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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03508024
Other study ID # NI_2016_39
Secondary ID 2017-A00486-47
Status Completed
Phase
First received
Last updated
Start date January 5, 2018
Est. completion date April 25, 2019

Study information

Verified date April 2018
Source University Hospital, Lille
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to determine factors related to diagnosis delay for patients with young onset dementia (first symptoms before 60 years old) who live in North of France.


Recruitment information / eligibility

Status Completed
Enrollment 220
Est. completion date April 25, 2019
Est. primary completion date April 25, 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: As part of this study, patients will be considered: - Residing in the departments of Nord (59) and Pas-de-Calais (62), - whose diagnosis of Alzheimer's disease or related illness (DLFT, DCL) was made and announced, - Whose diagnosis of illness was made after 2007 - whose first symptoms appeared before the age of 60 Patients included in the COMAJ cohort and those who completed the Pathways medical and social booklet will have to meet these criteria to be selected for this study. As part of the survey, caregivers of patients meeting the above criteria and the following two will be recruited: - Having consulted or being followed by liberal neurologists or in hospital memory consultations (excluding CMRR-CNR-MAJ Lille) of the departments of Nord and Pas-de-Calais, - Not monitored at the CMRR-CNR-MAJ Lille (ad hoc notice possible). The caregiver is defined as a family member or friend who helps regularly by doing the necessary tasks so that the sick person can keep as much autonomy as possible. Exclusion Criteria: - aged under 18 - no social coverage - refusal to sign informed consent form

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Hôpital Roger Salengro, CHRU Lille

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary the delay between the diagnosis and the first symptomsIdentification of factors related with diagnosis delay To determine the factors associated with diagnostic delay in young patients (early symptoms before age 60) with Alzheimer's disease or related degenerative disease (Fronto-temporal Lobar Degeneration , Lewy Body Dementia ) 10 years
Secondary Comparison of patient profiles followed at the CMRR-CNR-MAJ Lille and those who are not. The different profiles are defined according to composite measures of socio-demographic type 10 years
Secondary Comparison of patients characteristics followed at the CMRR-CNR-MAJ Lille and those who are not.Impact of the diagnosis on YOD The different characteristics are defined according to composite measures of socio-demographic type 10 years
Secondary the percentage of patients who have had a lack of information about the disease and possible aids Identification of medico-social issues taht have been encountered by YOD patients during the care 10 years
Secondary the percentage of refusal or delay of treatment of certain medico-social aids by the competent authorities Identification of medico-social issues taht have been encountered by YOD patients during the care 10 years
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