Behavioural Problems in Huntington Disease : Analysis and Enhancement of Caregiver and Patient Experience (HUNTEXPERT)
Primary Purpose
Huntington Disease
Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
questionnaire qualilty of life
psychological interview
psychological tests
Motor evaluation
Behavioral evaluation
cognitive tests
Sponsored by
About this trial
This is an interventional supportive care trial for Huntington Disease
Eligibility Criteria
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
Sites / Locations
- University Hospital of Angers
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
Patients
Caregivers
Arm Description
Outcomes
Primary Outcome Measures
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.
Secondary Outcome Measures
Full Information
NCT ID
NCT02218567
First Posted
August 14, 2014
Last Updated
October 20, 2020
Sponsor
University Hospital, Angers
1. Study Identification
Unique Protocol Identification Number
NCT02218567
Brief Title
Behavioural Problems in Huntington Disease : Analysis and Enhancement of Caregiver and Patient Experience
Acronym
HUNTEXPERT
Study Type
Interventional
2. Study Status
Record Verification Date
June 2014
Overall Recruitment Status
Terminated
Why Stopped
inclusion difficult
Study Start Date
June 2014 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Angers
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Huntington Disease
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Patients
Arm Type
Other
Arm Title
Caregivers
Arm Type
Other
Intervention Type
Behavioral
Intervention Name(s)
questionnaire qualilty of life
Intervention Type
Behavioral
Intervention Name(s)
psychological interview
Intervention Type
Behavioral
Intervention Name(s)
psychological tests
Intervention Type
Other
Intervention Name(s)
Motor evaluation
Intervention Type
Behavioral
Intervention Name(s)
Behavioral evaluation
Intervention Type
Behavioral
Intervention Name(s)
cognitive tests
Primary Outcome Measure Information:
Title
The Huntington's Disease health-related Quality of Life questionnaire
Description
The primary outcome is to find a list of caregiver competences necessary to prevent and adapt to behavioural problems of Huntington Disease patients.
Time Frame
Baseline
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Facility Information:
Facility Name
University Hospital of Angers
City
Angers
State/Province
Maine Et Loire
ZIP/Postal Code
49933
Country
France
12. IPD Sharing Statement
Learn more about this trial
Behavioural Problems in Huntington Disease : Analysis and Enhancement of Caregiver and Patient Experience
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