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Clinical Trials/NCT02351453
NCT02351453
Completed
Not Applicable

Patients With Alzheimer Disease, Spouse Carers and Risk of Institutionalization: a Prospective Observational Cohort Study of Dyads (AID Study)

University Hospital, Angers1 site in 1 country207 target enrollmentAugust 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Alzheimer Disease
Sponsor
University Hospital, Angers
Enrollment
207
Locations
1
Primary Endpoint
Date of institutionalization of AD patients (standardized questionnaire)
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The primary objective of AID study is to identify the medico-neuropsychological, socio-economic and environmental baseline characteristics of dyads associated with the institutionalization of AD patients.

Detailed Description

In order to reduce Alzheimer Disease (AD) adverse impacts at individual level as well as in terms of expenditures, the development of efficient strategies based on the identification and the correction of risk factors of institutionalization of AD patients proves necessary. While it has been identified that institutionalization date depends on patients' health characteristics, the role of social, economic and environmental factors still remains few known. The investigators hypothesized that institutionalization of AD patients could be related not only to medico-neuropsychological patients' characteristics but also to socio-economic and environmental characteristics of dyad (i.e., AD patient and spouse carer), that could modify the delay of institutionalization.

Registry
clinicaltrials.gov
Start Date
August 2011
End Date
February 2013
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University Hospital, Angers
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Eligibility criteria for AD patients were:
  • Over age 65,
  • Diagnosis of AD according to the NINCDS-ADRDA ( National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer's Disease and Related Disorders Association) criteria,
  • Last memory center consultation between 6 and 12 months before the inclusion,
  • Being affiliated to the French health insurance,
  • Living at home,
  • Having a caregiver with inclusion criteria,
  • Agreement of General Practitioner (GP) of AD patient to participate in the study and affiliation of the GP to the national "Association pour le Développement de l'Information Médicalisée" (ADIM) French network.
  • Eligibility criteria for spouse carers were:
  • Over age 65,

Exclusion Criteria

  • Non inclusion criteria for AD patients and spouse carers were:
  • An inability to understand and speak French,
  • Acute disease in the past month of baseline assessment,
  • Expected moving outside the recruitment area during the follow-up period
  • Concomitant participation in a clinical trial.

Outcomes

Primary Outcomes

Date of institutionalization of AD patients (standardized questionnaire)

Time Frame: This outcome is assessed at 12 months.

Date of entrance in institution was collected by a standardized questionnaire.

Secondary Outcomes

  • The increase formal home help services (measured by a standardized questionnaire and coded as a binary variable)(This outcome is assessed at baseline and 12 months.)
  • The delay of institutionalization of AD patients (assessed by a standardized questionnaire and expressed in number of days)(This outcome is assessed at baseline and 12 months.)

Study Sites (1)

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