Albert Leentjens

Prof. Albert Leentjens

orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2019 in Parkinsonism & Related Disorders
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Journal Article
Closed access
AWAmée F. Wolters
Amée F. Wolters
SWSjors C.F. van de Weijer
Sjors C.F. van de Weijer
ALAlbert Leentjens
Albert Leentjens
ADAnnelien Duits
Annelien Duits
Heidi I.L. JacobsHeidi I.L. Jacobs
Heidi I.L. Jacobs
MKMark L. Kuijf
Mark L. Kuijf

17 September 2018 in Movement Disorders
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Journal Article
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RVRachel M. J. van der Velden
Rachel M. J. van der Velden
MBMartijn P. G. Broen
Martijn P. G. Broen
MKMark L. Kuijf
Mark L. Kuijf
ALAlbert Leentjens
Albert Leentjens

1 December 2012 in Parkinsonism & Related Disorders
Verified
Journal Article
Closed access
ALAlbert Leentjens
Albert Leentjens
KDK. Dujardin
K. Dujardin
LML. Marsh
L. Marsh
PMP. Martinez-Martin
P. Martinez-Martin
IRI.H. Richard
I.H. Richard
SSS.E. Starkstein
S.E. Starkstein

22 February 2021 in Movement Disorders
Verified
Journal Article
Open access
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AMAnja J.H. Moonen
Anja J.H. Moonen
AMAnne E.P. Mulders
Anne E.P. Mulders
LDLuc Defebvre
Luc Defebvre
ADAnnelien Duits
Annelien Duits
BFBérengère Flinois
Bérengère Flinois
ALAlbert Leentjens
Albert Leentjens
Background: Anxiety disorders are among the most prevalent and disabling neuropsychiatric syndromes in patients with Parkinsonʼs disease (PD), but no randomized controlled treatment trials of anxiety have been published to date.Objective: The aim of this study was to assess the effectiveness of cognitive behavioral therapy (CBT) in the treatment of anxiety in patients with PD.Methods: Forty‐eight patients with PD with anxiety were randomized 1:1 between CBT and clinical monitoring only (CMO). The CBT program was developed to specifically address anxiety symptoms in PD and consisted of 10 weekly sessions. Assessments were conducted by blinded assessors at baseline, at the end of the intervention, after 3 months, and after 6 months (CBT group only). Main outcome measures were the Hamilton Anxiety Rating Scale (HARS) and the Parkinson Anxiety Scale (PAS).Results: Both the CBT and CMO groups showed clinically relevant improvement. Although there was no between‐group difference in outcome on the Hamilton Anxiety Rating Scale (6.7‐point reduction in the CBT group versus 3.9‐point reduction in the CMO group; P = 0.15), there was both a statistically significant and a clinically relevant between‐group difference on the total PAS in favor of CBT (9.9‐point reduction in the CBT group versus 5.2‐point reduction in the CMO group; P = 0.012), which was due to improvement on the PAS subscales for episodic (situational) anxiety and avoidance behavior. This greater improvement was maintained at 3‐ and 6‐month follow‐ups.Conclusion: CBT is an effective treatment for anxiety in patients with PD and reduces situational and social anxiety, as well as avoidance behavior. © 2021 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society

1 October 2013 in Journal of Psychosomatic Research
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Journal Article
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ALAlbert Leentjens
Albert Leentjens
JLJames L. Levenson
James L. Levenson

4 October 2021 in European Child & Adolescent Psychiatry
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Journal Article
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Natalia SzejkoNatalia Szejko
Natalia Szejko
YWYulia Worbe
Yulia Worbe
AHAndreas Hartmann
Andreas Hartmann
VVVeerle Visser-Vandewalle
Veerle Visser-Vandewalle
LALinda Ackermans
Linda Ackermans
Kirsten Müller-VahlKirsten Müller-Vahl
Kirsten Müller-Vahl
In 2011 the European Society for the Study of Tourette Syndrome (ESSTS) published its first European clinical guidelines for the treatment of Tourette Syndrome (TS) with part IV on deep brain stimulation (DBS). Here, we present a revised version of these guidelines with updated recommendations based on the current literature covering the last decade as well as a survey among ESSTS experts. Currently, data from the International Tourette DBS Registry and Database, two meta-analyses, and eight randomized controlled trials (RCTs) are available. Interpretation of outcomes is limited by small sample sizes and short follow-up periods. Compared to open uncontrolled case studies, RCTs report less favorable outcomes with conflicting results. This could be related to several different aspects including methodological issues, but also substantial placebo effects. These guidelines, therefore, not only present currently available data from open and controlled studies, but also include expert knowledge. Although the overall database has increased in size since 2011, definite conclusions regarding the efficacy and tolerability of DBS in TS are still open to debate. Therefore, we continue to consider DBS for TS as an experimental treatment that should be used only in carefully selected, severely affected and otherwise treatment-resistant patients.