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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01293708
Other study ID # R80
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 2009
Est. completion date February 2013

Study information

Verified date December 2020
Source Clinical Evaluation Research Unit at Kingston General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to understand the realities, expectations and attitudes of patients 80+ and their families about the use of life-sustaining technology, and to document the patient outcomes and family experiences associated with surviving and not surviving critical illness. Specifically in this project the investigators will determine the real outcomes of critical illness experienced by octogenarians.


Description:

Seriously ill hospitalized elderly patients rate 'not being kept alive on prolonged life supports' as the most important aspect of good quality care at the end of life (EOL). Across Canada, large numbers of elderly patients near the EOL and their families are faced with decisions about whether or not to use mechanical ventilation or other forms of life support technology used in intensive care units (ICUs). The investigators do not know whether these patients and their families are informed about the realities of intensive care - that is, if they are aware of the likelihood of surviving a critical illness and the resultant health states. The outcomes of critical illness for this patient population and their families are unknown, despite the crucial importance of this information to guide clinical decision making. The goals of our research program are to understand the realities of critical care, and the expectations and attitudes of patients 80 years of age or older (80+) and their families about the use of life sustaining technology. Specifically, in this project, the investigators want to determine the realities or outcomes of surviving critical illness. Our primary research question is: 1. What are the 12-month health-related quality of life (HRQOL), functional status, and survival of patients admitted to ICU who are 80+ years old? Our secondary research questions are: 2. Which patient characteristics are associated with 12-month HRQOL, functional status, and survival? 3. What is the satisfaction of family members with critical care, as measured by the Family Satisfaction in ICU (FS-ICU 24) instrument? 4. For patients surviving their ICU stay, what is the experience of family members caring for the patient during follow up, as measured by the Caregiver Reaction Assessment (CRA) instrument? 5. For patients who do not survive their ICU stay, what is the family satisfaction with EOL care, as measured using the CANHELP Satisfaction (Bereavement) instrument? 6. What is the health-related financial burden experienced by patients and their caregivers during their initial ICU hospitalization and up to 12 months after the index ICU admission? 7. What is the quality of decision making regarding the goals of care for an 80+ ICU patient? 8. What are the values that influence decisions about the goals of care for this population? To answer these questions, the investigators are conducting a national, multicentre, cohort study of 800 patients age 80+ years who are admitted to Canadian ICUs. The investigators will follow these patients prospectively for 12 months to measure study outcomes. In addition, using novel instruments that the investigators have already developed and validated, the investigators will follow family members of these patients to document their experience as caregivers, their satisfaction with care of their relatives, and the financial implications of having a critically ill loved one. This quantitative project will be complemented by a separate qualitative study in the community setting to further understand the expectations and attitudes of persons over 80 years of age regarding the use of life sustaining technology. Data emerging from this work will inform important clinical decisions regarding critical care and EOL care for this aged population. The investigators presume that the short- and long-term mortality of 80+ year olds admitted to Canadian ICUs will be high and that the self-reported health-related quality of life and functional status of survivors after hospital discharge will be low. The investigators anticipate that pre-morbid illnesses and functional status before admission to ICU will correlate with long-term clinical outcomes. The investigators are uncertain as to the psychological and financial burden experienced by families when a loved one is in the ICU and during the recovery phase; our study will be the first to furnish such important information. By using administrative databases to complement information already being collected in this study, the investigators will obtain a better understanding of the healthcare resource utilization and longer term survival of this cohort, and will be better positioned to offer effective ICU and follow-up care for this at-risk patient population.


Recruitment information / eligibility

Status Completed
Enrollment 1504
Est. completion date February 2013
Est. primary completion date February 2013
Accepts healthy volunteers No
Gender All
Age group 80 Years and older
Eligibility Inclusion Criteria: - minimum stay in the ICU of 24 hrs - patient is >=80 years old - patient is a resident of Canada and has a permanent address in this country - patient has an eligible family caregiver who has visited the patient at least once within 96 hours of the current ICU admission Exclusion Criteria: - family caregiver is <= 18 - family caregiver is paid to do so - family caregivers that do not speak English or French - previously enrolled

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Canada Foothills Hospital Calgary Alberta
Canada Peter Lougheed Hospital Calgary Alberta
Canada University of Alberta Hospital Calgary Alberta
Canada Grey Nuns Community Hospital Edmonton Alberta
Canada Royal Alexandra Hospital Edmonton Alberta
Canada St. Joseph's Healthcare Hamilton Ontario
Canada Kingston General Hospital Kingston Ontario
Canada Hospital de Sacre-Coeur Montreal Quebec
Canada Hospital Maisonneuve-Rosemont Montreal Quebec
Canada Royal Columbian Hospital New Westminster British Columbia
Canada Ottawa Hospital Ottawa Ontario
Canada Departement d'Anesthesie Quebec
Canada Hospital Laval Quebec
Canada Royal University Hospital Saskatoon Saskatchewan
Canada Surrey Memorial Hospital Surrey British Columbia
Canada Mount Sinai Toronto Ontario
Canada St. Michaels Hospital Toronto Ontario
Canada Sunnybrook Health Sciences Toronto Ontario
Canada Toronto General Hospital Toronto Ontario
Canada Royal Jubilee Hospital Vancouver British Columbia
Canada St.Paul's Hospital Vancouver British Columbia
Canada Victoria General Hospital Vancouver British Columbia
Canada St. Boniface Hospital Winnipeg Manitoba
Canada Winnipeg Health Sciences Center Winnipeg Manitoba

Sponsors (2)

Lead Sponsor Collaborator
Daren K. Heyland Canadian Institutes of Health Research (CIHR)

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Health Related Quality of Life (HRQOL) To determine the 12 month HRQOL of 80+ year olds admitted to the ICU in Canada. 12 months
Secondary To determine which patient characteristics are associated with 12-month HRQOL 12 month
Secondary To determine which patient characteristics are associated with functional status. 12 months
Secondary To determine which patient characteristics are associated with survival 12 months
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