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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06437847
Other study ID # IRBN632024/CHUSTE
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date June 2024
Est. completion date November 2024

Study information

Verified date May 2024
Source Centre Hospitalier Universitaire de Saint Etienne
Contact Angèle FOURNIER, resident
Phone (0)6.95.37.34.22
Email angele-fournier@outlook.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The prevalence of cognitive disorders is constantly increasing, with 1.2 million patients affected in France in 2016. Dementia is currently the seventh leading cause of death. In the absence of available treatment, systematic screening is not recommended. However, cognitive evaluation is recommended to maintain a level of autonomy for the patient at home. Targeted screening is the responsibility of the general practitioner. The latest recommendations from the HAS (2011) highlight the use of the MMSE as a first-line approach, there are no recommendations regarding short tests. Early cognitive assessment is limited by the time required to perform the tests and the knowledge about the available tools. The Codex is a short test, its sensitivity (92%) and specificity (85%) place it among the most discriminatory scores. It is underutilized in France. The objective of this thesis is to assess the training needs of general practitioners in short tests.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 120
Est. completion date November 2024
Est. primary completion date November 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - General practitioners of the AURA Region, in activity, university supervisor or not, trained or not trained in geriatrics. Exclusion Criteria: - General practitioners with exclusive practices in pediatrics, gynecology, aesthetics, rehabilitation, and homeopathy.

Study Design


Intervention

Other:
Questionnaire
Questionnaire assessing the use of cognitive tests.

Locations

Country Name City State
France Chu de Saint-Etienne Saint-Étienne

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Saint Etienne

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quantitative questionnaire 1 Assessment of the need to use short cognitive tests Month : 1, 3, 6
Secondary Quantitative questionnaire 2 Assessment of the expectation regarding a project of training general practitioners to use the Codex tool (Sum = 4 or 5: = CODEX normal ; Sum = 0, 1, 2 or 3 = CODEX abnormal) Month : 1, 3, 6
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