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Patients With Alzheimer's Disease or Related Youth Disease

Patients With Alzheimer's Disease or Related Youth Disease

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03508024
Acronym
PARMAAJJ
Enrollment
220
Registered
2018-04-25
Start date
2018-01-05
Completion date
2019-04-25
Last updated
2021-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer Disease, Early Onset, Frontotemporal Lobar Degeneration, Lewy Body Disease

Brief 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.

Interventions

None listed

Sponsors

University Hospital, Lille
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
the delay between the diagnosis and the first symptomsIdentification of factors related with diagnosis delay10 yearsTo 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 )

Secondary

MeasureTime frameDescription
Comparison of patient profiles followed at the CMRR-CNR-MAJ Lille and those who are not.10 yearsThe different profiles are defined according to composite measures of socio-demographic type
Comparison of patients characteristics followed at the CMRR-CNR-MAJ Lille and those who are not.Impact of the diagnosis on YOD10 yearsThe different characteristics are defined according to composite measures of socio-demographic type
the percentage of patients who have had a lack of information about the disease and possible aids10 yearsIdentification of medico-social issues taht have been encountered by YOD patients during the care
the percentage of refusal or delay of treatment of certain medico-social aids by the competent authorities10 yearsIdentification of medico-social issues taht have been encountered by YOD patients during the care

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026