Determining Energy Needs in Colorectal Cancer (RECODE)

September 1, 2023 updated by: University of Alberta

Resting Energy Expenditure in Cancer - Associations With Body Composition, Dietary Intake, and Exercise Habits

This is an observational study to assess the determinants of energy expenditure in cancer, and how those change throughout the disease trajectory. The investigators hypothesize that skeletal muscle will be the primary determinant of energy expenditure throughout the disease trajectory.

Study Overview

Status

Completed

Conditions

Detailed Description

Proper nutrition is a hallmark of successful cancer treatment. Adequate energy intake helps to maintain body weight and composition, improving outcomes such as response to therapy, quality of life, and survival. Unfortunately, little is known about energy needs in cancer, as few studies have assessed energy expenditure (the amount of calories used/day). Furthermore, individuals with cancer often experience muscle loss (sarcopenia), changes in physical activity, and undergo treatment, all of which might substantially alter energy needs. Equations to estimate energy REE (and thus dietary requirements) were created from cohorts of healthy individuals, and no tools that can be easily used in clinical settings are validated to assess REE.

The overarching aim of this study is to evaluate the largest component of energy needs - resting energy expenditure (REE) in relation to body composition (skeletal muscle, adipose tissue) and physical activity in a cohort of patients with colorectal cancer. Other aims will explore the changes in energy expenditure and determine the accuracy of a portable indirect calorimeter for measuring REE.

Newly-diagnosed individuals with stage II-IV colorectal cancer will undergo indirect calorimetry to assess REE. Body composition will be measured by CT scans, with sarcopenia status based on previously published cut-points. Nutritional status and inflammation (C-reactive protein, neutrophil:lymphocyte) will be assessed as confounding variables.

Total energy expenditure will be measured near treatment start in a sub-sample of 20 participants with colorectal cancer using doubly labeled water and accelerometers. Participants will wear accelerometers (ActiCal) for 14 days to provide detailed physical activity data.These assessments will also be preformed in a sub-sample of 20 participants after treatment end.

An additional part of this study will assess the validity of a portable indirect calorimeter for measuring REE. To address this, a sub-group of patients will be invited to undergo an additional test of REE using a portable indirect calorimeter, the FitMate (COSMED). Results will be compared using Pearson's correlation, dependent samples t-test, and Bland-Altman analysis to assess agreement between the FitMate and validated indirect calorimeters (VMax metabolic cart and whole body calorimtery unit). Exploratory outcomes include phase angle by bioelectrical impedance analysis, handgrip strength, calf circumference, and nutrition status by patient generated subjective global assessment (PG-SGA).

The results from this project will provide a basis of better energy recommendations to sustain body weight and composition, thereby improving prognosis in cancer.

Study Type

Observational

Enrollment (Actual)

20

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

    • Alberta
      • Edmonton, Alberta, Canada
        • Cross Cancer Institute
      • Edmonton, Alberta, Canada, T6G2E1
        • University of Alberta

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

18 years to 90 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

Patients with colorectal cancer (stage II-IV) at the Cross Cancer Institute (Edmonton, Alberta, Canada)

Description

Pre-treatment Participants:

Inclusion Criteria:

  • Recent diagnosis of colorectal cancer (stage II-IV);
  • Able to arrive at the Human Nutrition Research Unit fasted;
  • Patients undergoing treatment should be able to undergo measurements within 20 days of treatment commencement;
  • Able to provide written informed consent;
  • Able to communicate freely in English;
  • Age 18-90

Exclusion Criteria:

  • Recent (within the past month) anti-cancer therapy;
  • Recent invasive surgery (within the last 4 weeks);
  • Women during pregnancy or are breast-feeding;
  • Inability to breathe under the indirect calorimeter hood for 20-30 minutes;
  • Severe toxicity during the 1st cycle therapy (where applicable);
  • Severe mobility issues (e.g. confined to wheelchair);
  • Use of medications that may affect body composition or metabolism will be evaluated individually (e.g. cortico-steroids, hormone replacement, etc.)
  • Patients with a pacemaker

Post-treatment participants:

Inclusion Criteria

  • Recently (<3 year) completed adjuvant chemotherapy treatment for colorectal cancer (stage II-IV)
  • Able to arrive at the Human Nutrition Research Unit fasted
  • Able to provide written informed consent
  • Able to communicate freely in English
  • Age 18-90

Exclusion Criteria

  • Recent (within the past month) anti-cancer therapy
  • Recent invasive surgery (within the last 4 weeks)
  • Women during pregnancy or are breast-feeding
  • Inability to breathe under the indirect calorimeter hood for 20-30 minutes
  • Severe mobility issues (e.g. confined to wheelchair)
  • Use of medications that may affect body composition or metabolism will be evaluated individually (e.g. cortico-steroids, hormone replacement, etc.)
  • Patients with a pacemaker

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

Cohorts and Interventions

Group / Cohort
Colorectal cancer
No intervention. Patients with newly diagnosed stage II-IV colorectal cancer will be enrolled.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Resting energy expenditure
Time Frame: At baseline, before or immediately beginning cancer treatment
To assess resting energy expenditure using indirect calorimtery
At baseline, before or immediately beginning cancer treatment

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body composition
Time Frame: At baseline, before or immediately beginning cancer treatment
To assess skeletal muscle and adipose tissue using computerized tomography images taken before beginning cancer treatment
At baseline, before or immediately beginning cancer treatment
Total energy expenditure
Time Frame: Post-treatment, within 3 years after completion of cancer treatment
To assess total energy expenditure (one time, over 14 days) using doubly labeled water and accelerometers
Post-treatment, within 3 years after completion of cancer treatment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Carla M Prado, University of Alberta

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

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)

April 5, 2016

Primary Completion (Actual)

August 18, 2022

Study Completion (Actual)

August 18, 2022

Study Registration Dates

First Submitted

April 24, 2017

First Submitted That Met QC Criteria

April 24, 2017

First Posted (Actual)

April 27, 2017

Study Record Updates

Last Update Posted (Actual)

September 6, 2023

Last Update Submitted That Met QC Criteria

September 1, 2023

Last Verified

August 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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