FrailtyNCT06988176
Frailty and Muscle Strength Tests in Older Adults Undergoing Major Surgery
An observational study of Frailty and Sarcopenia, run by University of North Carolina, Chapel Hill at 1 site in United States.
Trial summary
The goal of this observational study is to learn if simple tests for frailty and muscle strength can help predict which older adults (age 65 and older) are at higher risk for problems after major abdominal surgery. Read more about this study
- Who is it for?
- Ages 65 years and older
- Conditions the study is for
- Frailty, Sarcopenia, Sarcopenia in Elderly
- What is being tested?
- Frailty assessment, nutrition assessment, cognition assessment, muscle strength testing
- How many people
- 100 participants
- Where
- 1 siteUnited States
- Study dates
- 19 Jun 2025to 4 Aug 2026
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 65 years and older
- All sexes
- No healthy volunteers
- Older adult
Study population: Participants will be older adults (age 65 or older) undergoing planned major abdominal surgeries at the University of North Carolina (UNC) Medical Center. Patients will typically be recruited from the UNC Preoperative Anesthesia Clinic, where standard preoperative assessments are performed.
Who may be able to join
- Participants may be eligible for this study if they meet the following conditions:
- Age 65 years or older.
- Scheduled for elective (planned, non-emergency) 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.
Who cannot join
- Participants will not be eligible for the study if they have any of the following conditions:
- Surgery is an emergency procedure.
- Unable to walk independently (for example, dependent on a wheelchair or bed-bound).
- Significant cognitive impairment that prevents understanding or completing study tests.
Trial locations and contacts
1 site in 1 country.
United States1 site
University of North Carolina
Chapel Hill, North Carolina, 27599
About this study
Official title: Feasibility and Correlation of Functional Muscle Strength Tests and Objective Frailty Measures With Clinical Frailty Scale in Patients Undergoing Major Surgery
The goal of this observational study is to learn if simple tests for frailty and muscle strength can help predict which older adults (age 65 and older) are at higher risk for problems after major abdominal surgery.
The main questions it aims to answer are:
Read more
- Do measures of frailty and muscle strength, taken before surgery, predict complications after surgery?
- Can these tests be easily done during a routine pre-surgical visit?
Participants will:
- Complete brief tests measuring muscle strength, breathing strength, physical function, nutrition status, body composition, and memory during a regular pre-surgical clinic appointment.
- Allow researchers to review their medical records 30 and 90 days after surgery to identify any complications or health problems.
Read the detailed description
This observational study aims to assess whether brief, objective frailty and muscle-strength tests can be feasibly incorporated into routine preoperative evaluations and whether these assessments predict postoperative complications in older adults undergoing elective major abdominal surgery. The broader clinical objective is to enhance perioperative risk stratification using multidimensional frailty measurements.
Study Procedures:
Eligible participants aged 65 years or older scheduled for elective major abdominal surgeries (including colorectal, hepatobiliary, gynecologic, and urologic procedures) will undergo a structured frailty assessment battery during their standard preoperative clinic visit. This battery includes:
- Clinical Frailty Scale (CFS) evaluation
- Maximal Inspiratory Pressure (MIP) and Maximal Expiratory Pressure (MEP) using a MicroRPM handheld respiratory pressure meter
- Hand-grip strength using a Jamar dynamometer
- Timed Up-and-Go (TUG) test
- Skeletal Muscle Index (SMI) measurement via bioimpedance analysis (InBody 120)
- Rectus femoris muscle thickness assessment using portable ultrasound
- Cognitive screening using Mini-Cog test
- Nutritional risk assessment using the Perioperative Nutrition Screen (PONS)
All assessments will be performed by trained clinical research personnel. The entire battery is anticipated to take approximately 20 minutes per participant.
Postoperatively, participant medical records will be reviewed at 30 and 90 days to identify and document complications, ICU admissions, hospital length of stay, discharge disposition, and mortality.
Quality Assurance and Data Validation:
- A comprehensive quality assurance plan includes:
- Routine calibration checks for testing equipment (spirometer, dynamometer, ultrasound, bioimpedance devices).
- Bi-weekly data validation through double data entry and consistency checks in the Research Electronic Data Capture (REDCap) database.
- Source data verification through periodic audits comparing REDCap entries against medical records.
Data Dictionary and Coding:
A detailed data dictionary outlining each variable, units, normal range, and coding schemes is maintained in REDCap. Frailty measures include both raw continuous data and binary categorical flags indicating normal versus abnormal based on established normative values from published consensus guidelines.
Standard Operating Procedures (SOPs):
The following SOPs ensure standardized study execution:
- Patient recruitment and informed consent processes
- Standardized administration of frailty assessments
- Data collection, entry, verification, and management procedures
- Procedures for identification, grading, and reporting postoperative complications
- Regular training and competency evaluation of clinical research personnel
- Procedures for managing protocol deviations and amendments
Sample Size Justification:
The target enrollment of 100 participants provides 80% power to detect moderate correlations (rho ≥0.3) between frailty measures and postoperative complication outcomes, assuming a complication rate of approximately 25%. This sample size also enables adequate power for logistic regression analyses with up to 10 predictors.
Plan for Missing Data:
Missing data will be minimized by rigorous training and immediate data entry verification. In cases where missing data occur, multiple imputation techniques (using chained equations with five iterations) will be employed if ≥5% of values for key predictors or outcomes are missing. Single imputation methods will be avoided except in instances of minimal (<5%) missingness.
Statistical Analysis Plan:
Descriptive statistics will summarize demographic characteristics and frailty test results. Continuous variables will be assessed for normality and summarized appropriately.
For primary analyses:
Logistic regression models will evaluate the predictive capability of frailty measures for postoperative complications.
Model performance metrics will include Area Under the ROC (Receiver Operating Curve), calibration slope and intercept, Brier score, and calibration plots.
For correlations between frailty measures and Clinical Frailty Scale:
Spearman rank correlations and poly-serial correlations will be employed as appropriate for ordinal variables.
All analyses will be conducted using R version 4.3.2 with reproducible seeds set for transparency.
- Conditions
- Frailty, Sarcopenia, Sarcopenia in Elderly, Muscle Strength, Post Operative Complications, Nutrition Assessment
- Being tested
- Frailty assessment, nutrition assessment, cognition assessment, muscle strength testing
- Keywords
- Frailty, sarcopenia, elective abdominal surgery, Muscle strength, Hand Strength, Inspiratory muscle strength, Post operative complications, Risk Assessment, Nutrition Assessment, Elderly patients, Cognitive Function, Physical functional performance
- Medical subject headings
- Frailty, Sarcopenia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Frailty assessment, nutrition assessment, cognition assessment, muscle strength testingDiagnostic test
Participants will undergo a structured frailty and muscle-strength assessment battery performed during their routine preoperative evaluation. These assessments serve as the primary exposure measures of interest and include:
Clinical Frailty Scale (CFS) evaluation (functional frailty assessment) Respiratory muscle strength assessment (Maximal Inspiratory Pressure (MIP) and Maximal Expiratory Pressure (MEP) using a MicroRPM handheld respiratory pressure meter) Hand-grip strength measurement (using Jamar dynamometer) Physical performance evaluation (Timed Up-and-Go (TUG) test) Skeletal muscle mass estimation (Bioelectrical impedance analysis, InBody 120) Muscle thickness measurement (Rectus femoris muscle thickness using portable ultrasound) Cognitive function screening (Mini-Cog test) Nutritional risk screening (Perioperative Nutrition Screen [PONS]) No additional interventions beyond these observational assessments will be conducted.
What is being measured
The primary outcome is the main question the study is designed to answer.
Feasibility of Frailty Assessment Integration
Percentage of participants successfully completing the entire frailty assessment battery within a 20-minute target during routine preoperative visits.
Measured: At the time of the preoperative assessment
Predictive Capability of Frailty Measures for Postoperative Complications
Association between preoperative frailty measures (Clinical Frailty Scale, muscle strength tests, respiratory pressure tests, physical function, cognitive screening, nutritional status, and ultrasound-based muscle thickness) and occurrence of postoperative complications at 30 and 90 days.
Measured: 30 and 90 days postoperatively
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 May 2025
- Study start19 Jun 2025
- Primary completion4 Aug 2026
- Study completion4 Aug 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for FrailtyStudies of the same condition, open and under way.
- More trials run by University of North Carolina, Chapel HillThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 100 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of North Carolina, Chapel Hill
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Monika Nanda, MBBS, MPH, FASA, Principal investigator, University of North Carolina, Chapel Hill
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06988176
- Sponsor's protocol ID
- 25-0481
- Status last verified
- Jan 2026
- First submitted
- 15 May 2025
- Last updated
- 17 Aug 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: De-identified individual participant data (IPD) collected during the study, including frailty measures, complication outcomes, and demographic information, will be made available upon reasonable request.
Study at a glance
From the registry record, last updated by the sponsor on 17 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Feasibility and Correlation of Functional Muscle Strength Tests and Objective Frailty Measures With Clinical Frailty Scale in Patients Undergoing Major Surgery
- ClinicalTrials.gov ID
- NCT06988176
- Acronym / sponsor ID
- 25-0481
- Conditions
- Frailty, Sarcopenia, Sarcopenia in Elderly, Muscle Strength, Post Operative Complications, Nutrition Assessment
- Keywords
- Frailty, sarcopenia, elective abdominal surgery, Muscle strength, Hand Strength, Inspiratory muscle strength, Post operative complications, Risk Assessment
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 100 participants (actual)
- Lead sponsor
- University of North Carolina, Chapel HillUniversity, hospital or other
- Study start
- 19 Jun 2025 (actual)
- Primary completion
- 4 Aug 2026 (actual)
- Study completion
- 4 Aug 2026 (actual)
- First posted
- 23 May 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this observational study is to learn if simple tests for frailty and muscle strength can help predict which older adults (age 65 and older) are at higher risk for problems after major abdominal surgery.
The main questions it aims to answer are:
- Do measures of frailty and muscle strength, taken before surgery, predict complications after surgery?
- Can these tests be easily done during a routine pre-surgical visit?
Participants will:
- Complete brief tests measuring muscle strength, breathing strength, physical function, nutrition status, body composition, and memory during a regular pre-surgical clinic appointment.
- Allow researchers to review their medical records 30 and 90 days after surgery to identify any complications or health problems.
Detailed description
This observational study aims to assess whether brief, objective frailty and muscle-strength tests can be feasibly incorporated into routine preoperative evaluations and whether these assessments predict postoperative complications in older adults undergoing elective major abdominal surgery. The broader clinical objective is to enhance perioperative risk stratification using multidimensional frailty measurements.
Study Procedures:
Eligible participants aged 65 years or older scheduled for elective major abdominal surgeries (including colorectal, hepatobiliary, gynecologic, and urologic procedures) will undergo a structured frailty assessment battery during their standard preoperative clinic visit. This battery includes:
- Clinical Frailty Scale (CFS) evaluation
- Maximal Inspiratory Pressure (MIP) and Maximal Expiratory Pressure (MEP) using a MicroRPM handheld respiratory pressure meter
- Hand-grip strength using a Jamar dynamometer
- Timed Up-and-Go (TUG) test
- Skeletal Muscle Index (SMI) measurement via bioimpedance analysis (InBody 120)
- Rectus femoris muscle thickness assessment using portable ultrasound
- Cognitive screening using Mini-Cog test
- Nutritional risk assessment using the Perioperative Nutrition Screen (PONS)
All assessments will be performed by trained clinical research personnel. The entire battery is anticipated to take approximately 20 minutes per participant.
Postoperatively, participant medical records will be reviewed at 30 and 90 days to identify and document complications, ICU admissions, hospital length of stay, discharge disposition, and mortality.
Quality Assurance and Data Validation:
- A comprehensive quality assurance plan includes:
- Routine calibration checks for testing equipment (spirometer, dynamometer, ultrasound, bioimpedance devices).
- Bi-weekly data validation through double data entry and consistency checks in the Research Electronic Data Capture (REDCap) database.
- Source data verification through periodic audits comparing REDCap entries against medical records.
Data Dictionary and Coding:
A detailed data dictionary outlining each variable, units, normal range, and coding schemes is maintained in REDCap. Frailty measures include both raw continuous data and binary categorical flags indicating normal versus abnormal based on established normative values from published consensus guidelines.
Standard Operating Procedures (SOPs):
The following SOPs ensure standardized study execution:
- Patient recruitment and informed consent processes
- Standardized administration of frailty assessments
- Data collection, entry, verification, and management procedures
- Procedures for identification, grading, and reporting postoperative complications
- Regular training and competency evaluation of clinical research personnel
- Procedures for managing protocol deviations and amendments
Sample Size Justification:
The target enrollment of 100 participants provides 80% power to detect moderate correlations (rho ≥0.3) between frailty measures and postoperative complication outcomes, assuming a complication rate of approximately 25%. This sample size also enables adequate power for logistic regression analyses with up to 10 predictors.
Plan for Missing Data:
Missing data will be minimized by rigorous training and immediate data entry verification. In cases where missing data occur, multiple imputation techniques (using chained equations with five iterations) will be employed if ≥5% of values for key predictors or outcomes are missing. Single imputation methods will be avoided except in instances of minimal (<5%) missingness.
Statistical Analysis Plan:
Descriptive statistics will summarize demographic characteristics and frailty test results. Continuous variables will be assessed for normality and summarized appropriately.
For primary analyses:
Logistic regression models will evaluate the predictive capability of frailty measures for postoperative complications.
Model performance metrics will include Area Under the ROC (Receiver Operating Curve), calibration slope and intercept, Brier score, and calibration plots.
For correlations between frailty measures and Clinical Frailty Scale:
Spearman rank correlations and poly-serial correlations will be employed as appropriate for ordinal variables.
All analyses will be conducted using R version 4.3.2 with reproducible seeds set for transparency.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 65 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Older adult
- Study population
- Participants will be older adults (age 65 or older) undergoing planned major abdominal surgeries at the University of North Carolina (UNC) Medical Center. Patients will typically be recruited from the UNC Preoperative Anesthesia Clinic, where standard preoperative assessments are performed.
Key inclusion criteria (5 listed)
- Age 65 years or older.
- Scheduled for elective (planned, non-emergency) 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.
Key exclusion criteria (4 listed)
- Participants will not be eligible for the study if they have any of the following conditions:
- Surgery is an emergency procedure.
- Unable to walk independently (for example, dependent on a wheelchair or bed-bound).
- Significant cognitive impairment that prevents understanding or completing study tests.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Frailty assessment, nutrition assessment, cognition assessment, muscle strength testingParticipants will undergo a structured frailty and muscle-strength assessment battery performed during their routine preoperative evaluation. These assessments serve as the primary exposure measures of interest and include: Clinical Frailty Scale (CFS) evaluation (functional frailty assessment) Respiratory muscle strength assessment (Maximal Inspiratory Pressure (MIP) and Maximal Expiratory Pressure (MEP) using a MicroRPM handheld respiratory pressure meter) Hand-grip strength measurement (using Jamar dynamometer) Physical performance evaluation (Timed Up-and-Go (TUG) test) Skeletal muscle mass estimation (Bioelectrical impedance analysis, InBody 120) Muscle thickness measurement (Rectus femoris muscle thickness using portable ultrasound) Cognitive function screening (Mini-Cog test) Nutritional risk screening (Perioperative Nutrition Screen [PONS]) No additional interventions beyond these observational assessments will be conducted. | Diagnostic test | – |
Primary outcome
Feasibility of Frailty Assessment Integration
Time frame: At the time of the preoperative assessment
Percentage of participants successfully completing the entire frailty assessment battery within a 20-minute target during routine preoperative visits.
Predictive Capability of Frailty Measures for Postoperative Complications
Time frame: 30 and 90 days postoperatively
Association between preoperative frailty measures (Clinical Frailty Scale, muscle strength tests, respiratory pressure tests, physical function, cognitive screening, nutritional status, and ultrasound-based muscle thickness) and occurrence of postoperative complications at 30 and 90 days.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Aug 2026.
- Individual participant dataSharing planned: Yes. De-identified individual participant data (IPD) collected during the study, including frailty measures, complication outcomes, and demographic information, will be made available upon reasonable request.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Monika Nanda, MBBS, MPH, FASA principal investigator
University of North Carolina, Chapel Hill
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Frailty and Sarcopenia, run by University of North Carolina, Chapel Hill at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 17 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Feasibility of Frailty Assessment Integration (time frame: At the time of the preoperative assessment). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Aug 2026.