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Clinical Trials/NCT04394767
NCT04394767TerminatedNot Applicable

Couple and Spouse Caregiver in Huntington's Disease

University Hospital, Lille1 site in 1 country48 target enrollmentStarted: January 13, 2020Last updated:
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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 OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

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

Sponsor
University Hospital, Lille
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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