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dc.contributor.authorKendrick, Ten_US
dc.contributor.authorDowrick, Cen_US
dc.contributor.authorLewis, Gen_US
dc.contributor.authorMoore, Men_US
dc.contributor.authorLeydon, Gen_US
dc.contributor.authorGeraghty, AWAen_US
dc.contributor.authorGriffiths, Gen_US
dc.contributor.authorZhu, Sen_US
dc.contributor.authorYao, Gen_US
dc.contributor.authorMay, Cen_US
dc.contributor.authorGabbay, Men_US
dc.contributor.authorDewar-Haggart, Ren_US
dc.contributor.authorWilliams, Sen_US
dc.contributor.authorBui, Len_US
dc.contributor.authorThompson, Nen_US
dc.contributor.authorBridewell, Len_US
dc.contributor.authorTrapasso, Een_US
dc.contributor.authorPatel, Ten_US
dc.contributor.authorMcCarthy, Men_US
dc.contributor.authorKhan, Nen_US
dc.contributor.authorPage, Hen_US
dc.contributor.authorCorcoran, Een_US
dc.contributor.authorHahn, JSen_US
dc.contributor.authorBird, Men_US
dc.contributor.authorLogan, MXen_US
dc.contributor.authorChing, BCFen_US
dc.contributor.authorTiwari, Ren_US
dc.contributor.authorHunt, Aen_US
dc.contributor.authorStuart, Ben_US
dc.date.accessioned2024-03-06T12:04:55Z
dc.date.available2024-02-19en_US
dc.date.issued2024-02-26en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/95104
dc.description.abstractBACKGROUND: Outcome monitoring of depression is recommended but lacks evidence of patient benefit in primary care. AIM: To test monitoring depression using the PHQ-9 questionnaire with patient feedback. DESIGN AND SETTING: Open cluster-randomised controlled trial in 141 group practices. METHOD: Adults with new depressive episodes were recruited through records searches and opportunistically. EXCLUSION CRITERIA: dementia, psychosis, substance misuse, suicide risk. The PHQ-9 questionnaire was to be administered soon after diagnosis, and 10-35 days later. PRIMARY OUTCOME: Beck Depression Inventory (BDI-II) score at 12 weeks. SECONDARY OUTCOMES: BDI-II at 26 weeks; Work and Social Adjustment Scale and EuroQol EQ-5D-5L quality of life at 12 and 26 weeks; antidepressant treatment, mental health service use, adverse events, and Medical Informant Satisfaction Scale over 26 weeks. RESULTS: 302 intervention arm patients were recruited and 227 controls. At 12 weeks 252 (83.4%) and 195 (85.9%) were followed-up respectively. Only 41% of intervention arm patients had a GP follow-up PHQ-9 recorded. There was no significant difference in BDI-II score at 12 weeks (mean difference -0.46; 95% CI -2.16,1.26), adjusted for baseline depression, baseline anxiety, sociodemographic factors, and clustering by practice). EQ-5D-5L quality of life scores were higher in the intervention arm at 26 weeks (adjusted mean difference 0.053; 95% CI 0.093,0.013). A clinically significant difference in depression at 26 weeks could not be ruled out. No significant differences were found in social functioning, adverse events, or satisfaction. In a per-protocol analysis, antidepressant use and mental health contacts were significantly greater in intervention arm patients with a recorded follow-up PHQ-9. CONCLUSIONS: No evidence was found of improved depression outcome at 12 weeks from monitoring. The findings of possible benefits over 26 weeks warrant replication, investigating possible mechanisms, preferably with automated delivery of monitoring and more instructive feedback.en_US
dc.languageengen_US
dc.relation.ispartofBr J Gen Practen_US
dc.rightsThis article is Open Access: CC BY license (https://creativecommons.org/licenses/by/4.0/)
dc.subjectDepressionen_US
dc.subjectMental Healthen_US
dc.subjectMood Disordersen_US
dc.subjectPatient Reported Outcome Measuresen_US
dc.subjectPrimary Health Careen_US
dc.titleDepression follow-up monitoring with the PHQ-9: open cluster-randomised controlled trial.en_US
dc.typeArticle
dc.rights.holder© 2024, The Authors
dc.identifier.doi10.3399/BJGP.2023.0539en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/38408790en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
dcterms.dateAccepted2024-02-19en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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