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Clinical Trials/NCT02189460
NCT02189460
Terminated
Not Applicable

Cognitive Mechanisms and Cerebral Substrate of Naming Impairment During Aging. Behavior and Neuroimaging Approaches.

University Hospital, Grenoble1 site in 1 country33 target enrollmentStarted: July 2014Last updated:
ConditionsCognition

Overview

Phase
Not Applicable
Status
Terminated
Sponsor
University Hospital, Grenoble
Enrollment
33
Locations
1
Primary Endpoint
Blood Oxygen Level Dependent functional MRI

Overview

Brief Summary

The purpose of this study is to understand the effect of age on language abilities. The investigators aim at investigating the cerebral modifications that take place in normal aging, at the functional an anatomical level.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
30 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Age of 30 years and above
  • Right handed
  • French native speakers
  • Affiliation to French social security (Sécurité Sociale)
  • Medical interview
  • Consent form signed

Exclusion Criteria

  • Cerebral or respiratory pathologies
  • Any MRI contrindication

Outcomes

Primary Outcomes

Blood Oxygen Level Dependent functional MRI

Time Frame: There will be a unique MRI measurement for each participant. Group analyses presentation after 1 year.

We use 3 functional tasks using block paradigm: Object naming, Verbal generation and semantic judgment, to elicit BOLD response using fMRI in order to compare functional activation patterns between subjects. We also use hypercapnic challenge to elicit BOLD response in order to obtain Cerebral Vascular Reactivity properties of subjects.

Anatomical MRI

Time Frame: There will be a unique MRI measurement for each participant. Group analyses presentation after 1 year.

We use Voxel Based Morphometry to compare cortical volume (grey matter) between subjects. We also use tractography Diffusion Tensor Imaging to compare white matter properties between subjects.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
University Hospital, Grenoble
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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