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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04616287
Other study ID # 7942
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 25, 2021
Est. completion date December 2023

Study information

Verified date August 2023
Source University Hospital, Strasbourg, France
Contact Nathalie PHILIPPI, MD
Phone 03 88 12 86 31
Email nathalie.philippi@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The present project aims at exploring different components of Self-consciousness or 'the Self', such as autobiographical memory, self-concept and subjective sense of Self, in dementia with Lewy Bodies (DLB) compared to Alzheimer's disease and to normal ageing. Anatomical substrates will be studied in multimodal imaging, in terms of volume, anatomical and functional connectivity. We expect to find an alteration of the different components of the Self, consecutive to insular dysfunction, a key region within cerebral networks of self-consciousness, which is damaged early in the course of the disease.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date December 2023
Est. primary completion date October 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 60 Years to 80 Years
Eligibility Inclusion Criteria: Inclusion criteria for all participants: - Male or female aged between 60 to 80, at the inclusion visit - Right-handed - Must be affiliated to a social health insurance protection scheme - Must be able both to understand the objectives and risks related to the study and to give a dated and signed informed consent - Fluency in French - At least 9 years of formal education Inclusion criteria for group of dementia with Lewy bodies: - Subject meeting McKeith et al. criteria (2017) - Subject with prodromal dementia with Lewy bodies meeting the DSM-V Mild Cognitive Impairment criteria (2013) - Subject with prodromal or mild dementia with Lewy bodies with an = 20 MMSE score - Availability of a caregiver for the inclusion visit Inclusion criteria for group of Alzheimer disease: - Subject meeting Dubois et al. criteria (2014) - Subject with prodromal or mild Alzheimer disease with an = 20 MMSE score - Availability of a caregiver for the inclusion visit Inclusion criteria for healthy elderly: - Subject must be matched with patients in terms of age, gender and educational level - Absence of any cognitive complaint - Autonomy must be preserved Exclusion Criteria: Subjects with significant neuropsychiatric comorbidities - Abnormal neurological examination - Sensory impairment that may significantly interfere with testing - Contraindication to MRI - Claustrophobia - Heavy psychotropic drug treatment - Excessive and regular consumption of alcohol - Subject in period of exclusion (determined by a previous or ongoing study) - Inability to give the subject informed information - Subject under judicial protection - Subject under tutorship or guardianship

Study Design


Intervention

Other:
Neuropsychological assessment and Multimodal brain MRI
Neuropsychological assessment and Multimodal brain MRI

Locations

Country Name City State
France Hôpitaux Universitaires de Strasbourg Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Neuropsychological assessment months 3
Primary Multimodal brain MRI months 3
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