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NCT02533739 Clinical Trial

Vestibular Disorder and Visuo-spatial Functions

Vertigo Clinical Trial

Official title:
Impact Des déficits Vestibulaires Sur le développement Des Fonctions Visuo-spatiales.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02533739
Other study ID # 2014/28MAR/143
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 2015
Est. completion date June 1, 2018

Study information
Verified date April 2019
Source Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of these studies is to determine whether vestibular disorders could affect visuo-spatial cognition. Visuo-spatial cognition will be evaluated using a new questionnaire and a new computerized test using a digital tablet in different studies.

Recruitment information / eligibility
Status Completed
Enrollment 94
Est. completion date June 1, 2018
Est. primary completion date June 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 2 Years to 99 Years
Eligibility For participants of the questionnaire study :

Participants with vertigo complaints versus participants without vertigo complaints.

For patients of the behavioural study :

Inclusion Criteria:

- Vestibular disorder (with or without vertigo)

- Deafness / hard of hearing

Exclusion Criteria:

- Neurological or psychiatric conditions

- Cochlear Implant (for functional magnetic resonance imaging study)

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Cognitive and neuropsychological assesment

Locations
Country Name City State
Belgium Cliniques universitaires Saint-Luc-UCL Bruxelles

Sponsors (1)
Lead Sponsor Collaborator
Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary Vestibular questionnaire (Newly developed to evaluate cognitive abilities) Participants will be recruited and tested within one week of recruitment. Testing will be online and will take around 20 minutes on average. The new questionnaire will evaluate demographic questions, and different cognition abilities using a likert-scale. Within one week after recruitment
Primary Standard computerized cognitive assessment (For example : Test of attentional performance, digit span, visuo-spatial span, line bisection task,...) Participants will be recruited and tested within one week of recruitment. Testing will be at the hospital and will take 2 hours maximum. Standard computerized cognitive assessment will be used such as the Test of attentional performance (TAP2.2), digit span, visuo-spatial span, line bisection task, etc. Reaction times, errors and omissions will be recorded. Within one week after recruitment
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