ClinicalTrials.Veeva

Menu

Evolution of the Health Status of Caregivers After the Admission of Their Elderly Relative to the Emergency Department (ETAP-U)

G

Gérond'if

Status

Enrolling

Conditions

Patient Without Cognitive Disorders
Caregiver-patient Dyeds

Treatments

Other: Caregivers burden

Study type

Observational

Funder types

Other

Identifiers

NCT05561101
2022-A01294-39

Details and patient eligibility

About

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

Full description

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

Enrollment

125 estimated patients

Sex

All

Ages

75+ years old

Volunteers

Accepts Healthy Volunteers

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.

Trial contacts and locations

1

Loading...

Central trial contact

DUFOUR Isabelle; LUCAS Prisca, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems