NCT07409506Recruiting
Assessment of Informal Support Provided by Caregivers at Different Stages of Alzheimer's Disease
Source: ClinicalTrials.gov · Last updated 13 Feb 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 312 (estimated)
- First submitted
- 16 Dec 2025
- Start date
- 9 Sept 2025
- Primary completion date
- 9 Sept 2026
- Lead sponsor
- Hospices Civils de Lyon
- Diseases
- Alzheimer disease
- NCT number
- NCT07409506
What you commit to
- Study type: Observational
- Planned participants: 312
- From 9 Sept 2025 to the primary completion date, 9 Sept 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- \- 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
Who the study is looking for
- 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
Age in the registry: 60 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hôpital des Charpennes Coordinator of this site? Confirm its status | Villeurbanne | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.