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Recruiting NCT05066763

Parkinson's Foundation Surveys

— Observational Parkinson Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Non-interventional.
Who it may be relevant to
Registry conditions: Parkinson Disease. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

Parkinson's Foundation Surveys is an initiative seeking to periodically survey people with Parkinson's disease (PD), their care partners and medical professionals to better understand specific aspects of living with PD.

Interventions

  • Other Non-interventional
    non-interventional

Primary outcome measures

  • Total number of survey respondents [Time frame: 10 years]

Eligibility criteria

Inclusion criteria

  • Willingness to be contacted by the Parkinson's Foundation for surveys and any future research opportunities
  • Anyone who self-reports that they have a diagnosis of Parkinson's disease
  • Care partner of a person with Parkinson's disease
  • Any health professional that regularly works with people with Parkinson's disease
  • 18 years of age or older

Exclusion criteria

  • People who report that they do not have a diagnosis of Parkinson's disease, are not a care partner to someone with PD or do not work with people with PD in the health setting
  • An individual younger than 18 years of age

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • Parkinson's Foundation — Miami

Identifiers

NCT: NCT05066763 · PF-Surveys-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗