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Building a detailed picture of Parkinson's

This study combines body samples, skin measures, treatment information and thinking assessments to investigate differences between people.

Learning by observing or collecting information · Study reference: NL-OMON54513

Plain-language introduction written with AI from the registry; not independently checked by a clinician. Read the original details below ↓

This registry record was last updated over six months ago, or its update date is missing. Recruitment may have changed. Confirm with the team before making plans.

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Looking for volunteers

Start (reported date)
2021-07-29

Planned dates can move. A study finishing does not tell us when a paper will be published.

No results summary has been confirmed in the registry records we imported. See connected papers below; we keep checking after recruitment ends.

Changes we have recorded
  • 2026-10-11 — recruiting

These are dates we observed a change, not necessarily the dates it happened.

Papers connected to this study

No connected paper has been found yet. The tracker checks the growing library for study identifiers and registry-linked publications.

Who can join?

Ages 18 to 99 · Ask the team who can join

These are starting points, not the full rules. The research team can tell you whether the study is right for your situation.

Read all the rules for taking part

Sex eligibility reported by registry: Not reported

Inclusion criteria: Prior to enrollment in this clinical investigation, candidates must meet ALL of the following criteria: Patients: • recently diagnosed with PD (N=625; time since Parkinson diagnosis 2 & 65 years) in both patient groups, will be attempted. • 18 years or older; • able to read and speak Dutch • Providing IRB-approved Informed Consent; • Willing, competent and able to comply with all aspects of the protocol, including follow-up schedule and biospecimen collections. Controls: • 18 years or older • Healthy (Self-report) • Is able to read and speak Dutch • Even distribution with respect to gender and age of the patient groups will be attempted • Providing IRB-approved Informed Consent; • Willing, competent and able to comply with all aspects of the protocol, including follow-up schedule and biospecimen collections. Exclusion criteria: Patients • Patients who received brain surgery for Parkinson*s disease, patients who currently use levodopa continuous intestinal gel or patients who are currently receiving apomorphine treatment. • presence of co-morbidities that would hamper interpretation of parkinsonian disability, in the opinion of the lnvestigator. • MoCa score of <=16 (indicates dementia) • Unwillingness to be informed of unexpected medical findings Controls • A history of neurological disorders that affect the brain or central nervous system • Abnormal findings at general neurological examination • Unwillingness to be informed of unexpected medical findings
Full study name & original research details

Official study title

Profiling Parkinson's disease - ProPark

Short title used by the registry

Profiling Parkinson's disease

Original description

Primary outcome: main study parameters are biomarker concentrations (i.e. blood, CSF & feces), skin alpha-synuclein (a-syn) aggregation, ADR occurrence and cognition scores. Secondary outcome: nvt

Conditions reported: Parkinson Parkinson's disease;10028037

Registry records for this study

Records are joined using registration identifiers. Titles alone do not establish that two studies are the same.

Study type
Observational
Interventions
Not reported
Phases
Not reported
Sponsor
Vrije Universiteit Medisch Centrum
Start date reported by registry
2021-07-29 (reported)

Registry updated: Not reported · Status last verified by the registry submitter: Not reported

Registry records retrieved 2026-10-13 (UTC). Individual records may have older updates. Recruitment and eligibility must be confirmed with the study team.

Contact the research team

Public study contacts supplied to the registry. Ask whether recruitment is still open and what participation involves.

Study locations

Site status can differ from overall study status. “Status not reported” means local availability needs confirmation. Remote participation and travel arrangements must be checked with the team.

Facility not reported

Netherlands

Status not reported

The original descriptions and participation rules come from the registry. Participation is voluntary and does not guarantee benefit.