- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04970784
Impact of a Dedicated Geriatric Sector on the Loss of Functional Autonomy at 1 Month for Patients Admitted to Emergencies and Non-hospitalised (URG-GERIA)
Several studies have shown that going to the emergency room is a risk factor for loss of independence in the elderly. It has been shown that the period following an emergency room visit without hospitalization is a period of vulnerability for the elderly.
The functional decline, or loss of functional autonomy, of the elderly is associated with an increase in institutionalization, mortality and costs to society.
Studies have highlighted the risk factors for functional decline in the elderly, such as pre-existing functional and cognitive decline, undernutrition, but no model of care has yet prevented the risk of loss of autonomy after a stay in the emergency room.
A full and early geriatric assessment could prevent functional decline after the emergency room visit.
The primary objective of the study is to assess the impact of a dedicated geriatric sector on the functional decline at 1 month of patients admitted to emergencies without hospitalization by comparing an intervention group (patient having benefited from the geriatric sector) and a group witness ("classic" emergency patient).
The secondary objective is to evaluate the impact of this sector on the number of falls at home as well as the readmission rate within 1 month of going to the emergency room.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Contamine-sur-Arve, France
- Centre Hospitalier Alpes Léman, service des urgences
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age greater than or equal to 75 years
- Emergency room consultation between 7:30 a.m. and 5:30 p.m.
- Relevant to the adult emergency department
- Return home after consultation
Exclusion Criteria:
- Age less than 75 years
- Arrival time between 5.30 p.m. and 7.30 a.m.
- Need to take care of unhooking
- Belonging to the short sector, versatile sector
- Patients hospitalized after consultation
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Patients cared for by the adult sector
Patients admitted to emergencies, non-hospitalized and cared for by the adult sector of emergencies (classical emergencies)
|
For patients cared for by the geriatric sector, questionnaire will be filled in at admission D0 and by phone at D30, for the "classic" emergency patients questionnaire will be submitted by phone the day following the consultation D1, and D30.
|
Patients cared for by the geriatric sector
Patients admitted to emergencies, non-hospitalized and cared for by the geriatric sector of emergencies
|
For patients cared for by the geriatric sector, questionnaire will be filled in at admission D0 and by phone at D30, for the "classic" emergency patients questionnaire will be submitted by phone the day following the consultation D1, and D30.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change of functional decline at 1 month, measured by the Katz index, Activities of Daily Living (ADL)
Time Frame: At Baseline (admission to ermergencies) and 1 month
|
The Katz index, Activities of Daily Living (ADL) questionnaire, assess through 6 items (ranging from 0 to 1) the aptitude to execute daily life activities.
|
At Baseline (admission to ermergencies) and 1 month
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jessica POINTURIER, Centre Hospitalier Alpes Léman, service des urgences
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 69HCL19_0973
- 2020-A00211-38 (Other Identifier: ID-RCB)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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