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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05182879
Other study ID # 2016_23
Secondary ID 2016-A01750-51
Status Recruiting
Phase
First received
Last updated
Start date February 12, 2019
Est. completion date March 2025

Study information

Verified date January 2023
Source University Hospital, Lille
Contact Nassir MESSADI, PhD
Phone 3 20 86 06 50
Email nassir.messaadi@univ-lille.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Evaluate the sensitivity of the GERONTOPOLE scale, used by general practitioners in primary care outpatients for the diagnosis of frailty in non-dependent people more than 65 years old, using as reference the "évaluation gériatrique standardisée clinique" (EGS)


Recruitment information / eligibility

Status Recruiting
Enrollment 740
Est. completion date March 2025
Est. primary completion date March 2025
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - Independent patients Exclusion Criteria: - Dependent outpatient, assessed with a "activity of daily living" (ADL) score < 6/6 - outpatient with occuring severe health episode less than a month before inclusion

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Assessement with GERONTOPOLE scale
The practitionner assesses the frailty of the elderly outpatient with the GERONTOPOLE scale and compares it with the "évaluation gériatrique standardisée" (GDS)

Locations

Country Name City State
France CHU Lille Lille Nord

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary assess the sensitivity of the GERONTOPOLE scale by practitionner 2 years
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