Plain-English translation of NCT02760108 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Read our Parkinson's Disease research guide →This study invites people with Parkinson's disease—especially those diagnosed before age 45 or those with a family history—along with their relatives (affected or not) to participate in genetic research. By comparing the genes of people with Parkinson's to those without it, researchers hope to discover which genetic changes cause the disease and which may protect some people from developing it. Understanding these genetic patterns could lead to new treatments that work earlier in the disease process.
Most people with Parkinson's don't have a clear cause for their disease, but researchers believe that for some patients—particularly those diagnosed young or with affected relatives—genetic changes play a role. By studying families and identifying these genetic variations, scientists hope to develop treatments that could slow or prevent Parkinson's progression, rather than only managing symptoms after they appear.
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As a participant, you would likely provide a blood sample for genetic testing and possibly share information about your family's medical history. The study compares genetic information from people with Parkinson's, their affected relatives, and unaffected family members to identify important genetic differences. This is primarily an observational study focused on understanding genetics rather than testing a new medication.
AI-generated summary from trial data · Jun 19, 2026 · Not medical advice
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