Scientists hunt for hidden genes behind movement disorders and dementia

NCT ID NCT02014246

Recruiting now Knowledge-focused Sponsor: National Institute on Aging (NIA) Source: ClinicalTrials.gov ↗

First seen Jun 27, 2026 · Last updated Aug 05, 2026 · Updated 8 times

Summary

This study aims to find the genetic causes of movement disorders and dementias by analyzing DNA from up to 12,000 participants, including patients and their family members. Researchers will collect blood or saliva samples and look for gene mutations linked to these conditions. The goal is to better understand the diseases, not to test any treatment. Participation typically involves a single visit.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to: If successful, this could help identify new genes linked to these conditions, pointing toward future treatments or diagnostic tests.
What could go wrong: This is an observational study, not a treatment trial. It may not find clear genetic causes, and results may take years to impact patient care.

This is an AI summary of the original study and may miss details. Read our disclaimer.

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Conditions

The condition(s) this trial relates to.

dementia movement disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

DEMENTIA MOVEMENT DISORDER

Contacts and locations

Locations

National Institute of Aging, Clinical Research Unit
RECRUITING

Baltimore, Maryland, 21224, United States

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