← Back to searchRecruitingRecruiting
North American Prodromal Synucleinopathy Consortium Stage 2
NCT05826457 · Washington University School of Medicine
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
About this study
REM sleep behavior disorder (RBD) is a disorder where people act out their dreams. People with RBD often, but not always, develop Parkinson's Disease, dementia with Lewy bodies, multiple system atrophy, or other neurodegenerative diseases of the synucleinopathy type.
The North American Prodromal Synucleinopathy Consortium Stage 2 (NAPS2) was formed with the purpose of enrolling participants with RBD, in anticipation of a future clinical trial of a neuroprotective trreatment against synucleinopathies. The NAPS Consortium will collect standardized clinical assessments, biofluids, and neuroimaging data. The RBD group will also undergo two overnight sleep studies. Some of this data will be used to develop biomarkers for synucleinopathies in the prodromal (presymptomatic) stage as well as a trial-ready registry of participants.
RBD group procedures include a clinical assessment, questionnaires, blood draw, neuroimaging (MRI and DaTscan), polysomnogram (sleep study), and optional lumbar puncture.
Control group procedures include a clinical assessment, questionnaires, blood draw, neuroimaging (MRI), and lumbar puncture.
Eligibility criteria
Inclusion Criteria for RBD Group
1. Polysomnogram-confirmed RBD by ICSD-3 criteria
2. Capable of providing informed consent at time of study enrollment
3. Age \> 18 years
Exclusion Criteria for RBD Group
1. Diagnosis of PD, dementia of any type, or MSA unless previous participant in NAPS1.
2. Narcolepsy-associated RBD
3. RBD secondary to any known cause except prodromal synucleinopathy.
4. Participation in a clinical trial, except by specific permission by the Executive Committee
5. In the opinion of the investigator, the individual has a clinically significant uncontrolled medical condition that would impede safe completion of the study protocol
Inclusion Criteria for Control Group
1. Ability to provide written consent
2. Age \> 18 years
3. Must meet age, sex, and race matching criteria per the Data Management and Statistical core recommendations for the site
4. Must be willing to undergo all testing procedures, including neuroimaging and lumbar puncture.
5. Normal capacity to perform complex activities of daily living independently based on informant or physician report
Exclusion Criteria for Control Group
1. History of dream enactment behavior to suggest RBD
2. Parkinsonism, MSA, dementia, or mild cognitive impairment
3. Active central nervous system, systemic, psychiatric condition or use of psychoactive medication that would adversely affect cognitive, neuropsychiatric, motor, or autonomic functioning.
4. Contraindications to complete MRI.
5. Contraindications to lumbar puncture.
6. Participation in a clinical trial, except by specific permission by the Executive Committee
7. In the opinion of the investigator, the individual has a clinically significant uncontrolled medical condition that would impede safe completion of the study protocol
Study design
Enrollment target: 500 participants
Age groups: adult, older_adult
Timeline
Starts: 2022-08-12
Estimated completion: 2025-05-01
Last updated: 2024-11-06
Primary outcomes
- • Prodromal Synucleinopathy Rating Scale (up to 5 years)
Sponsor
Washington University School of Medicine · other
With: Mayo Clinic, University of Minnesota, University of California, Los Angeles, McGill University, Emory University, Massachusetts General Hospital, National Institute of Neurological Disorders and Stroke (NINDS), Stanford University, National Institutes of Health (NIH), Oregon Health and Science University, National Institute on Aging (NIA)
Contacts & investigators
ContactJennifer McLeland, PhD · contact · mclelandj@wustl.edu · 314-747-3819
ContactLeah Taylor · contact · ltaylor24@wustl.edu · 314-747-7297
InvestigatorYo-El Ju, MD, MCSI · principal_investigator, Washington University School of Medicine
InvestigatorBrad Boeve, MD · principal_investigator, Mayo Clinic
InvestigatorRon Postuma, MD · principal_investigator, McGill University
All locations (9)
University of California Los AngelesRecruiting
Los Angeles, California, United States
Stanford UniversityRecruiting
Redwood City, California, United States
Emory UniversityRecruiting
Atlanta, Georgia, United States
Massachusetts General HospitalRecruiting
Boston, Massachusetts, United States
University of MinnesotaRecruiting
Minneapolis, Minnesota, United States
Mayo Clinic RochesterRecruiting
Rochester, Minnesota, United States
Washington University School of MedicineRecruiting
St Louis, Missouri, United States
Oregon Health Sciences UniversityRecruiting
Portland, Oregon, United States
McGill University Health Centre Research InstituteRecruiting
Montreal, Quebec, Canada