Clinical Dementia Rating Medical Record (CLIMER)

Civil Hospices of Lyon

Status: Unknown

Conditions: Clinical Dementia Rating (CDR) Face-to-face Interview With the Patient; Clinical Dementia Rating (CDR) From the Analysis of Medical Record

Treatments: Diagnostic Test: CDR assessment face-to-face

Study type: Observational

Funder types: Other

Identifiers

NCT04763941

69HCL20_0508

Details and patient eligibility

About

The assessment of severity of the cognitive and functional impairment is essential in the follow-up of patients with neurocognitive disorders and in the assessment of the effectiveness of therapeutics. However, the systematic assessment of the Clinical Dementia Rating (CDR) scale is limited due to the time required to complete it (approximately 45 min to 1 hour). Insofar as studies have shown correspondences between the CDR and scales measuring cognitive and neuropsychological performance, and as part of memory consultations, several functional and neuropsychological scales are systematically administered, we wish to conduct a study validating the feasibility of the CDR based on information already available in the patient's file compared to the evaluation of the CDR by the usual method (face-to-face interview in consultation).

This study should highlight the feasibility of scoring the CDR-SB from the files of patients in memory consultation, first in terms of reliability of the scores obtained compared to the standard evaluation, and on the other hand in terms of organization and duration of administration.

Enrollment: 144 estimated patients

Sex: All

Ages: 65+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient who has CDR assessment in face-to-face interview during the memory consultation,
• Patient with an isolated cognitive complaint or a neurocognitive disorder
• Patient included in the MEMORA cohort

Exclusion criteria

• Patient or caregiver who does not wish their data to be used for research purposes within the framework of the MEMORA cohort.

Trial design

144 participants in 1 patient group

Memory consultation patient

Description:

The study will be conducted on the basis of the patient consulting in Memory Consultation, specifically with the information already collected in normal care and the MEMORA cohort.

Treatment:

Diagnostic Test: CDR assessment face-to-face