Ignite Creation Date:
2024-05-06 @ 3:48 PM
Last Modification Date:
2024-10-26 @ 1:57 PM
Study NCT ID:
NCT04763941
Status:
UNKNOWN
Last Update Posted:
2022-05-02
First Post:
2021-02-17
Brief Title:
Clinical Dementia Rating Medical Record
Sponsor:
Hospices Civils de Lyon
Organization:
Hospices Civils de Lyon
Study Overview
Official Title:
Reliability of the Clinical Dementia Rating Scale From the Medical Record in Comparison With the Reference Method
Status:
UNKNOWN
Status Verified Date:
2022-01
Last Known Status:
RECRUITING
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
CLIMER
Brief Summary:
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 patients 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
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
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None