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dc.contributor.authorSchrag, A
dc.contributor.authorCarroll, Camille
dc.contributor.authorDuncan, G
dc.contributor.authorMolloy, S
dc.contributor.authorGrover, L
dc.contributor.authorHunter, R
dc.contributor.authorBrown, R
dc.contributor.authorFreemantle, N
dc.contributor.authorWhipps, J
dc.contributor.authorSerfaty, MA
dc.contributor.authorLewis, G
dc.date.accessioned2023-01-16T14:47:25Z
dc.date.issued2022-12-12
dc.identifier.issn1471-2377
dc.identifier.issn1471-2377
dc.identifier.other474
dc.identifier.urihttp://hdl.handle.net/10026.1/20174
dc.description.abstract

<jats:title>Abstract</jats:title><jats:sec> <jats:title>Background</jats:title> <jats:p>Depressive symptoms are common in patients with Parkinson’s disease and depression is a significant predictor of functional impairment, reduced quality of life and general well-being in Parkinson's disease. Despite the high prevalence of depression, evidence on the effectiveness and tolerability of antidepressants in this population is limited. The primary aim of this trial is to establish the clinical and cost effectiveness of escitalopram and nortriptyline for the treatment of depression in Parkinson’s disease.</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>This is a multi-centre, double-blind, randomised placebo-controlled trial in 408 people with Parkinson’s disease with subsyndromal depression, major depressive disorder or persistent depressive disorder and a Beck Depression Inventory-II (BDI-II) score of 14 or above. Participants will be randomised into one of three groups, receiving either escitalopram, nortriptyline or placebo for 12 months. Trial participation is face-to-face, hybrid or remote. The primary outcome measure is the BDI-II score following 8 weeks of treatment. Secondary outcomes will be collected at baseline, 8, 26 and 52 weeks and following withdrawal, including severity of anxiety and depression scores as well as Parkinson’s disease motor severity, and ratings of non-motor symptoms, cognitive function, health-related quality of life, levodopa-equivalence dose, changes in medication, overall clinical effectiveness, capability, health and social care resource use, carer health-related quality of life, adverse effects and number of dropouts.</jats:p> </jats:sec><jats:sec> <jats:title>Discussion</jats:title> <jats:p>This trial aims to determine the effectiveness of escitalopram and nortriptyline for reducing depressive symptoms in Parkinson’s disease over 8 weeks, to provide information on the effect of these medications on anxiety and other non-motor symptoms in PD and on impact on patients and caregivers, and to examine their effect on change in motor severity.</jats:p> </jats:sec><jats:sec> <jats:title>Trial registration</jats:title> <jats:p>ClinicalTrials.gov Identifier: NCT03652870</jats:p> <jats:p>Date of registration – 29<jats:sup>th</jats:sup> August 2018</jats:p> </jats:sec>

dc.format.extent474-
dc.format.mediumElectronic
dc.languageen
dc.language.isoeng
dc.publisherSpringer Science and Business Media LLC
dc.subjectParkinson's disease
dc.subjectDepressive symptoms
dc.subjectEscitalopram
dc.subjectNortriptyline
dc.subjectRandomised controlled trial
dc.subjectClinical effectiveness
dc.subjectCost-effectiveness
dc.titleAntidepressants Trial in Parkinson's Disease (ADepT-PD): protocol for a randomised placebo-controlled trial on the effectiveness of escitalopram and nortriptyline on depressive symptoms in Parkinson’s disease
dc.typejournal-article
dc.typeClinical Trial Protocol
dc.typeJournal Article
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000898457900003&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue1
plymouth.volume22
plymouth.publication-statusPublished online
plymouth.journalBMC Neurology
dc.identifier.doi10.1186/s12883-022-02988-5
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/Peninsula Medical School
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA03 Allied Health Professions, Dentistry, Nursing and Pharmacy
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/FoH - Applied Parkinson's Research
plymouth.organisational-group/Plymouth/Research Groups/FoH - Community and Primary Care
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)/CCT&PS
plymouth.organisational-group/Plymouth/Research Groups/Plymouth Institute of Health and Care Research (PIHR)
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeEngland
dcterms.dateAccepted2022-11-25
dc.rights.embargodate2023-1-17
dc.identifier.eissn1471-2377
rioxxterms.versionofrecord10.1186/s12883-022-02988-5
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2022-12-12
rioxxterms.typeJournal Article/Review


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