Assessment of Informal Support Provided by Caregivers at Different Stages of Alzheimer's Disease (ICAD)

Civil Hospices of Lyon

Status: Enrolling

Conditions: Alzheimer s Disease; Elderly (People Aged 65 or More); Neurocognition

Treatments: Other: " Ressources Utilisation in Dementia " (RUD) questionnaire.

Study type: Observational

Funder types: Other

Identifiers

NCT07409506

69HCL24_1258 (Other Identifier)

25-5152

Details and patient eligibility

About

In France, approximately 1,200,000 people aged 65 and over suffer from Alzheimer's disease or related disorders, of which Alzheimer's disease (AD) accounts for 70% of cases. This prevalence could double by 2050. The cognitive decline and progression to functional dependence that accompany AD are associated with a decline in quality of life, an increased risk of comorbidities, institutionalization, and mortality, as well as high care costs, placing a burden on the patient, their family and friends, and the healthcare system.

Informal care, i.e., care provided by a family member or caregiver, plays an important role in the overall management of major neurocognitive disorders (NCDs) associated with AD at home. In France, the annual cost of informal care for AD was estimated in 2008 at around €14 billion per year, or approximately 50% of the total annual cost of AD. The economic valuation of informal care serves to inform public decision-makers not only about the cost of this resource, but also about its usefulness. The issue of resource allocation (particularly the daily allowance for family caregivers - AJPA in French) at the societal level and the sharing of private (role of caregivers) and public (role of the state and local authorities) responsibilities leads us to question the determinants of this usefulness, particularly the clinical determinants in AD patients at different stages of the disease.

The main hypothesis is that informal care varies according to cognitive decline and loss of autonomy, independently or in interaction with the number and type of the patient's comorbidities, their behavioral disorders, and the caregiver's burden.

Enrollment: 312 estimated patients

Sex: All

Ages: 60+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients from Charpennes Hospital included in the MEM-AURA cohort
• Patients aged 60 years and older at inclusion
• Patients with dementia due to clinically probable Alzheimer's disease, regardless of stage
• Patients with a Mini-Mental State Evaluation (MMSE) score ≤ 26 at inclusion
• Patients accompanied by a caregiver at inclusion

Exclusion criteria

• - Patients or caregivers who have expressed their opposition to the study
• Patients living in institutions or nursing homes
• Patients protected by law (under legal protection, guardianship, or conservatorship)

Early termination Criteria :

- Patients or caregivers withdrawing their consent to participate during the study

Trial design

312 participants in 1 patient group

Patients from Charpennes Hospital

Description:

Patients from Charpennes Hospital included in the MEM-AURA cohort, accompanied by a caregiver and aged 60 years and older at inclusion with NCD due to clinically probable Alzheimer's disease and a Mini-Mental State Evaluation (MMSE) score ≤ 26 at inclusion.

Treatment:

Other: " Ressources Utilisation in Dementia " (RUD) questionnaire.