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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01441726
Other study ID # MOP-114881
Secondary ID
Status Completed
Phase N/A
First received September 7, 2011
Last updated March 30, 2015
Start date September 2012
Est. completion date October 2014

Study information

Verified date March 2015
Source Laval University
Contact n/a
Is FDA regulated No
Health authority Canada: Canadian Institutes of Health Research
Study type Observational

Clinical Trial Summary

Rationale: In Canada, as in most industrialized countries, Alzheimer's disease and other related dementia are increasingly prevalent in older people. At an advanced stage, institutionalization in a long-term care (LTC) setting will be the fate of a majority of patients. A structured palliative care approach is increasingly used for cancer patients, but is still rarely accessible in LTC institutions for older people with advanced or terminal dementia. This approach should include a more systematic detection and treatment of pain and other physical and psychological symptoms during the last weeks of life, as well as better communications between patients, families and care staff, particularly relating to advanced care directives. Objectives: The general objective of this study is to implement and evaluate a multidisciplinary and multidimensional program of palliative and end-of-life care for older persons with terminal dementia in LTC facilities. Methodology: The intervention program will include five components:

1. daily involvement of a nurse from the regular staff in the LTC facility as a change agent;

2. awareness sessions with administrators and staff on the importance of high quality palliative care in dementia;

3. a training program for physicians and all the staff involved in direct care of patients;

4. systematic discussions with families and distribution to families of a document on different aspects of palliative care in dementia;

5. systematic clinical care by regular staff for the control of pain, respiratory symptoms and mouth care. The program will be implemented in two LTC settings (one in Quebec City and one in Sherbrooke, Quebec, Canada), and results will be compared with the LTC control settings where usual care will be applied without implementation of the program.


Recruitment information / eligibility

Status Completed
Enrollment 175
Est. completion date October 2014
Est. primary completion date October 2014
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

Residents with advanced dementia with a score of 7 on the Reisberg scale

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Canada Centre de santé et de services sociaux de la Vieille Capitale Quebec City Quebec

Sponsors (1)

Lead Sponsor Collaborator
Laval University

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Family satisfaction with terminal care Family Perception of Care Scale (FPCS): 25-item validated instrument including 4 components, yielding a score from 25 (negative perception) to 175 (highest positive perception of quality of palliative care) 1 year No
Primary Comfort scale in last two weeks of life Comfort Assessment in Dying with Dementia (CAD-EOL): 14-item validated instrument including 4 sub-scales, yielding a score from 14 (low comfort level) to 42 (highest comfort level). 2 weeks No
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