Palliative and End-of-life Care in Advanced Dementia: Evaluation of a Program of Organization of Care in Long-term Care
1 other identifier
observational
175
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Sep 2012
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 7, 2011
CompletedFirst Posted
Study publicly available on registry
September 28, 2011
CompletedStudy Start
First participant enrolled
September 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2014
CompletedMarch 31, 2015
March 1, 2015
2.1 years
September 7, 2011
March 30, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
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
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
Study Arms (2)
Training of staff
No training of staff
Eligibility Criteria
Residents in long term care settings
You may qualify if:
- Residents with advanced dementia with a score of 7 on the Reisberg scale
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Laval Universitylead
Study Sites (1)
Centre de santé et de services sociaux de la Vieille Capitale
Québec, Quebec, G1S 2A4, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professeur titulaire
Study Record Dates
First Submitted
September 7, 2011
First Posted
September 28, 2011
Study Start
September 1, 2012
Primary Completion
October 1, 2014
Study Completion
October 1, 2014
Last Updated
March 31, 2015
Record last verified: 2015-03