Realities, Expectations and Attitudes to Life Support Technologies in Intensive Care for Octogenarians: (Realistic 80)
This study has been completed.
Sponsor:
Daren K. Heyland
Collaborator:
Canadian Institutes of Health Research (CIHR)
Information provided by (Responsible Party):
Daren K. Heyland, Clinical Evaluation Research Unit at Kingston General Hospital
ClinicalTrials.gov Identifier:
NCT01293708
First received: February 10, 2011
Last updated: February 19, 2013
Last verified: February 2013
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Purpose
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.
| Condition |
|---|
|
Critically Ill |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Realities, Expectations and Attitudes to Life Support Technologies in Intensive Care for Octogenarians: |
Further study details as provided by Clinical Evaluation Research Unit at Kingston General Hospital:
Primary Outcome Measures:
- Health Related Quality of Life (HRQOL) [ Time Frame: 12 months ] [ Designated as safety issue: No ]To determine the 12 month HRQOL of 80+ year olds admitted to the ICU in Canada.
Secondary Outcome Measures:
- To determine which patient characteristics are associated with 12-month HRQOL [ Time Frame: 12 month ] [ Designated as safety issue: No ]
- To determine which patient characteristics are associated with functional status. [ Time Frame: 12 months ] [ Designated as safety issue: No ]
- To determine which patient characteristics are associated with survival [ Time Frame: 12 months ] [ Designated as safety issue: No ]
| Enrollment: | 610 |
| Study Start Date: | September 2009 |
| Study Completion Date: | February 2013 |
| Primary Completion Date: | February 2011 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
|
80+ year olds
All 80+ year old that had had an ICU stay of >=24 hrs.
|
Show Detailed Description Eligibility| Ages Eligible for Study: | 80 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
80+ year old admitted to ICU
Criteria
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
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01293708
Locations
| Canada, Alberta | |
| Foothills Hospital | |
| Calgary, Alberta, Canada, T2N 2T9 | |
| University of Alberta Hospital | |
| Calgary, Alberta, Canada, T6G 2B7 | |
| Peter Lougheed Hospital | |
| Calgary, Alberta, Canada, T1Y 6J4 | |
| Royal Alexandra Hospital | |
| Edmonton, Alberta, Canada, T5H 1A8 | |
| Grey Nuns Community Hospital | |
| Edmonton, Alberta, Canada, T6T 0Z0 | |
| Canada, British Columbia | |
| Royal Columbian Hospital | |
| New Westminster, British Columbia, Canada, V3L 3W4 | |
| Surrey Memorial Hospital | |
| Surrey, British Columbia, Canada, V3W | |
| Royal Jubilee Hospital | |
| Vancouver, British Columbia, Canada, V8R 1J8 | |
| Victoria General Hospital | |
| Vancouver, British Columbia, Canada, V8Z 6R5 | |
| St.Paul's Hospital | |
| Vancouver, British Columbia, Canada, V6Z 1Y6 | |
| Canada, Manitoba | |
| Winnipeg Health Sciences Center | |
| Winnipeg, Manitoba, Canada, R3A 1R9 | |
| St. Boniface Hospital | |
| Winnipeg, Manitoba, Canada, R2H 2A6 | |
| Canada, Ontario | |
| St. Joseph's Healthcare | |
| Hamilton, Ontario, Canada, L8N 4A6 | |
| Kingston General Hospital | |
| Kingston, Ontario, Canada, K7L 2V7 | |
| Ottawa Hospital | |
| Ottawa, Ontario, Canada, K1Y 4E9 | |
| Mount Sinai | |
| Toronto, Ontario, Canada, M5G 1X5 | |
| Sunnybrook Health Sciences | |
| Toronto, Ontario, Canada, M4N 3M5 | |
| Toronto General Hospital | |
| Toronto, Ontario, Canada, M5G 2C4 | |
| St. Michaels Hospital | |
| Toronto, Ontario, Canada, M5B 1W8 | |
| Canada, Quebec | |
| Hospital Maisonneuve-Rosemont | |
| Montreal, Quebec, Canada, H1T 2M4 | |
| Hospital de Sacre-Coeur | |
| Montreal, Quebec, Canada, H4J 1C5 | |
| Canada, Saskatchewan | |
| Royal University Hospital | |
| Saskatoon, Saskatchewan, Canada, S7N 0W8 | |
| Canada | |
| Departement d'Anesthesie | |
| Quebec, Canada, G1J 1Z4 | |
| Hospital Laval | |
| Quebec, Canada, G1V 4G5 | |
Sponsors and Collaborators
Daren K. Heyland
Canadian Institutes of Health Research (CIHR)
Investigators
| Study Chair: | Daren Heyland, MD | Clinical Evaluation Research Unit,, Kingston General Hospital |
More Information
No publications provided
| Responsible Party: | Daren K. Heyland, Dr. Daren Heyland, Clinical Evaluation Research Unit at Kingston General Hospital |
| ClinicalTrials.gov Identifier: | NCT01293708 History of Changes |
| Other Study ID Numbers: | R80 |
| Study First Received: | February 10, 2011 |
| Last Updated: | February 19, 2013 |
| Health Authority: | Canada: Queen's University Health Sciences and Affliated Teaching Hospitals Research Ethics |
Keywords provided by Clinical Evaluation Research Unit at Kingston General Hospital:
|
Octogenarians HRQOL mortality prospective observational Elderly |
Additional relevant MeSH terms:
|
Critical Illness Disease Attributes Pathologic Processes |
ClinicalTrials.gov processed this record on May 23, 2013