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

Sponsor
Gérond'if (Other)
Overall Status
Recruiting
CT.gov ID
NCT05561101
Collaborator
(none)
125
1
7
17.9

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Other: Caregivers burden

Detailed 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

Study Design

Study Type:
Observational
Anticipated Enrollment :
125 participants
Observational Model:
Family-Based
Time Perspective:
Prospective
Official Title:
Evolution of the Health Status of Caregivers After the Admission of Their Elderly Relative to the Emergency Department
Actual Study Start Date :
Sep 20, 2022
Anticipated Primary Completion Date :
Mar 20, 2023
Anticipated Study Completion Date :
Apr 20, 2023

Outcome Measures

Primary Outcome Measures

  1. Measure of caregiver burden by the 7-item Zarit burden scale (Mini-zarit) [1 month]

Secondary Outcome Measures

  1. Assessment of patient's level of dependence through an appreciation of instrumental activities of daily living according Lawton scale [At inclusion]

  2. Assessment of the degree of patient dependence according "Index of Independence in Activities of Daily Living" KATZ scale [At inclusion]

  3. Assessment of complications risks according Triage Risk Screening Tool score (TRST) [At inclusion]

  4. Assessment of cognitive state of elderly patients according Abbreviated Mental Test 4 score (AMT-4) [At inclusion]

    If score < 4 must search for neurocognitive disorders

  5. Assessment of commorbidity risk according Charlson score [At inclusion]

  6. Assessment of quality of life of cargivers according SF-12 score [1 month]

  7. Measure of caregiver satisfaction according Likert scale [1 month]

  8. Measure of resilience capacities acoording Brief Resilience Scale (BRS) [At inclusion]

Eligibility Criteria

Criteria

Ages Eligible for Study:
75 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Emergency Department, Bichat Hospital Paris Ile-de-France France 75018

Sponsors and Collaborators

  • Gérond'if

Investigators

  • Study Chair: PATRY Claire, MD, Extern Geriatric Mobile Team

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Gérond'if
ClinicalTrials.gov Identifier:
NCT05561101
Other Study ID Numbers:
  • 2022-A01294-39
First Posted:
Sep 30, 2022
Last Update Posted:
Jan 17, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Gérond'if
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 17, 2023