- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04846608
Descriptive Study of Emergency Room Visits From Nursing Home Residents for Behavioral Problems at the Nancy University Hospital: Place of the Advanced Practice Nurse
November 17, 2021 updated by: Bernadette HANESSE, Central Hospital, Nancy, France
The demographic evolution of old age is a reality.
After the age of 75, 2 out of 3 people living in institutions have neurocognitive disorders.
Behavioural disorders such as physical aggression, agitation, hallucinations, sleep disorders, generate difficulties in the management of these patients and lead to unscheduled emergency hospitalizations.
Non-pharmacological management of behavioral disorders is recommended as a first-line treatment because of its low risk and potential improvement (Haute Autorité de Santé 2009).
However, this management is not simple and obvious to put in place, especially since not all elderly people with Behavioural disorders are in adapted structures.
The advanced practice nurse specializing in geriatrics has a place in this care pathway.
Because of her skills, she could "organize multi-professional care, set up analyses of practices within the nursing homes, train caregivers appropriately, and limit hospitalizations due to behavioral problems" (SALIEGE L. 2020).
Advanced practice nursing is in its infancy in France, and everything remains to be done (International Council of Nurses- directive).
The aim of the study is to identify the number of emergency room visits by people aged 75 and over for behavioral problems in nursing home during a 6 month-period.
Study Overview
Study Type
Observational
Enrollment (Actual)
4000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Nancy, France, 54000
- CHRU de Nancy
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
75 years and older (Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
All persons aged 75 and over, residents of nursing homes in the Nancy area, who consulted the emergency department during the 6 month study period
Description
Inclusion Criteria:
- Person who has received full information on the organization of the research and has not objected to the use of this data
- Elderly men and women 75 years of age and older at the time of the emergency room visit
- Having for main residence one of the nursing homes of the Grand Nancy
- Administratively present in the emergency department
Having been admitted to the emergency room for the following reasons:
- Behavioural problems
- Agitation
- Dementia
- Disorientation
- Delirium
Exclusion Criteria:
- People under 75 years of age
- Residing at home or in a senior residence or in a nursing home outside Grand Nancy
- Referred by an inpatient department (rehabilitation department)
- Other reasons for emergency room use such as "depression" and "apathy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Retrospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Nursing home residents with behavioural problems
Nursing home residents from Grand Nancy aged 75 and over referred to emergency departments for disorientation, agitation, dementia or behavioural problems during the study period
|
Observation
|
|
Nursing home residents with other problems
Nursing home residents from Grand Nancy aged 75 and over referred to emergency departments for other reasons
|
Observation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of passage of people aged 75 and over referred to emergency departments by nursing homes for disorientation, agitation, dementia or behavioural problems during the study period
Time Frame: through study completion, an average of 6 months
|
Number of passage of people aged 75 and over referred to emergency departments by nursing homes for disorientation, agitation, dementia or behavioural problems during the study period
|
through study completion, an average of 6 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Age of the patients
Time Frame: through study completion, an average of 6 months
|
through study completion, an average of 6 months
|
|
Gender of the patients
Time Frame: through study completion, an average of 6 months
|
through study completion, an average of 6 months
|
|
Presence of previous medical cognitive disorder
Time Frame: through study completion, an average of 6 months
|
through study completion, an average of 6 months
|
|
Name of nursing home of origin
Time Frame: through study completion, an average of 6 months
|
through study completion, an average of 6 months
|
|
Length of stay at emergency room
Time Frame: through study completion, an average of 6 months
|
through study completion, an average of 6 months
|
|
Referral after visit at emergency room
Time Frame: through study completion, an average of 6 months
|
through study completion, an average of 6 months
|
|
Number of iterative passage of people aged 75 and over referred to emergency departments by nursing homes for disorientation, agitation, dementia or behavioural problems during the study period
Time Frame: through study completion, an average of 6 months
|
through study completion, an average of 6 months
|
|
Presence of intervention of geriatric mobile team
Time Frame: through study completion, an average of 6 months
|
through study completion, an average of 6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 14, 2021
Primary Completion (Actual)
June 30, 2021
Study Completion (Actual)
June 30, 2021
Study Registration Dates
First Submitted
March 26, 2021
First Submitted That Met QC Criteria
April 13, 2021
First Posted (Actual)
April 15, 2021
Study Record Updates
Last Update Posted (Actual)
November 18, 2021
Last Update Submitted That Met QC Criteria
November 17, 2021
Last Verified
November 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021PI027
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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