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Clinical Trial Details — Status: Suspended

Administrative data

NCT number NCT03213119
Other study ID # 69HCL17_0263
Secondary ID 2017-A01784-49
Status Suspended
Phase N/A
First received
Last updated
Start date April 23, 2018
Est. completion date February 13, 2023

Study information

Verified date February 2023
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The exploration of space is more effective when intrinsically rewarding elements are located in the visual scene. Thus, rewards could be exploited as a novel rehabilitation approach to various attentional disorders. The first part of the project aims to characterize these effects at the behavioural level. The interventional part consists then in the administration of Caloric Vestibular Stimulation (CVS), which by means of injection of a small quantity of water in the external ear activates the vestibular organs and subsequently vestibular-related brain areas. Among the observed brain activations, the possibility to reach cingulate areas appears particularly interesting because it foreshadows the possibility to further enhance attentional capture by rewards. CVS will be delivered to patients with brain lesion of the right hemisphere, engaged in cancellation tasks requiring the processing of targets of different nature (e.g. monetary or neutral). The main prediction is that CVS administration would enhance spatial exploration in terms of center of gravity of the cancellation and improved accuracy as a function of the type of target processed (e.g. its value).


Recruitment information / eligibility

Status Suspended
Enrollment 60
Est. completion date February 13, 2023
Est. primary completion date May 8, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - More than 18 years of age, less than 85 - right handed - Benefit of social health security - Normal or corrected-to-normal vision - Brain lesion localised in the right hemisphere, confirmed by CT or MRI Exclusion Criteria: - Anamnesis of neurological of psychiatric illness - Pregnancy or breastfeeding - Administrative measures restricting legal rights - Recent participation to other brain stimulation studies (< 1 week) - Perforation of the tympanic membrane - Anamnesis of recurrent otitis media

Study Design


Related Conditions & MeSH terms

  • Brain Lesion of the Right Hemisphere
  • Unilateral Spatial Neglect for Half of Them

Intervention

Procedure:
Non-invasive brain stimulation of the vestibular system through caloric vestibular stimulation.
Caloric vestibular stimulation (CVS) involves the irrigation of cold or warm water into the external ear canal, and induces a temperature gradient across the semicircular canals stimulating the vestibular nerve. It is commonly used in both otolaryngology to assess vestibular function and neurology to test brain stem function.
Non-invasive brain stimulation of the vestibular system through caloric vestibular stimulation.
Caloric vestibular stimulation (CVS) involves the irrigation of cold or warm water into the external ear canal, and induces a temperature gradient across the semicircular canals stimulating the vestibular nerve. It is commonly used in both otolaryngology to assess vestibular function and neurology to test brain stem function.
Non-invasive brain stimulation of the vestibular system through caloric vestibular stimulation.
Caloric vestibular stimulation (CVS) involves the irrigation of cold or warm water into the external ear canal, and induces a temperature gradient across the semicircular canals stimulating the vestibular nerve. It is commonly used in both otolaryngology to assess vestibular function and neurology to test brain stem function. The SHAM condition uses body-temperature water, and thus does not result into vestibular unbalance.

Locations

Country Name City State
France CRNL, équipe IMPACT (CNRS UMR5292, INSERM U1028) Bron
France Service de médecine et réadaptation neurologique, Hôpital Henry Gabrielle Saint-Genis-Laval

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Center of Gravity (pixels). For line bisection defined as the difference between participants' mark and the objective center of the line. For cancellation tasks it is calculated as the grand average of horizontal and vertical coordinates of all the marks. In both cases smaller indices indicate a leftward exploration bias, whereas larger indices indicate rightward bias. Days 1, 2, and 3
Secondary Reaction times (ms). The speed of response is a traditional indicator of the amount of cognitive processing underneath provided responses. It is measured by professional programs (e.g. Presentation) running on standard PCs Days 1, 2, and 3.
Secondary Response accuracy (%) The proportion of correct responses provided, automatically computed by professional programs (e.g. Presentation) running on standard PCs. Days 1, 2, and 3.