Actively Recruiting

Age: 70Years +
All Genders
Healthy Volunteers
ID07367828

Feasibility and Validity of Frailty Screening Tools as a Measure of Postoperative Outcomes in Older Patients Undergoing Elective Surgery

Led by University of Iceland · Updated on 2026-01-26

350

Participants Needed

1

Research Sites

29 weeks

Total Duration

On this page

Sponsors

U

University of Iceland

Lead Sponsor

L

Landspitali University Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Frailty is a common condition in older adults characterized by reduced physical reserve and increased vulnerability to stress, which can lead to complications after surgery such as longer hospital stays, readmissions, and higher mortality. This research aims to evaluate and validate three frailty screening tools—PRISMA-7 questionnaire, Timed Up & Go (TUG) test, and Clock Drawing Test (CDT)—to identify elderly patients at risk for complications before elective surgery. The study seeks to better understand frailty's impact on postoperative outcomes and find an efficient screening method suitable for large elderly populations. The study will include patients aged 70 and older who are scheduled for intermediate or major elective surgery at a hospital in Iceland. Frailty will be assessed using the PRISMA-7 questionnaire, the TUG test, and the CDT. Patients scoring positive on the CDT (2 or fewer out of 3 points) and TUG (taking 11 seconds or more) will be classified as frail, while others will serve as controls. Clinical data and postoperative outcomes including complications, readmission within 90 days, delirium, length of hospital stay, discharge status, and mortality up to 1 year will be collected from medical records. Participants will be screened during their preoperative assessment at the anesthesia outpatient clinic. Researchers will measure surgical complications up to 30 days after surgery and monitor readmissions for 90 days. They will also track length of hospital stay, delirium occurrence, discharge destination, and mortality for up to 180 days or 1 year after surgery. The study offers a comprehensive look at how frailty screening may predict risks and improve care for older surgical patients.

CONDITIONS

Brief Title

Validity of Frailty Screening Tools as a Measure for Postoperative Outcomes

Who Can Participate

Age: 70Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 70 years or older who present for preoperative work-up at the anesthesia department
  • Patients scheduled to undergo intermediate or major elective surgery
Not Eligible

You will not qualify if you...

  • Not undergoing planned surgery

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) at the anesthesia outpatient clinic for preoperative assessment including frailty screening tests

Surgery

Duration - Day of surgery

Participants undergo intermediate or major elective surgery at the hospital.

1 hospital visit for surgery

Post-operative Follow-up

Duration - Up to 1 year after surgery

Participants are monitored for surgical complications, length of hospital stay, delirium, discharge disposition, readmission, and mortality.

Hospital stay and follow-up assessments up to 180 days postoperatively with monitoring for readmission up to 90 days and mortality up to 1 year

Trial Site Locations

Total: 1 location

1

Landspitali - The national university hospital in Iceland.

Reykjavik, Hofudborgarsvaedid, Iceland, 101

Actively Recruiting

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Research Team

M

Martin I Sigurdsson, MD, PhD

L

Luis G Rabelo, B.Sc

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

Frailty assessment tools and associated postoperative outcomes in older patients undergoing elective surgery: A prospective pilot study.

Luis G Rabelo, Anna Bjornsdottir, Anna B Jonsdottir...

https://pubmed.ncbi.nlm.nih.gov/36307919