local.rioxx.authorStagg, Imogen|en_UK
local.rioxx.authorO’Carroll, Ronan|0000-0002-5130-291Xen_UK
local.rioxx.authorMoss-Morris, Rona|en_UK
local.rioxx.projectProject ID unknown|National Institutes of Health|http://dx.doi.org/10.13039/100000002en_UK
local.rioxx.freetoreaddate2025-01-28en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2025-01-28|en_UK
local.rioxx.filenames13063-024-08276-6.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source1745-6215en_UK
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