Evolution of the Health Status of Caregivers After the Admission of Their Elderly Relative to the Emergency Department

NCT ID: NCT05561101

Last Updated: 2023-03-01

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

125 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-09-20

Study Completion Date

2024-04-20

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The main objective of this non-interventional, propective and multipercentric study is to Assess the evolution of caregiver burden 1 month after their elderly relative's Emergency Department (ED) admission

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The aim purpose of this non-interventional, prospertive study is to compare the evolution of caregiver burden between inclusion and 1month after their elderly relative's ED admission.

Inclusion of caregivers - patients dyads, meeting inclusion criteria and agreeing to participate, is carried out by geriatric mobile teams (EMG) working within Emergengy Department.

At inclusion the following data will be collected:

For the patient :

* Presence of neurocognitive disorders
* Sociodemographic data (age, gender, lifestyle)
* Patient comorbidities
* Autonomy and independence
* Risk of early readmission and loss of autonomy

For the caregiver:

* Socio-demographic data
* The caregiver's burden
* Quality of life
* Resilience capacity will be measured

The follow-up of the caregiver is carried out 1 month after the passage of his elderly relative to Emergency Department (at inclusion). The levels of burden and quality of life as well as the aids set up at home will be collected

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Caregiver-patient Dyeds Patient Without Cognitive Disorders

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

FAMILY_BASED

Study Time Perspective

PROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Caregivers burden

Assessment of caregiver burden after admision at Emergency Department of their elderly relative

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Adult caregivers - patients aged 75 and over dyads consulting in Emergency Department and living at home
* Patients admitted to the emergency department for less than 48 hours for which a return home is decided
* Non-verbal opposition of the patient and caregiver to the collection of their data.

Exclusion Criteria

* Hospitalized patient after emergency
* Patient admitted to emergency for life-saving emergency
* Patient living Nursing Home (EHPAD)
* Language barrier
* Absence of identified caregivers
* Severe cognitive impairment as per Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria and absence relative at time of inclusion
* Patients under guardianship
* Oral opposition from the patient and caregiver to their data collection.
Minimum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Gérond'if

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

PATRY Claire, MD

Role: STUDY_CHAIR

Extern Geriatric Mobile Team

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Emergency Department, Bichat Hospital

Paris, Île-de-France Region, France

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

France

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

DUFOUR Isabelle

Role: CONTACT

+33 (0) 185781010

LUCAS Prisca, PhD

Role: CONTACT

+33 (0) 185781010

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

PATRY Claire, MD

Role: primary

+33(0)153111818

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2022-A01294-39

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.