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Parkinson-PEST: Preventing Emergence of Symptoms by environmental Toxicants identification

Parkinson-PEST: Preventing Emergence of Symptoms by environmental Toxicants identification - PD-PEST

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON57543
Enrollment
4500
Registered
2024-09-10
Start date
2025-08-14
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson's disease Parkinson's disease

Interventions

N.A.

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Cases: - Incident Parkinson's disease; o Defined as <=1 month since diagnosis was made by a neurologist in the Netherlands at the moment of recruitment. - Aged >=18 years; - Willing and able to provide informed written or digital consent. Controls: - Assigned an initial DBC code of one of the following specific set of diseases: o A median nerve neuropathy due to entrapment in the carpal tunnel (carpal tunnel syndrome), ulnar nerve neuropathy or compressive peroneal nerve neuropathy which is not related to a trauma or autoimmune disease; o Disc herniation (hernia); o Sciatica; o Lumbago; o Radiculopathy. - Aged >=18 years; - Willing and able to provide informed written or digital consent.

Exclusion criteria

Exclusion criteria: Cases: - Initially diagnosed in a non-participating centre and referred to one of the participating hospitals for follow-up care or a second opinion. - Other neurodegenerative diseases (e.g. atypical parkinsonism, ALS, or a  dementia subtype which is not related to PD). Controls: - Diagnosed with Parkinson's disease at the time of inclusion; - Blood relative or spouse of a case selected by the same department of neurology to prevent over matching; - Initially diagnosed elsewhere and referred to one of the participating hospitals for follow-up care or a second opinion; - Other neurodegenerative diseases (e.g. atypical parkinsonism, ALS, dementia) at time of inclusion.

Design outcomes

Primary

MeasureTime frame
The main study parameter is the difference in lifetime exposure to pesticides between cases and controls. Lifetime exposure will be estimated using complementary modalities that focus on occupational, residential, and household exposure. Exposure will be assessed using three complementary modalities: questionnaires, existing databases (residential history from the ‘personal records database’ and pesticide use database), and measurements (blood, saliva, hair, faeces, and via silicone wristbands). Furthermore, the study design allows assessment of other external factors that may be associated with the risk of PD. We will specifically quantify exposure to the following three groups of other external factors: heavy metals, solvents, and air pollution. If other potential risk factors of PD emerge during the study, we intend to also assess exposure to those factors by leveraging materials that have already been collected at baseline (if applicable) in order to answer future questions. Additionally, clinical progression of cases will be serially assessed for 36 months using an annual follow-up questionnaire. In the Nijmegen region, we will expand annual follow-up by using silicone wristbands and wrist-based sensors to assess exposure and clinical progression, respectively. Wrist-based sensors will also be worn in the Leiden region.

Secondary

MeasureTime frame
See above.

Countries

Netherlands

Contacts

Public ContactJ.S. Bogers

Radboud Universitair Medisch Centrum

jolien.bogers@radboudumc.nl(0)24 361 33 92

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Aug 9, 2026