Actively Recruiting

Age: 65Years +
All Genders
ID06988176

Feasibility and Correlation of Functional Muscle Strength Tests and Objective Frailty Measures With Clinical Frailty Scale in Patients Undergoing Major Surgery

Led by University of North Carolina, Chapel Hill · Updated on 2026-01-28

100

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying whether simple tests for frailty and muscle strength can help predict which adults aged 65 and older face higher risks of problems after major abdominal surgery. This observational study aims to see if these quick assessments can be easily included in routine pre-surgical visits and if they can effectively predict postoperative complications. The goal is to improve how risks are assessed before surgery using various measures of frailty. Participants will undergo a series of brief tests during their usual preoperative clinic visit. These tests include evaluating frailty with the Clinical Frailty Scale, measuring respiratory muscle strength with handheld devices, assessing hand-grip strength, performing the Timed Up-and-Go test, estimating skeletal muscle mass via bioelectrical impedance, measuring muscle thickness using ultrasound, screening cognitive function with the Mini-Cog test, and assessing nutritional risk using the Perioperative Nutrition Screen. All tests are performed by trained staff and take about 20 minutes. After surgery, researchers will review participants' medical records at 30 and 90 days to identify any complications or health issues. During the study, participants complete these physical and cognitive assessments only once during their pre-surgical visit. Researchers collect and validate data carefully with quality assurance plans including equipment calibration and data checks. The main measures include how feasible it is to add these tests into routine care and how well the frailty assessments predict complications after surgery. Participants are observed through medical records for up to 90 days after surgery to monitor outcomes. The study is expected to enroll about 100 participants and continues through August 2026.

CONDITIONS

Brief Title

Frailty and Muscle Strength Tests in Older Adults Undergoing Major Surgery

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 65 years or older
  • Scheduled for elective major abdominal surgery including colorectal, hepatobiliary, gynecologic, or urologic procedures
  • Able to attend a routine preoperative evaluation visit
  • Able and willing to complete brief assessments for muscle strength, walking, breathing strength, memory, and nutrition
Not Eligible

You will not qualify if you...

  • Emergency surgery
  • Unable to walk independently (for example, dependent on a wheelchair or bed-bound)
  • Significant cognitive impairment that prevents understanding or completing study tests

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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)

Diagnostic Evaluation

Duration - At the time of the preoperative assessment

Participants undergo a structured frailty and muscle-strength assessment battery during their routine preoperative evaluation. This includes assessments of functional frailty, respiratory muscle strength, hand-grip strength, physical performance, skeletal muscle mass, muscle thickness, cognitive function, and nutritional risk.

1 visit (in-person)

Long-term Monitoring

Duration - 90 days postoperatively

Participants' medical records are reviewed postoperatively at 30 and 90 days to identify and document complications, ICU admissions, hospital length of stay, discharge disposition, and mortality.

2 medical record reviews (no in-person visits)

Trial Site Locations

Total: 1 location

1

University of North Carolina

Chapel Hill, North Carolina, United States, 27599

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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