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NCT04368416 Clinical Trial

Anxiety/Depression, Sleep and Alcohol in Elderly Anxiety/Depression, Sleep Disturbances and Alcohol Use Disorder in Elderly With Cognitive Complaints

Aging Clinical Trial

— MEM-ASA  

Official title:
Prevalence of Anxiety/Depression, Sleep Disturbances and Alcohol Use Disorder in Elderly With Cognitive Complaints

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04368416
Other study ID # 2019-A02928-49
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 22, 2020
Est. completion date December 31, 2024

Study information
Verified date February 2023
Source University Hospital, Caen
Contact Pierre BRANGER, MD
Phone 33231065548
Email branger-p@chu-caen.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of MEM-ASA is to investigate the prevalence of anxiety/depression, sleep disturbances and alcohol use disorder in elderly with cognitive complaints. In memory clinics of Normandy (France), all patients aged over 50 year-old are systematically questioned about anxiety, depression, sleep quality and alcohol use disorder. They also perform a neuropsychological assessment. Questionnaires are given to the patient and his/her caregiver to be filled in at home. Levels of anxiety/depression, sleep quality and alcohol consumption are related to neuropsychological performance, diagnosis and responses to the questionaires.

Recruitment information / eligibility
Status Recruiting
Enrollment 3000
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria: - To have cognitive complaints - To have french as native language - Not to be opposed to be included - To be affiliated to the social security Exclusion Criteria: -To be under tutorship or curatorship

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France University Hospital Caen

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Caen

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Anxiety and depression Responses to questions during anamnesis At inclusion
Primary Sleep quality Responses to questions during anamnesis At inclusion
Primary Alcohol use disorder Responses to questions during anamnesis At inclusion
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