Skip to main content
Clinical Trials/NCT00824967
NCT00824967
Terminated
Not Applicable

Not Pharmacologic Treatment Has Illness of Alzheimer and Pathologies Related. Application in Disturbances of Behaviour in EHPAD

Centre Hospitalier Universitaire de Nice1 site in 1 country306 target enrollmentOctober 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
ALZHEIMER Disease
Sponsor
Centre Hospitalier Universitaire de Nice
Enrollment
306
Locations
1
Primary Endpoint
Changes at the behavioural assessment (CMAI, OS, NPI) after 8 weeks of intervention
Status
Terminated
Last Updated
14 years ago

Overview

Brief Summary

Background: Behavioural and psychological symptoms of dementia (BPSD) are often reported in institutions for the elderly.

Objective: To evaluate the effectiveness of a staff education intervention to manage BPSD in older people with a diagnosis of dementia.

Detailed Description

Background: Behavioural and psychological symptoms of dementia (BPSD) are often reported in institutions for the elderly. Objective: To evaluate the effectiveness of a staff education intervention to manage BPSD in older people with a diagnosis of dementia. Methods: The trial was conducted in 16 nursing homes; 306 patients with a diagnosis of dementia and presenting BPSD were selected. Nursing homes were randomly allocated to an intervention group or a control group. An eight-week staff education and training programme was conducted in the nursing homes in the intervention group. The main outcome measures were the Cohen-Mansfield Agitation Inventory (CMAI) and an observation scale score. Assessments were done at baseline (W0), at the end of the 'intervention' period (W8) and 12 weeks after (W20).

Registry
clinicaltrials.gov
Start Date
October 2007
End Date
October 2009
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Alzheimer disease

Exclusion Criteria

  • Not alzheimer disease

Outcomes

Primary Outcomes

Changes at the behavioural assessment (CMAI, OS, NPI) after 8 weeks of intervention

Time Frame: 8 weeks after intervention

Secondary Outcomes

  • Changes at the behavioural assessment (CMAI, OS, NPI) 16 weeks after the end of the intervention(16 weeks after intervention)

Study Sites (1)

Loading locations...

Similar Trials