- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07365098
Liver Transplant Recipients and 30-Second Lie-to-Sit Test
January 15, 2026 updated by: BÜŞRA CANDİRİ, Inonu University
Assessment of Functional Capacity in Liver Transplant Recipients Using the 30-Second Lie-to-Sit Test
The aim of this study is to assess functional capacity in liver transplant recipients using the 30-second lie-to-sit test and to examine the relationships between functional capacity and variables such as muscle strength, upper and lower extremity function, exercise capacity, and perceived exertion.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
- Other: 30-second lie-to-sit test
- Other: Modified Borg Scale
- Other: waist circumference
- Other: 30-second sit-to-stand test
- Other: Quadriceps muscle strength
- Other: Deltoid muscle strength
- Other: Trunk flexion strength
- Other: Trunk extension strength
- Other: Handgrip strength
- Other: 2-minute walk test
- Other: Upper Extremity Functional Index-15 (UEFI-15)
- Other: Lower Extremity Functional Scale (LEFS)
Detailed Description
Participants' demographic and clinical characteristics, including age, gender, BMI, waist circumference, and relevant clinical data, will be recorded.
Functional capacity will also be assessed using the 30-second sit-to-stand test, the 2-minute walk test, and upper and lower extremity functional scales (UEFI-15, AEFÖ), with perceived exertion measured using the Modified Borg Scale.
Muscle strength will be measured isometrically with a dynamometer for the quadriceps, deltoid, trunk flexor/extensor muscles, and handgrip.
The obtained data will provide a comprehensive evaluation of muscle strength and functional status, contributing to individualized rehabilitation planning.
Study Type
Observational
Enrollment (Estimated)
34
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Büşra CANDİRİ
- Phone Number: +905073780717
- Email: candiri_17@hotmail.com
Study Contact Backup
- Name: İrem Yiğit
- Phone Number: +905375427930
- Email: irem44ahmet@gmail.com
Study Locations
-
-
-
Malatya, Turkey (Türkiye)
- Recruiting
- Inonu Unıversity
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
liver transplant recipients
Description
Inclusion Criteria:
- Adults aged 18-65 years
- Diagnosed with end-stage liver disease and listed for liver transplantation
- Ability to speak, understand, and write in Turkish
- No mental disorders
- Voluntary participation with informed consent
Exclusion Criteria:
- Pulmonary, neurological, or cardiac diseases that may interfere with adherence to the assessment protocol
- Difficulty complying with the assessment program
- Musculoskeletal problems
- History of regular physical activity
- Multiple organ failure
- Cognitive impairment
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
30-second lie-to-sit test
Time Frame: 24 hours
|
In this test, participants will be asked to start from a supine position with their head and arms supported and move to a sitting position as quickly as possible.
They will be allowed to use one hand and, if necessary, a thin cushion to help them sit up.
The number of repetitions performed within 30 seconds will be recorded.
|
24 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Waist Circumference
Time Frame: 24 hours
|
Waist circumference will be measured in centimeters at the narrowest point between the lowest rib and the upper border of the pelvis while the participant is standing, and the value will be recorded.
|
24 hours
|
|
Modified Borg Scale
Time Frame: 24 hours
|
Following the 30-second lie-to-sit test, the modified Borg scale will be used to assess participants' perceived exertion levels.This scale is a standard tool that allows individuals to subjectively assess their level of exertion during physical activity or exercise, rated from 0 (no exertion) to 10 (maximum exertion).
|
24 hours
|
|
30-second sit-to-stand test
Time Frame: 24 hours
|
The 30-second sit-to-stand test will be used to assess participants' lower extremity muscle strength and functional capacity.
In this test, the participant sits with their back against a chair, feet flat on the floor, and arms crossed over the chest, and stands up and sits down as many times as possible within 30 seconds.
Hands should not touch the chair during the test, and only full, complete repetitions are counted.
The total number of repetitions at the end of the test will be recorded.
|
24 hours
|
|
Quadriceps muscle strength
Time Frame: 24 hours
|
Quadriceps muscle strength will be measured isometrically using a hand-held dynamometer.
The participant will be seated with the knees flexed at 90°.
The dynamometer will be placed on the front of the leg at ankle level, and the participant will be asked to lift the leg with maximal effort.
Three measurements will be taken for each leg, and the average value will be recorded.
|
24 hours
|
|
Deltoid muscle strength
Time Frame: 24 hours
|
Isometric strength of the deltoid muscle will be assessed using a hand-held dynamometer.
The participant will be seated with the shoulder positioned at 90° abduction and the elbow slightly flexed.
The dynamometer will be placed on the lateral side of the upper arm at elbow level, and the participant will perform maximum-effort shoulder abduction.
Three measurements will be taken for each extremity, and the average value will be recorded.
|
24 hours
|
|
Trunk flexion strength
Time Frame: 24 hours
|
The isometric trunk flexion strength test will be performed with the participant positioned supine, with the knees extented or the hips flexed at 30°.
The dynamometer will be placed below the suprasternal notch of the sternum.
The participant will place their hands on the opposite acromions and perform isometric trunk flexion.
|
24 hours
|
|
Trunk extension strength
Time Frame: 24 hours
|
The isometric trunk extension strength, the participant will be positioned prone while lying down.
The dynamometer will be placed at the T4 level, and the participant will be asked to perform maximum isometric trunk extension.
In each test position, participants will first perform a submaximal trial, followed by three correct repetitions, and the average value will be recorded.
|
24 hours
|
|
Handgrip strength
Time Frame: 24 hours
|
Handgrip strength will be assessed using a hand dynamometer.
Participants will be seated with their shoulders adducted at the sides, elbows flexed at 90°, forearms in a neutral position, and wrists positioned at 0-30° extension and 0-15° ulnar deviation.
Three trials will be performed for each hand, with a 30-second rest between trials.
For analysis, the average of three measurements for both hands will be recorded.
|
24 hours
|
|
2-minute Walk Test
Time Frame: 24 hours
|
The 2-minute walk test will be used to assess participants' exercise capacity and physical performance.
During the test, participants will walk at a self-selected, safe pace for two minutes, and the distance covered in meters will be recorded.
|
24 hours
|
|
Upper Extremity Functional Index-15 (UEFI-15)
Time Frame: 24 hours
|
This questionnaire consists of 15 items that assess difficulties in using the upper extremities for activities of daily living.
Each item is scored from 0 (cannot do) to 4 (no difficulty).
The raw score ranges from 0 to 59 and is converted to a final score ranging from 0 to 100.
A higher final score indicates better upper extremity function, providing a comprehensive assessment of functional capacity.
|
24 hours
|
|
Lower Extremity Functional Scale (LEFS)
Time Frame: 24 hours
|
This questionnaire is important for assessing lower extremity functional capacity and examining activity limitations in various lower extremity disorders.
It consists of 20 items, each scored from 0 (extreme difficulty or unable to perform the activity) to 4 (no difficulty).
Intermediate values are defined as 1 (quite difficult), 2 (moderately difficult), and 3 (somewhat difficult).
The total score ranges from 0 to 80, with higher scores indicating better functional level.
|
24 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 8, 2025
Primary Completion (Estimated)
October 20, 2026
Study Completion (Estimated)
December 20, 2026
Study Registration Dates
First Submitted
January 15, 2026
First Submitted That Met QC Criteria
January 15, 2026
First Posted (Actual)
January 26, 2026
Study Record Updates
Last Update Posted (Actual)
January 26, 2026
Last Update Submitted That Met QC Criteria
January 15, 2026
Last Verified
November 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025/8550
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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