- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03160222
Validation of Bedside Ultrasound to Predict Body Composition in Non- and Critically Ill Patients (USVALID)
August 28, 2019 updated by: Arabella Fischer, MD, Medical University of Vienna
Validation of Bedside Ultrasound to Predict Body Composition in Non- and Critically Ill Patients: The USVALID Prospective Study
The prospective study will include 200 patients and 50 critically ill patients, who had an abdominal computed tomography (CT) scan including the L3 level for any clinical reason.
Ultrasound scans of the anterior thighs and forearms will be taken after the CT scan within 48 hours.
Bioelectrical impedance analysis (BIA) will also be performed.
In addition muscle strength, mobility, physical function and nutrition will be assessed.
Primary outcome is the prediction of CT-based whole body muscle and fat volume and BIA-based fat and lean body mass from ultrasound-based muscle and fat thickness.
Other secondary outcomes include the intra- and interrater reliability of the CT evaluation and ultrasound examination of muscle and fat mass.
The relationship between clinical aspects (strength, mobility, physical function, nutrition) and whole body composition is another secondary outcome.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
250
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Vienna, Austria, 1180
- Medical University of Vienna
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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
14 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- cross-sectional abdominal CT scan including the level of L3 vertebra for any clinical reason
- study-related ultrasound examination must take place within 48 hours of CT
Exclusion Criteria:
- patients younger than 18 years
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
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Body Composition Measurements
Body composition measurements comprise the ultrasound measurement of fat and muscle thickness of both upper arms and thighs, the bioelectrical impedance analysis (BIA), measurement of weight, handgrip strength, overall muscle strength (Medical Research Council scale) and questionnaires about physical activity, nutrition and fluid status.
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Body composition measurements comprise the ultrasound measurement of fat and muscle thickness of both upper arms and thighs, the bioelectrical impedance analysis (BIA), measurement of weight, handgrip strength, overall muscle strength (Medical Research Council scale) and questionnaires about physical activity, nutrition and fluid status.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
prediction (r2) of CT-based whole body muscle volume from ultrasound-based muscle thickness
Time Frame: Ultrasound measurement once-only within 48 hours after the CT scan
|
In a linear regression model, the dependent variable is CT-based whole body muscle volume.
The independent variable is ultrasound-based muscle thickness.
The prediction (r2) of CT-based muscle volume in the multiple linear regression model is the outcome.
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Ultrasound measurement once-only within 48 hours after the CT scan
|
|
prediction (r2) of CT-based whole body fat volume from ultrasound-based fat thickness
Time Frame: Ultrasound measurement once-only within 48 hours after the CT scan
|
In a linear regression model, the dependent variable is CT-based whole body fat volume.
The independent variable is ultrasound-based fat thickness.
The prediction (r2) of CT-based fat volume in the multiple linear regression model is the outcome.
|
Ultrasound measurement once-only within 48 hours after the CT scan
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
prediction (r2) of BIA-based whole body muscle volume from ultrasound-based muscle thickness
Time Frame: BIA measurement once-only within 48 hours after the CT scan
|
In a linear regression model, the dependent variable is BIA-based whole body muscle volume.
The independent variable is ultrasound-based muscle thickness.
The prediction (r2) of BIA-based muscle volume in the multiple linear regression model is the outcome.
|
BIA measurement once-only within 48 hours after the CT scan
|
|
prediction (r2) of BIA-based whole body fat volume from ultrasound-based fat thickness
Time Frame: BIA measurement once-only within 48 hours after the CT scan
|
In a linear regression model, the dependent variable is BIA-based whole body fat volume.
The independent variable is ultrasound-based fat thickness.
The prediction (r2) of BIA-based fat volume in the multiple linear regression model is the outcome.
|
BIA measurement once-only within 48 hours after the CT scan
|
|
intrarater reliability (bias in Bland Altman analysis) of ultrasound muscle/fat thickness
Time Frame: repeated US measurement in 60 patients once-only within 48 hours after the CT scan
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For intrarater reliability each of the 5 examiners repeats the ultrasound measurement in 12 patients.
In a Bland Altman analysis, the mean difference (=bias) in muscle/fat thickness between repeated measurements of the same examiner is the outcome.
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repeated US measurement in 60 patients once-only within 48 hours after the CT scan
|
|
interrater reliability (bias in Bland Altman analysis) of ultrasound muscle/fat thickness
Time Frame: repeated US measurement in 60 patients once-only within 48 hours after the CT scan
|
For interrater reliability each of the 10 different pairs of examiners analyzes 6 patients.
For each pair both examiners perform the ultrasound examination.
In a Bland Altman analysis, the mean difference (=bias) in ultrasound muscle/fat thickness between examiners is the outcome.
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repeated US measurement in 60 patients once-only within 48 hours after the CT scan
|
|
muscle strength in patients with different CT-based body compositions (sarcopenia, malnutrition, obesity, sarcopenic obesity)
Time Frame: muscle strength measurement once-only within 48 hours after the CT scan
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Muscle strength is measured with MRC scale and hand dynamometry.
The outcome is muscle strength evaluated in different patient's group according to their CT-based body composition.
Sarcopenia is defined as lowered L3 skeletal muscle index.
Malnutrition is defined at a BMI beneath18,5 kg/m².
Obesity is defined as a BMI above or equal to 30 kg/m².
Sarcopenia obesity is defined as lowered L3 skeletal muscle indices and a BMI above or equal to 30 kg/m2.
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muscle strength measurement once-only within 48 hours after the CT scan
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Arabella Fischer, Dr., Medical University of Vienna
- Study Director: Michael Hiesmayr, Prof. Dr., Medical University of Vienna
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Weijs PJ, Looijaard WG, Dekker IM, Stapel SN, Girbes AR, Oudemans-van Straaten HM, Beishuizen A. Low skeletal muscle area is a risk factor for mortality in mechanically ventilated critically ill patients. Crit Care. 2014 Jan 13;18(2):R12. doi: 10.1186/cc13189.
- Takai Y, Ohta M, Akagi R, Kato E, Wakahara T, Kawakami Y, Fukunaga T, Kanehisa H. Applicability of ultrasound muscle thickness measurements for predicting fat-free mass in elderly population. J Nutr Health Aging. 2014;18(6):579-85. doi: 10.1007/s12603-013-0419-7.
- Shen W, Punyanitya M, Wang Z, Gallagher D, St-Onge MP, Albu J, Heymsfield SB, Heshka S. Visceral adipose tissue: relations between single-slice areas and total volume. Am J Clin Nutr. 2004 Aug;80(2):271-8. doi: 10.1093/ajcn/80.2.271.
- Sanada K, Kearns CF, Midorikawa T, Abe T. Prediction and validation of total and regional skeletal muscle mass by ultrasound in Japanese adults. Eur J Appl Physiol. 2006 Jan;96(1):24-31. doi: 10.1007/s00421-005-0061-0. Epub 2005 Oct 19.
- Paris MT, Mourtzakis M, Day A, Leung R, Watharkar S, Kozar R, Earthman C, Kuchnia A, Dhaliwal R, Moisey L, Compher C, Martin N, Nicolo M, White T, Roosevelt H, Peterson S, Heyland DK. Validation of Bedside Ultrasound of Muscle Layer Thickness of the Quadriceps in the Critically Ill Patient (VALIDUM Study). JPEN J Parenter Enteral Nutr. 2017 Feb;41(2):171-180. doi: 10.1177/0148607116637852. Epub 2016 Jul 11.
- Prado CM, Heymsfield SB. Lean tissue imaging: a new era for nutritional assessment and intervention. JPEN J Parenter Enteral Nutr. 2014 Nov;38(8):940-53. doi: 10.1177/0148607114550189. Epub 2014 Sep 19. Erratum In: JPEN J Parenter Enteral Nutr. 2016 Jul;40(5):742.
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
January 1, 2017
Primary Completion (Actual)
March 22, 2019
Study Completion (Anticipated)
September 1, 2019
Study Registration Dates
First Submitted
December 30, 2016
First Submitted That Met QC Criteria
May 17, 2017
First Posted (Actual)
May 19, 2017
Study Record Updates
Last Update Posted (Actual)
August 30, 2019
Last Update Submitted That Met QC Criteria
August 28, 2019
Last Verified
August 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1848/2016
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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