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
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.
UNKNOWN
125 participants
OBSERVATIONAL
2022-09-20
2024-04-20
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Geriatric Transitional Care for Older Patients Discharged From the Emergency Department: Impact on Early Readmissions
NCT05814328
Urgent Care for the Elderly: Impairment and Home Care Services
NCT02900391
Impact of a Dedicated Geriatric Sector on the Loss of Functional Autonomy at 1 Month for Patients Admitted to Emergencies and Non-hospitalised
NCT04970784
MEMORA-Caregiver : Risk Factors of Caregiver Burden Among Patients With Neurocognitive Disorders or Subjective Cognitive Complaint
NCT02825732
Cohort of Patients with Alzheimer's Disease and Their Families.
NCT05516667
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
FAMILY_BASED
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
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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.
75 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Gérond'if
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
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
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
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.