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Assessment of the Psychological, Cognitive and Social Resources of Applicants for Huntington's Disease and Presymptomatic Genetic Testing (PREHUNT)

U

University Hospital, Angers

Status

Completed

Conditions

Presymptomatic Huntington Disease

Treatments

Radiation: MRI
Other: neurological tests
Behavioral: psychological interview
Other: cognitive tests

Study type

Interventional

Funder types

Other

Identifiers

NCT02134561
2013-A00088-37

Details and patient eligibility

About

The purpose of this study is to assess the psychological, cognitive and social resources of applicants for Huntington's Disease and Presymptomatic Testing.

Enrollment

24 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Applicants for Huntington's Disease and Presymptomatic Testing
  • Aged 18 years and above
  • Huntington disease family member
  • Subject gave its written consent

Exclusion criteria

  • No national health insurance affiliation
  • Being under guardianship
  • Meeting brain MRI exclusion criteria (pacemakers, aneurysm clips, artificial heart valves, ear implants, metal fragments or foreign objects in the eyes, skin, or body, Renal failure, hypersensitivity of Gadolinium) or refusing MRI.
  • Patient with movement disorder

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

24 participants in 1 patient group

All subjects
Other group
Description:
psychological interview, MRI, neurological tests, cognitive tests
Treatment:
Behavioral: psychological interview
Other: neurological tests
Radiation: MRI
Other: cognitive tests

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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