Performance Evaluation and Research for Older Adults Requiring Major Surgery
PERFORM
1 other identifier
observational
214
1 country
1
Brief Summary
The purpose is to identify modifiable factors in older adults associated with functional decline following major non-emergent surgery. The hypothesis of this proposal is that poor preoperative exercise tolerance and physical performance, potentially modifiable factors, are crucial in predicting functional decline and disability following surgery. When completed, this study will reveal detailed information on the incidence and risk factors for functional decline in older adults following surgery. It will direct future research targeting interventions in older adults at highest risk for functional decline following surgery, thereby decreasing the incidence of premature disability.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2004
Longer than P75 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
Study Start
First participant enrolled
April 1, 2004
CompletedFirst Submitted
Initial submission to the registry
June 15, 2007
CompletedFirst Posted
Study publicly available on registry
June 19, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2008
CompletedStudy Completion
Last participant's last visit for all outcomes
August 31, 2009
CompletedDecember 20, 2022
December 1, 2022
4.8 years
June 15, 2007
December 15, 2022
Conditions
Keywords
Eligibility Criteria
Adults, aged 65 and older, who are undergoing an abdominal or cardiothoracic surgical procedure at the University of Washington Medical Center in Seattle, WA.
You may qualify if:
- years or older;
- Having abdominal surgery;
- Informed consent obtained;
- All races/ethnicities;
- Both genders
You may not qualify if:
- Non-English speaking;
- Unwillingness to participate;
- Unavailable for follow-up phone calls;
- Unable to communicate with researchers;
- Unable to pass the screening test
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Washingtonlead
- National Institutes of Health (NIH)collaborator
Study Sites (1)
University of Washington
Seattle, Washington, 98195, United States
Study Officials
- PRINCIPAL INVESTIGATOR
David R Flum, MD, MPH
University of Washington
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- OTHER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor, Surgery
Study Record Dates
First Submitted
June 15, 2007
First Posted
June 19, 2007
Study Start
April 1, 2004
Primary Completion
December 31, 2008
Study Completion
August 31, 2009
Last Updated
December 20, 2022
Record last verified: 2022-12