Longitudinal Endpoint Assessment of Disease Burden in HD
NCT ID: NCT06475898
Last Updated: 2025-09-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
600 participants
OBSERVATIONAL
2024-06-25
2026-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Be willing and able to provide informed consent electronically;
* Self-report, when answering as a participant, that you have been diagnosed with HD by a doctor, or have undergone genetic testing and been found to carry the gene mutation responsible for HD but have not been clinically diagnosed with HD (prodromal HD);
* Have the ability to answer online questions or direct someone else to enter answers for them;
* Have the ability to ambulate independently and take care of some of your personal needs;
* Have the ability to read and understand English;
* Be willing to create a unique identifier based on personal demographic information;
* Reside in the United States or its territories. Surveys can only be completed in the US. If you move outside of the US, you will no longer be able to participate;
* Own or have access to an electronic device and secure internet connectivity
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University of Rochester Center for Health + Technology
UNKNOWN
Modality.AI, Inc
UNKNOWN
Neurotargeting LLC
INDUSTRY
Huntington Study Group
NETWORK
Responsible Party
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Principal Investigators
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Jamison Seabury
Role: PRINCIPAL_INVESTIGATOR
University of Rochester Center for Health + Technology
Locations
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Huntington Study Group
Rochester, New York, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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LEAD-HD
Identifier Type: -
Identifier Source: org_study_id
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