RecruitingNot ApplicableNCT03894254

Predictive Factors of Autonomy Loss in Real-life Cohort

Predictive Factors Associated With Impairment in Functional Autonomy in a Regional Real-life Cohort of Patients With Alzheimer's Disease or Related Disorders (ADRD)


Sponsor

Hospices Civils de Lyon

Enrollment

5,400 participants

Start Date

Sep 9, 2020

Study Type

INTERVENTIONAL

Conditions

Summary

The Alzheimer's disease or related disorders (ADRD) are among the most disabling diseases because of their main features such as cognitive impairment, loss of functional autonomy and behavioural disorders. In absence of current curative treatment, the identification of the predictive risk factors of progression of the disease, evaluated through its main symptoms, represents a major stake of public health. The Investigators aim at developing a regional database, which includes the patient medical records on a prospective basis, in collaboration with the medical and administrative staff and with the University hospital computer science departments. The main objective is to study the predictive factors associated with change in functional autonomy level, measured every 6 to 12 months in centres across Region Auvergne Rhone-Alpes in France. The real-life study population will consist in about 5400 patients with ADRD. The inclusion period will be of 3 years, the length of follow-up of each patient will be of 10 years max for a total study length of 13 years.


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • Patients aged 18 years and older, undergoing a medical visit in a memory center or neuro-cognition service
  • Patients living at home or in housing
  • Patients with memory impairment, at all stage of the disease

Exclusion Criteria3

  • Patients in institution
  • Patients under legal protection
  • Patients with a hearing or visual impairment, which prevents carrying out examinations

Interventions

OTHERno intervention

This is study carried out in current practice. Patients are undergoing a medical examination in a memory center, with extensive and systematic evaluations for the study involving the following tests: IADL, DAD6, New AGGIR, NPI, and mini-Zarit) assessing the functions (autonomy, behavior and caregiver burden).


Locations(5)

Hôpital Dugoujon

Caluire-et-Cuire, France

Centre Hospitalier Lyon Sud

Lyon, France

Service de neuro-cognition et neuro-ophtalmologie du Groupement Hospitalier Est

Lyon, France

CHU Saint-Etienne

Saint-Etienne, France

Centre Mémoire de Ressources et de Recherche de Lyon

Villeurbanne, France

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NCT03894254


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