NCT05182879

Terminated

Evaluation of Frail Elderly in Ambulatory Primary Care

University Hospital, Lille Source

ClinicalTrials.gov

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Other study identifiers

Sponsor study identifier

2016_23

Secondary identifiers

2016-A01750-51

OTHER · ID-RCB number, ANSM

Study Type

observational

Actual enrollment (reported)

36

Locations

1 country

Sites

1

Timeline

Study Start

February 12, 2019

Actual (reported)

Primary Completion

January 1, 2026

Actual (reported)

Study Completion

January 1, 2026

Actual (reported)

Brief 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)

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: terminated
Actual enrollment (reported): 36 participants
Study completion date: January 1, 2026
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

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Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
February 12, 2019
Actual (reported)
First Submitted
December 22, 2021
Actual (reported)
First Posted
January 10, 2022
Actual (reported)
Primary Completion
January 1, 2026
Actual (reported)
Study Completion
January 1, 2026
Actual (reported)

Last Updated: May 22, 2026
Status Verified: May 2026
Last Update Submitted: May 20, 2026

Conditions

Frailty

Outcome Measures

Primary Outcomes (1)

assess the sensitivity of the GERONTOPOLE scale
by practitionner
2 years

Interventions

Assessement with GERONTOPOLE scaleDiagnostic test

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

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age65 Years+

Sexall

Healthy VolunteersNo

Age GroupsOlder Adult (65+)

Sampling MethodProbability Sample

Study Population

Elderly independent population

You may qualify if:

Independent patients

You may not qualify if:

Sponsors & Collaborators

University Hospital, Lille
Otherlead

Study Sites (1)

CHU Lille

Lille, Nord, 59000, France

MeSH Terms

Conditions

Frailty

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

Nassir MESSAADI, PhD
University Hospital, Lille
PRINCIPAL INVESTIGATOR

Enrollment

36 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: OTHER
Time Perspective: CROSS SECTIONAL
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

December 22, 2021

First Posted

January 10, 2022

Study Start

February 12, 2019

Actual (reported)

Detection, Evaluation and Monitoring of Frailties in the Elderly (FRAGING)

Not ApplicableUnknown

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Not ApplicableTerminated

NCT05742737

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Completed

NCT04206904

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Completed

Dependent outpatient, assessed with a "activity of daily living" (ADL) score \< 6/6

Contact the study team to confirm eligibility.

Primary Completion

January 1, 2026

Actual (reported)

Study Completion

January 1, 2026

Actual (reported)

Last Updated

May 22, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing: Will not share

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT05182879
Data provider: ClinicalTrials.gov
Source updated: 2026-05-22
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:36:18 UTC

Locations

FR(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (1)

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

Data Sharing

Source record

Locations