Enroll -HD: A Prospective Registry Study in a Global Huntington's Disease Cohort
Condition(s) studied
Study summary
Enroll-HD is a longitudinal, observational, multinational study that integrates two former Huntington's disease (HD) registries-REGISTRY in Europe, and COHORT in North America and Australasia-while also expanding to include sites in Latin America. More than 30,000 participants have now enrolled into the study. With annual assessments and no end date, Enroll-HD has built a large and rich database of longitudinal clinical data and biospecimens that form the basis for studies developing tools and biomarkers for progression and prognosis, identifying clinically-relevant phenotypic characteristics, and establishing clearly defined endpoints for interventional studies. Periodic cuts of the database are now available to any interested researcher to use in their research - visit www.enroll-hd.org/for-researchers/access-data/ to learn more.
Eligibility
Primary outcome measure(s)
- Motor Assessments: Unified Huntington's Disease Rating Scale (UHDRS) 99 Motor, UHDRS '99 Diagnostic Confidence Level — through study completion, an average of 1 year
The motor section of the UHDRS assesses motor features of HD with standardized ratings of oculomotor function, dysarthria, chorea, dystonia, gait, and postural stability. UHDRS 99 Motor, UHDRS Diagnostic Confidence Level. - Functional Assessments: UHDRS '99 Total Functional Capacity, UHDRS '99 Functional Assessment Scale, UHDRS '99 Independence Scale — through study completion, an average of 1 year
The Total Functional Capacity, Functional Assessment and Independence Subscales of the UHDRS '99 will be used to assess participants' functional status. The Total Functional Capacity scale has established psychometric properties including inter-rater reliability and validity, based on radiographic measures of disease progression. - Problem Behaviors Assessment-Short (PBA-s) — through study completion, an average of 1 year
The Problem Behavioral Assessment Short Version (PBA-s) will be used to perform behavioral assessments. This instrument measures frequency and severity of symptoms related to altered affect, thought content and coping styles. - Cognitive Assessments: Symbol Digit Modality Test; Stroop Color Naming; Stroop Word Reading; Categorical Verbal Fluency — through study completion, an average of 1 year
Cognition will be assessed using the Categorical Verbal Fluency Test, Symbol Digit Modality Test and Stroop Color and Word Reading Test. Verbal fluency is a commonly used neuropsychological test which examines the ability to spontaneously produce words orally within a fixed time span. For category fluency, words must be produced according to semantic constraints. The measure of performance used will be the number of correctly generated words within 60 seconds.
Trial sites (183)
| Facility | City | Region | Status |
|---|---|---|---|
| University of Alabama | Birmingham | Alabama | Recruiting |
| St. Joseph's Hospital and Medical Center | Phoenix | Arizona | Recruiting |
| University of California - Irvine Medical Center | Irvine | California | Recruiting |
| Loma Linda Medical Center | Loma Linda | California | Terminated |
| University of California - Los Angeles | Los Angeles | California | Recruiting |
| University of California - Davis | Sacramento | California | Recruiting |
| University of California - San Diego | San Diego | California | Recruiting |
| University of California - San Francisco | San Francisco | California | Recruiting |
| Cenexel Rocky Mountain Clinical Research, LLC | Englewood | Colorado | Recruiting |
| University of Connecticut | Farmington | Connecticut | Recruiting |
| Georgetown University | Washington D.C. | District of Columbia | Recruiting |
| University of Florida Board of Trustees | Gainesville | Florida | Recruiting |
| University of Miami | Miami | Florida | Recruiting |
| University of South Florida, HDSA Center of Excellence at USF | Tampa | Florida | Recruiting |
| Emory University, Wesley Woods Health Center | Atlanta | Georgia | Recruiting |
| Georgia Health Sciences University | Augusta | Georgia | Terminated |
| Northwestern University | Chicago | Illinois | Recruiting |
| University of Chicago | Chicago | Illinois | Terminated |
| Rush University Medical Center | Chicago | Illinois | Recruiting |
| University of Illinois College of Medicine at Rockford | Rockford | Illinois | Terminated |
| Indiana University | Indianapolis | Indiana | Recruiting |
| University of Iowa | Iowa City | Iowa | Recruiting |
| University of Kansas Medical Center | Kansas City | Kansas | Recruiting |
| Hereditary Neurological Disease Center | Wichita | Kansas | Recruiting |
| University of Louisville | Louisville | Kentucky | Recruiting |
| University of Maryland School of Medicine | Baltimore | Maryland | Withdrawn |
| Johns Hopkins University | Baltimore | Maryland | Recruiting |
| Boston University Medical Center | Boston | Massachusetts | Terminated |
| Beth Israel Deaconess Medical Center | Boston | Massachusetts | Recruiting |
| University of Michigan | Ann Arbor | Michigan | Recruiting |
| Wayne State University | Detroit | Michigan | Withdrawn |
| Hennepin County Medical Center | Minneapolis | Minnesota | Recruiting |
| Washington University in St. Louis | St Louis | Missouri | Recruiting |
| University of Nebraska Medical Center | Omaha | Nebraska | Recruiting |
| Cleveland Clinic - Las Vegas | Las Vegas | Nevada | Recruiting |
| Cooper University Hospital | Camden | New Jersey | Active Not Recruiting |
| Rutgers, the State University of New Jersey | New Brunswick | New Jersey | Recruiting |
| Albany Medical College | Albany | New York | Recruiting |
| Columbia University | New York | New York | Recruiting |
| University of Rochester | Rochester | New York | Recruiting |
+ 143 more sites — see the full list on the official registry below.
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT01574053 on ClinicalTrials.gov ↗ ← All trials in Italy