Evidence map›Paper›PMID 32404379›Full record

ReviewJournal of neurology, neurosurgery, and psychiatry2020

Clinical trials in REM sleep behavioural disorder: challenges and opportunities.

Aleksandar Videnovic, Yo-El S Ju, Isabelle Arnulf, Valérie Cochen-De Cock, Birgit Högl, Dieter Kunz, Federica Provini, Pietro-Luca Ratti, Mya C Schiess, Carlos H Schenck and 2 more

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of neurology, neurosurgery, and psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
5.7field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 2 syntheses or guidelines pooled it, 93 citations in OpenAlex.

  1. Guideline
  2. Sleep disturbances in Lewy body dementia: A systematic review.International journal of geriatric psychiatry · 2022
    Pooled it
  3. Baseline characteristics of the North American prodromal Synucleinopathy cohort.Annals of clinical and translational neurology · 2023
    Trial
  4. Observational
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 9 institutions in 6 countries.

Aleksandar VidenovicDepartment of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA AVIDENOVIC@mgh.harvard.edu.ORCID 0000-0002-9237-1516
Yo-El S JuDepartment of Neurology, Washington University in Saint Louis, Saint Louis, Missouri, USA.
Isabelle ArnulfAssistance Publique Hôpitaux de Paris, Service des pathologies du Sommeil, Hôpital Pitié-Salpêtrière, Paris, France.
Valérie Cochen-De CockNeurologie et sommeil, Clinique Beau Soleil, Montpellier, France.ORCID 0000-0002-6460-4319
Birgit HöglDepartment of Neurology, Innsbruck Medical University, Innsbruck, Austria.
Dieter KunzClinic for Sleep and Chronomedicine, Berlin, Germany.
Federica ProviniIRCCS Institute of Neurological Sciences of Bologna, University of Bologna, Bologna, Italy.
Pietro-Luca RattiNeurocenter of Southern Switzerland, Lugano, Switzerland.
Mya C SchiessDepartment of Neurology, University of Texas Medical School at Houston, Houston, Texas, USA.
Carlos H SchenckDepartment of Psychiatry, University of Minnesota, Minneapolis, Minnesota, USA.
Claudia TrenkwalderParacelsus Elena Klinik, Kassel, Germany.
Treatment and Trials Working Group of the International RBD Study Group
Centre National de la Recherche Scientifique · FRInnsbruck Medical University · ATInstitute of Neurological Sciences · ITLaboratory for Biomedical Neurosciences · CHMassachusetts General Hospital · USUniversitätsmedizin Göttingen · DEUniversité de Montpellier · FRUniversity of Minnesota · USWashington University in St. Louis · US

Funding

WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Washington University Institute of Clinical and Translational Sciences (UL1)UL1RR024992 · NCRR · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2007 to 2011
$45.4M
Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
Washington University Institute of Clinical and Translational Sciences (KL2) KL2TR002346 · NCATS · WASHINGTON UNIVERSITY · PI Dominic N Reeds · 2017 to 2026
$14.0M
Washington University Institute of Clinical and Translational SciencesKL2TR000450 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$8.8M
Bright light modulation of non-motor symptoms in Parkinson's diseaseR01NS099055 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI VIDENOVIC, ALEKSANDAR · 2017 to 2021
$3.0M
Neuroprotective Treatment Trial Planning in REM Sleep Behavior DisorderR34AG056639 · NIA · WASHINGTON UNIVERSITY · PI BOEVE, BRADLEY F, JU, YO-EL S · 2018 to 2019
$1.2M
TARGETING SLOW WAVE SLEEP TO CONTROL NEURONAL ACTIVITY AND AMYLOID-BETA DYNAMICSK23NS089922 · NINDS · WASHINGTON UNIVERSITY · PI JU, YO-EL S · 2015 to 2019
$889k
Circadian Rhythms Regulation in Pre-Manifest SynucleinopathiesR21NS108022 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI VIDENOVIC, ALEKSANDAR · 2018 to 2019
$463k
NCATS NIH HHS KL2 TR000450NCATS NIH HHS KL2 TR002346NCATS NIH HHS UL1 TR000448NCATS NIH HHS UL1 TR002345NCRR NIH HHS UL1 RR024992NIA NIH HHS R34 AG056639NINDS NIH HHS K23 NS089922NINDS NIH HHS R01 NS099055NINDS NIH HHS R21 NS108022
6 · The paper itself

Abstract

The rapid eye movement sleep behavioural disorder (RBD) population is an ideal study population for testing disease-modifying treatments for synucleinopathies, since RBD represents an early prodromal stage of synucleinopathy when neuropathology may be more responsive to treatment. While clonazepam and melatonin are most commonly used as symptomatic treatments for RBD, clinical trials of symptomatic treatments are also needed to identify evidence-based treatments. A comprehensive framework for both disease-modifying and symptomatic treatment trials in RBD is described, including potential treatments in the pipeline, cost-effective participant recruitment and selection, study design, outcomes and dissemination of results. For disease-modifying treatment clinical trials, the recommended primary outcome is phenoconversion to an overt synucleinopathy, and stratification features should be used to select a study population at high risk of phenoconversion, to enable more rapid clinical trials. For symptomatic treatment clinical trials, objective polysomnogram-based measurement of RBD-related movements and vocalisations should be the primary outcome measure, rather than subjective scales or diaries. Mobile technology to enable objective measurement of RBD episodes in the ambulatory setting, and advances in imaging, biofluid, tissue, and neurophysiological biomarkers of synucleinopathies, will enable more efficient clinical trials but are still in development. Increasing awareness of RBD among the general public and medical community coupled with timely diagnosis of these diseases will facilitate progress in the development of therapeutics for RBD and associated neurodegenerative disorders.

Indexed as

Clinical Trials as TopicHumansREM Sleep Behavior DisorderResearch DesignSleep, REMLewy body dementiaParkinson's diseaserandomised trialssleep disorders

Identifiers

PMID32404379
PMCPMC7735522
OpenAlexW3025392679

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.