Huntington Disease
Conditions
Keywords
Huntington's disease, HD, Huntington disease
Brief summary
The purpose of this study is to define the natural history and experiences of people who are at risk for developing Huntington's disease but who do not know their genetic status.
Detailed description
Huntington's disease (HD) is a genetic disease characterized by changes in movement and behavior. To date, little research has been done on individuals who are at risk for developing the disease. PHAROS is an observational study designed to monitor people who are at risk for developing HD, and to survey their attitudes and beliefs about their at-risk status. Investigators hope this study will help answer some important questions about HD, such as: 1.) What are the earliest signs of HD and when do they start? 2.) How accurate are the measures that physicians use in detecting the onset of HD? 3.) What factors influence the age at which a person carrying the HD gene develops the illness? and 4.) In a group of people at risk for HD, how many will develop signs of the illness over a minimum three-year period of observation? Participants in the study will be evaluated every 9 months (for 5 years) using the Unified Huntington's Disease Rating Scale (UHDRS)--a clinical tool which looks at movement, psychological and behavioral function. The participants will also be asked to complete surveys about their mood, life events, and attitudes or beliefs about being at risk for HD. A blood sample, taken at the beginning of the study, will be confidentially tested to determine if the participant has the abnormal gene for HD. Neither the participant nor any of the PHAROS physicians or coordinators will learn the results of individual gene tests. The scientists hope that this study will provide essential information for future trials of experimental drugs for HD.
Interventions
None listed
Sponsors
National Human Genome Research Institute (NHGRI)
National Institute of Neurological Disorders and Stroke (NINDS)
Huntington Study Group
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
26 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
Inclusion: * Men and women between 26-55 years of age; * Who are at risk for HD by virtue of having (or had) a parent or sibling with the illness; * Who have never been tested for the HD gene, and who do not desire to be tested for the HD gene during the duration of the study; * Agree to blinded (sample will be coded) genetic testing of the HD gene; and * Who have never been diagnosed with HD. Exclusion: Individuals Who: * have been diagnosed with HD; * are taking antipsychotic medications; * use antiemetic (anti-nausea) medications with on a regular basis (greater than 3 times per month); or * exhibit clinical signs/symptoms of psychosis at the screening visit
Countries
Canada, United States
Outcome results
None listed