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NCT02302482 Clinical Trial

Predictive Factors and Autonomy Level Change

Memory Impairment Clinical Trial

— MEMORA  

Official title:
Predictive Factors of the Autonomy Level Change Related to Memory Disorders

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02302482
Other study ID # 2014.868
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 2014
Est. completion date November 2027

Study information
Verified date June 2021
Source Hospices Civils de Lyon
Contact Pierre Krolak-Salmon, Professor
Phone (0)4 72 43 20 50
Email pierre.krolak-salmon@chu-lyon.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The Alzheimer's disease or related disorders (ADRD) are among the most disabling diseases because of their main features such as cognitive impairment, loss of functional autonomy and behavioural disorders. In absence of current curative treatment, the identification of the predictive risk factors of progression of the disease, evaluated through its main symptoms, represents a major stake of public health. The investigators aimed at developing a database, which includes the patient medical records on a prospective basis, in collaboration with the medical and administrative personal and with the University hospital computer science department. The main objective is to study the predictive factors associated with the change of functional autonomy level, measured every 6 months to 12 months by phone, in a Memory Clinic. The study population would consist in about 1000 patients with ADRD. The length of follow-up of each patient will be 3 years.

Recruitment information / eligibility
Status Recruiting
Enrollment 10860
Est. completion date November 2027
Est. primary completion date November 2027
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - Patients who undergo a medical visit in the Memory Clinic for the 1st time - Patients living at home or in housing - Patients with memory impairment, at all stage of the disease Exclusion Criteria: - Patients in institution - Patients under legal protection - Patients with a hearing or visual impairment, which dot not allow to carry out the examination

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• The Lawton Instrumental Activities of Daily Living score (IADL), and the disability assessment of dementia score (DAD-6

Locations
Country Name City State
France Hôpital Dugoujon Caluire-et-Cuire
France Hospices Civils de Lyon - Hôpital des Charpennes Lyon

Sponsors (1)
Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Functional autonomy level The scores of "Lawton Instrumental Activities of Daily Living" (IADL) and of "Disability Assessment of Dementia" (DAD-6) 3 years
Secondary Cognitive function level Mini Mental Test examination (MMSE) 3 years
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