The PACO Study ("Personnalité Alzheimer COmportement")

NCT ID: NCT01297140

Last Updated: 2014-10-03

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 252 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-01-31
• Study Completion Date: 2015-11-30

Brief Summary

Alzheimer's disease is characterised by a loss of cognitive functions and behavioural problems as set out under the term "Behavioural and psychological symptoms of dementia (BPSD)". The impact of BPSD in everyday life has heavy consequences for the patient and their family. The precocity of incidence, the frequency and the intensity of the BPSD are associated with a rapid decline in cognitive functions, an alteration in the activities of daily living, and a decrease in the quality of life for both the patient and the helper, an increased risk of hospitalisation and of institutionalisation as well as an increase in the cost to the health system. A greater understanding of the risk factors for the occurence of the BPSD would better allow the detection of patients who are particularly at risk for BPSD, to anticipate the crisis situations by proposing early and adapted care, and to better target the medicinal therapies. Certain observational arguments or results of retrospective studies speak in favour of the role of the basic personality in the occurence of BPSD in Alzheimer's disease. The investigators propose to clarify this role through a prospective study.

Conditions

Alzheimer Disease

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Blinding Strategy: NONE

Study Groups

questionary

Group Type: EXPERIMENTAL

questioning

Intervention Type: BEHAVIORAL

Patients will be screened by questioning them and their caregiver and from the results of the clinical examination and the biological and neuroradiological tests habitually carried out in cases of dementia and following accepted procedures.

Interventions

questioning

Patients will be screened by questioning them and their caregiver and from the results of the clinical examination and the biological and neuroradiological tests habitually carried out in cases of dementia and following accepted procedures.

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Male or female subject aged over 50 years ;
• In-patient or out-patient at one of the centres participating in the study ;
• Meeting all the diagnostic criteria for dementia due to AD (NINCDS ADRDA, CDR 1 or 2) or pre-dementia with a CDR of 0.5 (Berr et al., 2006, Dubois et al, 2007) ;
• Covered by the state's Social Security system ;
• With sufficient visual, auditory and oral and written French language skills to complete the clinical and neuropsychological evaluations ;
• Accompanied by a caregiver in sufficient contact with the subject to be able to assess their personality and note the onset of changes in behaviour.

Exclusion Criteria

• Patients with a progressive and/or poorly managed psychiatric pathology (patients with stabilised depression could be included in the study) ;
• Patients taking any neuroleptic psychotropic medication ;
• Patients taking other psychotropic medication, with the exception of any antidepressant, hypnotic, anxiolytic, acetylcholinesterase inhibitors or Memantine which has been prescribed and stabilised for more than 3 months
• Patients with forms of dementia with an aetiology other than that of Alzheimer's disease (frontotemporal dementia, vascular dementia, Lewy Body dementia, and types of dementia that arise as a result of an underlying untreated disease, such as dysthyroidism, vitamin B12 or folic acid deficiency, syphilis, anaemia or hydroelectrolytic disorders) ;
• Patients with serious, progressive or unstable pathologies which could interfere with the variables under consideration ;
• Deafness or blindness which could compromise evaluation of the patient ;
• Pregnancy ;
• Patients under any type of guardianship or belonging to a restricted category as laid out in the Public Health Code ;
• Patients without a suitable caregiver willing to participate.

• Minimum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Hospices Civils de Lyon

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Service de Gériatrie - Hôpital des Charpennes - Hospices Civils de Lyon

Villeurbanne, , France

Site Status: RECRUITING

Countries

France

Central Contacts

Pierre KROLAK-SALMON, Professor

Role: CONTACT

pierre.krolak-salmon@chu-lyon.fr

04.72.43.31.13

Facility Contacts

Pierre KROLAK-SALMON, Professor

Role: primary

pierre.krolak-salmon@chu-lyon.fr

04.72.43.31.13

References

Rouch I, Dorey JM, Boublay N, Henaff MA, Dibie-Racoupeau F, Makaroff Z, Harston S, Benoit M, Barrellon MO, Federico D, Laurent B, Padovan C, Krolak-Salmon P; PACO group. Personality, Alzheimer's disease and behavioural and cognitive symptoms of dementia: the PACO prospective cohort study protocol. BMC Geriatr. 2014 Oct 10;14:110. doi: 10.1186/1471-2318-14-110.

Reference Type: DERIVED

PMID: 25304446 (View on PubMed)

Other Identifiers

2008.508

Identifier Type: -

Identifier Source: org_study_id