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NCT02014246 · ClinicalTrials.gov registry record

Genetic Characterization of Movement Disorders and Dementias

A clinical trial of Dementia and Movement Disorder, sponsored by National Institute on Aging (NIA).

Recruiting
Registry status
12,000
Enrollment target
1
Study location

NCT02014246: Recruiting study of Dementia and Movement Disorder, sponsored by National Institute on Aging (NIA).

NCT02014246 is a study of Dementia and Movement Disorder that is actively recruiting participants, run by National Institute on Aging (NIA). The registered enrollment target is 12,000 participants, above the 7,663-participant average among 199 other Dementia trials with a reported enrollment target (57% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02014246, a study of Dementia and Movement Disorder, is actively recruiting participants, sponsored by National Institute on Aging (NIA).

RECRUITING
Registry status
12,000 participants
Enrollment target
1
Study location

Study Summary

Background: There are two basic types of movement disorders. Some cause excessive movement, some cause slowness or lack of movement. Some of these are caused by mutations in genes. On the other hand, dementia is a condition of declining mental abilities, especially memory. Dementia can occur at any age but becomes more frequent with age. Researchers want to study the genes of families with a history of movement disorders or dementia. They hope to find a genetic cause of these disorders. This can help them better understand and treat the diseases. This study will not be limited to a particular disorder, but will study all movement disorders or dementias in general. This study will perform genetic testing to identify the genetic causes of movement disorders and dementia. Today, genetic testing can be done to analyze multiple genes at the same time. This increases the chances of finding the genetic cause of movement disorders and dementias. Objectives: To learn more about movement disorders and dementia, their causes, and treatments. Eligibility: Adults and children with a movement disorder or dementia, and their family members. Healthy volunteers. Design: Participants will be screened with medical history and blood tests. Some will have physical exam. Participants will give a blood sample by a needle in the arm. This can be done at the clinic, by their own doctor, or at home. Alternatively, a saliva sample may be provided if a blood sample cannot be obtained. Participants can opt to send an extra blood sample to a repository for future study. Genetic test will be done on these samples. The samples will be coded. The key to the code will remain at NIA. Only NIA investigators will have access to the code key. Participants can request to receive results of the tests. Participation is generally a single visit. Participants may be called back for extra

Primary Outcome

Causative for the movement disorder or dementia that the patient has been diagnosed with.

Study Locations (1)

Maryland

  • National Institute of Aging, Clinical Research Unit - Baltimore

Trial Details

FieldValue
Enrollment Target 12,000 participants
Start Date 2003-07-14
Est. Completion 2059-12-31
National Institute on Aging (NIA)

131 total trials

What NCT02014246 shows while recruiting

NCT02014246 is an observational study that tracks outcomes without assigning an intervention. Its 12,000 participants enrollment target places it among the larger protocols in the corpus, above the 7,663-participant average among 199 other Dementia trials with a reported enrollment target (57% higher).

The record links to 2 conditions, with Dementia appearing as the primary indexed condition, and to 0 interventions.

NCT02014246 reports a single indexed study location in Maryland.

Frequently Asked Questions

What is clinical trial NCT02014246 about?

NCT02014246 is a clinical study titled "Genetic Characterization of Movement Disorders and Dementias". Background: There are two basic types of movement disorders. Some cause excessive movement, some cause slowness or lack of movement. Some of these are caused by mutations in genes. On the other hand, dementia is a condition of declining mental abilities, especially memory. Dementia can occur at any...

What is the current status of trial NCT02014246?

This trial is currently recruiting. The enrollment target is 12,000 participants. The study started on 2003-07-14. Estimated completion is 2059-12-31.

What conditions does trial NCT02014246 study?

This clinical trial studies the following conditions: Dementia, Movement Disorder.

Who is sponsoring clinical trial NCT02014246?

This trial is sponsored by National Institute on Aging (NIA), which has 131 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02014246 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Dementia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02014246's enrollment target sits among peer trials

12,000 12th of 199 higher than 188 of 199 other Dementia trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Dementia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02014246, the US trial registry maintained by the National Library of Medicine. NCT02014246 (large enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.