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

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02134561

Acronym

PREHUNT

Enrollment

Registered

2014-05-09

Start date

2013-09-30

Completion date

2018-08-31

Last updated

2020-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Presymptomatic Huntington Disease

Brief summary

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

Interventions

BEHAVIORALpsychological interview

RADIATIONMRI

This MRI is a specific intervention assign to the subjects of the study, that's why it is an interventionnal study

OTHERcognitive tests

OTHERneurological tests

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

SUPPORTIVE_CARE

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

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

Design outcomes

Primary

Measure	Time frame
Change from baseline total score of the psychological Unified Huntington's Disease Rating Scale at 2 years	3 months before diagnostic (baseline) ; 2 years after diagnostic,

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026