Effect of Normal Aging on Language Processing (SEMVIE)

October 9, 2018 updated by: University Hospital, Grenoble

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

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 Overview

Status

Terminated

Conditions

Study Type

Observational

Enrollment (Actual)

33

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Grenoble, France, 38000
        • IRMaGe facility

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

30 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

60 healthy adults will participate to the study. There will be 3 age groups: 30-50, 50-70, > 70 years. Ech group will contain 20 volunteers.

The volunteers are recruited by means of ads on Laboratory websites and Universities.

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Other
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Healthy adults
20 young adults aged between 30 and 50 years old. 20 middle aged adults aged between 50 and 70 years old. 20 older adults of 70 years old and more.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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.

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

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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Alexandre Krainik, Professor, Neuroradiology department, Grenoble Hospital, INSERM, Grenoble University.
  • Study Director: Monica Baciu, Professor, Laboratory of Psychology and NeuroCognition, CNRS, Grenoble University.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2014

Primary Completion (Actual)

July 1, 2018

Study Completion (Actual)

July 1, 2018

Study Registration Dates

First Submitted

July 3, 2014

First Submitted That Met QC Criteria

July 10, 2014

First Posted (Estimate)

July 14, 2014

Study Record Updates

Last Update Posted (Actual)

October 12, 2018

Last Update Submitted That Met QC Criteria

October 9, 2018

Last Verified

October 1, 2018

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 2014-AZ00569-38

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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