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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ANZCTR
Last refreshed on: 13 January 2020
Main ID:  ACTRN12614001279617
Date of registration: 05/12/2014
Prospective Registration: No
Primary sponsor: Dr Alexia Murphy
Public title: Body composition assessment of children undergoing treatment for cancer
Scientific title: Study to examine the body composition of children undergoing treatment for cancer
Date of first enrolment: 14/12/2004
Target sample size: 64
Recruitment status: Completed
URL:  https://anzctr.org.au/ACTRN12614001279617.aspx
Study type:  Observational
Study design:  Purpose: Natural history;Duration: Cross-sectional;Selection: Convenience sample;Timing: Prospective;  
Phase:  Not Applicable
Countries of recruitment
Australia
Contacts
Name: Dr Alexia Murphy   
Address:  Children's Nutrition Research Center Level 4 RCHF Building Herston Rd Royal Children's Hospital Herston QLD 4029 Australia
Telephone: +61733464994
Email: alexia.murphy@uq.edu.au
Affiliation: 
Name: Dr Alexia Murphy   
Address:  Children's Nutrition Research Center Level 4 RCHF Building Herston Rd Royal Children's Hospital Herston QLD 4029 Australia
Telephone: +61733464994
Email: alexia.murphy@uq.edu.au
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: 1) Being treated for cancer at Royal Children's Hospital
Exclusion criteria: 2) Too unwell to undergo testing

Age minimum: 5 Years
Age maximum: 18 Years
Gender: Both males and females
Health Condition(s) or Problem(s) studied
Cancer - Children's - Leukaemia & Lymphoma
Cancer - Children's - Brain
Cancer - Children's - Other
Cancer;
Cancer
Intervention(s)
All children participating in the study will have their height and weight measured on arrival at the centre. The Paediatric Oncology Assessment Tool will be completed before any body composition measurements are taken. Mid arm circumferences will be taken using a tape measure and following standard guidelines. Skinfolds will be measured using calibrated calipers and following the strict standard site protocol. Measurements will be taken at the biceps, triceps, subscapular and suprailiac sites.

Total body potassium (TBK) analysis will be performed using a shadow shield whole-body counter (Accuscan, Canberra Industries, MA, USA), which contains three sodium iodide crystal scintillation detectors arranged above a scanning bed. The crystals detect the 1.46MeV gamma rays being emitted by the potassium-40 (40K) found in the body. As a fixed proportion of the body’s potassium occurs as the natural isotope 40K, TBK can be determined. The measurement of TBK will require the subject to lie supine on a bed that is moved under the detectors. Two 1100sec scans will be performed for each subject with all personal metallic objects having been removed. Background and sensitivity checks will be completed daily and considered in each measurement, with TBK in grams being reported. Body cell mass (BCM) will then be calculated from TBK and adjusted for body size (BCM/HTp). BCM/HTp will be expressed as a Z score relative to laboratory reference data.

ADP measurement will be performed using the Bod Pod (registered trademark) Body Composition System, adhering to the manufacturer’s instructions (Life Measurement Inc, Concord, CA, USA; software version 1.69). Prior to each measurement, the Bod Pod will be calibrated at zero litres and with a standard calibration cylinder of 50
Primary Outcome(s)
Body Mass Index[During Treatment - cross sectional study]
Percent Fat using air displacement plethysmography (bodpod)[During treatment - cross sectional study]
Body Cell Mass using total body potassium counting[During treatment - Cross-sectional study]
Secondary Outcome(s)
Nil[Nil]
Secondary ID(s)
Nil known
Source(s) of Monetary Support
Children's Nutrition Research Centre, The University of Queensland
Secondary Sponsor(s)
Prof Peter Davies
Ethics review
Status: Approved
Approval date:
Contact:
Results
Results available:
Date Posted:
Date Completed:
URL:
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