Huntington Disease Clinical Trial
— HUNTEXPERTNCT number | NCT02218567 |
Other study ID # | 2014-A00327-40 |
Secondary ID | |
Status | Terminated |
Phase | N/A |
First received | |
Last updated | |
Start date | June 2014 |
Est. completion date | December 2015 |
Verified date | June 2014 |
Source | University Hospital, Angers |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The study hypothesis is that caregivers experience allows them to develop a lot of knowledge and know-how about behavioural problems in Huntington Disease and its consequences. The purpose of this study is to collect, describe and analyse caregivers experience in order to find and enhance their knowledge related to the adaptation to behavioural problems of Huntington Disease patients.
Status | Terminated |
Enrollment | 12 |
Est. completion date | December 2015 |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - For patients: - Patients with Huntington Disease declared - Huntington Disease diagnosed with abnormal number of CAG repeats: 38 < nucleotide expansion (CAG) - Total Functional Capacity = 7 - Patients living with a caregiver - Aged 18 years and above - Subject gave its written consent - For caregivers : - No risk of caregiver having Huntington disease - Aged 18 years and above - Subject gave its written consent Exclusion Criteria: - For patients: - Patient who do not live with a caregiver - No national health insurance affiliation - Being under guardianship - For caregivers : - Caregiver at risk for Huntington Disease - No national health insurance affiliation - Being under guardianship |
Country | Name | City | State |
---|---|---|---|
France | University Hospital of Angers | Angers | Maine Et Loire |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Angers |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The Huntington's Disease health-related Quality of Life questionnaire | The primary outcome is to find a list of caregiver competences necessary to prevent and adapt to behavioural problems of Huntington Disease patients. | Baseline |
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