NCT04394767TerminatedNot Applicable
Couple and Spouse Caregiver in Huntington's Disease
University Hospital, Lille1 site in 1 country48 target enrollmentStarted: January 13, 2020Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Terminated
- Sponsor
- Enrollment
- 48
- Locations
- 1
- Primary Endpoint
- report of the experience and interactions of couple and Spouse Caregiver in Huntington's Disease
Study Overview
Brief Summary
The objectives are to better document the psychosocial status and needs of caregiver of HD patients and understand the dyad functioning, facing the disease at various stages.
Study Design
- Study Type
- Observational
- Observational Model
- Case Only
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 30 Years to 70 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •For patient :
- •HD, CAG > 36, motor UHDRS > 5
- •Being able to communicate with the investigator
- •For both spouses :
- •Living together since at least 5 years
- •30 to 60 years old
Exclusion Criteria
- •For patient :
- •Other chronic neurologic disorder
- •For both spouses :
- •Psychiatric disease
- •Unable to participate, incl read, understand and sign the informed consent
Outcomes
Primary Outcomes
report of the experience and interactions of couple and Spouse Caregiver in Huntington's Disease
Time Frame: once time, Baseline
Qualitative assessment: Interpretative phenomenological analysis (IPA) by semi-structured interviews to explore families representations and strategies about the patients with Huntington's Disease
Secondary Outcomes
- report of the experience and interactions of couple and Spouse Caregiver in Huntington's Disease(once time, Baseline)
Investigators
Study Sites (1)
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