Robustness Predictive Factors in People Aged Over 75 Years After Going to the Emergency Room (ROB-U)

NCT ID: NCT04683380

Last Updated: 2022-01-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

110 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-03-10

Study Completion Date

2021-12-10

Brief Summary

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After emergency room visits, the elderly patients can increase their dependence and functional decline. In this context the goal of this study is to demonstrate that there are robustness predictive factors after visit to the emergency room.

Detailed Description

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The emergency department is one of the main access routes to the hospital for elderly patients.

Older age is often associated with an increase risk of longer stay in the emergency room with a high subsequent risk of hospital re-admission. One of the essential care objectives when treating these patients is to maintain the autonomy to avoid any dependence in order to keep the quality of life, and limit the time of hospitalization.

Emergency room visits and hospitalizations are too often considered as a source of autonomy loss aggravation in the elderly. Many studies have demonstrated the mortality predictive factors existence, functional decline, or re-hospitalization of the elderly after an emergency room visit or after hospitalization.

No study until now has investigated the existence of factors directly predictive of robustness. Then the goal of this study is to demonstrate that there are robustness predictive factors after going to the emergency room.

Conditions

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Aging Emergency Room Risk Factors

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Patients admitted to the emergency room
* Patients aged ≥ 75 years old
* Patients without cognitive disorders or vigilance disorders
* Patients living at home
* Patients able to give its non-opposition


* Patients admitted to the hospital in the last 3 months
* Patients refusing to participate in the study

Exclusion Criteria

* Patients whose stay is \< 14h or \> 48h
* Patients who die during hospitalization
* Patient not hospitalized
* Patient not returning home after discharge from hospital
Minimum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Lille Catholic University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jean Bouquillon

Role: PRINCIPAL_INVESTIGATOR

Hôpital Saint-Vincent de Paul

Locations

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Saint-Vincent Hospital

Lille, Haut-de-France, France

Site Status

Countries

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France

Other Identifiers

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RC-P0099

Identifier Type: -

Identifier Source: org_study_id

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