Skip to main content
Clinical Trials/NCT02302482
NCT02302482
Recruiting
Not Applicable

Predictive Factors of the Autonomy Level Change Related to Memory Disorders

Hospices Civils de Lyon2 sites in 1 country10,860 target enrollmentNovember 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Memory Impairment
Sponsor
Hospices Civils de Lyon
Enrollment
10860
Locations
2
Primary Endpoint
Functional autonomy level
Status
Recruiting
Last Updated
4 years ago

Overview

Brief 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 aimed at developing a database, which includes the patient medical records on a prospective basis, in collaboration with the medical and administrative personal and with the University hospital computer science department. The main objective is to study the predictive factors associated with the change of functional autonomy level, measured every 6 months to 12 months by phone, in a Memory Clinic. The study population would consist in about 1000 patients with ADRD. The length of follow-up of each patient will be 3 years.

Registry
clinicaltrials.gov
Start Date
November 2014
End Date
November 2027
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients who undergo a medical visit in the Memory Clinic for the 1st time
  • Patients living at home or in housing
  • Patients with memory impairment, at all stage of the disease

Exclusion Criteria

  • Patients in institution
  • Patients under legal protection
  • Patients with a hearing or visual impairment, which dot not allow to carry out the examination

Outcomes

Primary Outcomes

Functional autonomy level

Time Frame: 3 years

The scores of "Lawton Instrumental Activities of Daily Living" (IADL) and of "Disability Assessment of Dementia" (DAD-6)

Secondary Outcomes

  • Cognitive function level(3 years)

Study Sites (2)

Loading locations...

Similar Trials