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Active Not RecruitingNCT06391619

Huntington's Disease Young Adult Study 2.0

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
154 (actual)
Sponsor
University College, London · Academic / Other
Sex
All
Age
18 Years – 47 Years
Healthy volunteers

Summary

The goal of this observational study is to learn about the first signs of disease in young adult carriers of the gene for Huntington's disease. The main questions to answer are: * what are the earliest signs of the disease? * can we identify the best time to intervene with treatment to prevent or delay onset of symptoms? * can we identify the most reliable markers of disease for use in prevention trials? Participants will undergo the following assessments: * clinical examination * cognitive and neuropsychiatric testing * brain imaging * biofluid sampling Researchers will compare gene carriers with matched controls to see if any of these measures show evidence of early disease effects.

Detailed description

We will undertake follow up assessments of the HD-YAS cohort comprising far-from-onset premanifest mutation carriers (preHD) (n=64) and controls, matched for age, sex and education (n=67). These assessments will occur approximately 4.5 and 6 years after their baseline assessment. They will include * detailed clinical assessment * cognitive testing using CANTAB and the EMOTICOM * neuropsychiatric assessment * neuroimaging including 3T volumetric MRI, NODDI, resting state fMRI and multiparametric mapping. A subset of 20 gene carriers and 20 controls will undergo 7T imaging * blood and CSF sampling We will compare change over time in preHD and control groups and model disease burden influence (an early natural history proxy) within the preHD group. These analyses will incorporate previous baseline measurements (providing three timepoints). We will create a data-driven natural history of pathological changes across the pre-clinical period in HD and estimate longitudinal models of age and CAG-dependence on the outcomes, providing a critical tool to increase power.

Conditions

Interventions

TypeNameDescription
OTHERNo interventionStudy is observational

Timeline

Start date
2022-04-06
Primary completion
2025-12-01
Completion
2025-12-01
First posted
2024-04-30
Last updated
2024-04-30

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT06391619. Inclusion in this directory is not an endorsement.