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EEG Classification System for Dementia

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ClinicalTrials.gov Identifier: NCT02273921
Recruitment Status : Enrolling by invitation
First Posted : October 24, 2014
Last Update Posted : October 24, 2014
Sponsor:
Collaborator:
Landspitali University Hospital
Information provided by (Responsible Party):
Mentis Cura

Brief Summary:

The goal of this study is to construct a large database of EEG recordings from elderly individuals in predefined groups. The purpose of this database is to select groups of EEG recordings from the database in order to compare the electrophysiology, as measured by EEG, of the groups.

In the clinical trial part all individuals are treated exactly the same and are therefore considered a single group. The categorization is performed during the data analysis.

The groups in the data analysis will initially be based on the following:

  1. Healthy controls
  2. Mild Cognitive Impairment
  3. Alzheimers Disease (AD)
  4. Lewy-body Dementia
  5. Parkinsons Disease Dementia
  6. Vascular Dementia (VaD)
  7. Frontotemporal Dementia (FTD)
  8. Depression

Other groups will be added if needed.


Condition or disease Intervention/treatment Phase
Dementia Other: EEG recording Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 2000 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: EEG Classification System for Dementia
Study Start Date : March 2005
Estimated Primary Completion Date : June 2020
Estimated Study Completion Date : June 2020

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Dementia

Arm Intervention/treatment
No Intervention: EEG
A non-invasive EEG recording
Other: EEG recording
EEG is recorded once for each participant




Primary Outcome Measures :
  1. Classification system for dementia based on EEG [ Time Frame: The quality of the classification system will be evaluated regularly, at least every 6 months, up to 6 years. ]
    The EEGs recorded in the trial will be categorized into controls or predefined clinical groups based on the participants' clinical diagnosis. The classification system will be constructed using this categorization.



Information from the National Library of Medicine

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Ages Eligible for Study:   50 Years to 90 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Age of participant in the range of 50-90 years

Exclusion Criteria:

  • Outside required age range

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02273921


Sponsors and Collaborators
Mentis Cura
Landspitali University Hospital
Investigators
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Principal Investigator: Jón Snædal, MD Landspitali University Hospital

Publications of Results:
Other Publications:
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Responsible Party: Mentis Cura
ClinicalTrials.gov Identifier: NCT02273921     History of Changes
Other Study ID Numbers: MC-CT-002
First Posted: October 24, 2014    Key Record Dates
Last Update Posted: October 24, 2014
Last Verified: October 2014
Keywords provided by Mentis Cura:
Dementia, Diagnosis, Electroencephalography
Additional relevant MeSH terms:
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Dementia
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Neurocognitive Disorders
Mental Disorders