Antidepressants 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.


Journal

BMC neurology
ISSN: 1471-2377
Titre abrégé: BMC Neurol
Pays: England
ID NLM: 100968555

Informations de publication

Date de publication:
12 Dec 2022
Historique:
received: 28 10 2022
accepted: 25 11 2022
entrez: 12 12 2022
pubmed: 13 12 2022
medline: 15 12 2022
Statut: epublish

Résumé

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. 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. 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. ClinicalTrials.gov Identifier: NCT03652870 Date of registration - 29

Sections du résumé

BACKGROUND BACKGROUND
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.
METHODS METHODS
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.
DISCUSSION CONCLUSIONS
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.
TRIAL REGISTRATION BACKGROUND
ClinicalTrials.gov Identifier: NCT03652870 Date of registration - 29

Identifiants

pubmed: 36510237
doi: 10.1186/s12883-022-02988-5
pii: 10.1186/s12883-022-02988-5
pmc: PMC9743717
doi:

Substances chimiques

Escitalopram 4O4S742ANY
Antidepressive Agents 0
Nortriptyline BL03SY4LXB

Banques de données

ClinicalTrials.gov
['NCT03652870']

Types de publication

Clinical Trial Protocol Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

474

Subventions

Organisme : Health Technology Assessment Programme
ID : 16/145/01
Organisme : Cure Parkinson's Trust
ID : 3013387

Informations de copyright

© 2022. The Author(s).

Références

Lancet Neurol. 2022 Jan;21(1):89-102
pubmed: 34942142
Drug Saf. 1998 Jul;19(1):11-22
pubmed: 9673855
Parkinsonism Relat Disord. 2018 Jul;52:83-89
pubmed: 29625875
J Clin Psychiatry. 1996 Oct;57(10):449-54
pubmed: 8909330
Health Technol Assess. 2005 May;9(16):1-134, iii
pubmed: 15876362
Neurology. 1994 Dec;44(12):2406
pubmed: 7991139
Mov Disord. 2008 Apr 30;23(6):850-7
pubmed: 18311826
Mov Disord. 2000 Sep;15(5):986-9
pubmed: 11009210
Neurology. 2009 Mar 10;72(10):886-92
pubmed: 19092112
Ann Gen Psychiatry. 2010 Jan 18;9:5
pubmed: 20148108
Neurology. 2012 Apr 17;78(16):1229-36
pubmed: 22496199
Psychol Med. 2015 Nov;45(15):3269-79
pubmed: 26165748
Mov Disord. 2008 Jan 30;23(2):183-9; quiz 313
pubmed: 17987654
Int J Geriatr Psychiatry. 2004 Jan;19(1):9-18
pubmed: 14716694
Osteoporos Int. 2016 Nov;27(11):3187-3195
pubmed: 27311722
Neurology. 1993 Jan;43(1):211-3
pubmed: 8423889
Neurobiol Dis. 2017 Oct;106:191-204
pubmed: 28711409
PLoS One. 2013 Oct 02;8(10):e76651
pubmed: 24098546
J Affect Disord. 2000 Apr;58(1):19-36
pubmed: 10760555
Acta Neurol Belg. 2010 Jun;110(2):148-56
pubmed: 20873444
Psychol Med. 2001 Jan;31(1):65-73
pubmed: 11200961
Psychol Med. 1992 May;22(2):465-86
pubmed: 1615114
J Neurol Neurosurg Psychiatry. 2000 Sep;69(3):308-12
pubmed: 10945804
Lancet. 2017 Oct 7;390(10103):1664-1675
pubmed: 28781108

Auteurs

A Schrag (A)

Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, UK. a.schrag@ucl.ac.uk.
Department of Neurology, Royal Free London NHS Foundation Trust, London, UK. a.schrag@ucl.ac.uk.

C Carroll (C)

Faculty of Medicine and Dentistry, University of Plymouth, Plymouth, UK.

G Duncan (G)

NHS Lothian, Edinburgh, UK.

S Molloy (S)

Department of Neurosciences, Imperial College Healthcare NHS Trust, London, UK.

L Grover (L)

Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, UK.

R Hunter (R)

Research Department of Primary Care and Population Health, University College London, London, UK.

R Brown (R)

Department of Psychology, Institute of Psychiatry, King's College London, London, UK.

N Freemantle (N)

Comprehensive Clinical Trials Unit, University College London, London, UK.

J Whipps (J)

PPI Representative, Plymouth, UK.

M A Serfaty (MA)

Division of Psychiatry, UCL, London, UK.
Priory Hospital North London, London, UK.

G Lewis (G)

Division of Psychiatry, UCL, London, UK.

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