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Determining Energy Needs in Colorectal Cancer

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03131921
Acronym
RECODE
Enrollment
20
Registered
2017-04-27
Start date
2016-04-05
Completion date
2022-08-18
Last updated
2023-09-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer

Keywords

Energy expenditure, Nutrition, Colorectal cancer, Dietary needs

Brief summary

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.

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.

Interventions

None listed

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
University of Alberta
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Resting energy expenditureAt baseline, before or immediately beginning cancer treatmentTo assess resting energy expenditure using indirect calorimtery

Secondary

MeasureTime frameDescription
Body compositionAt baseline, before or immediately beginning cancer treatmentTo assess skeletal muscle and adipose tissue using computerized tomography images taken before beginning cancer treatment
Total energy expenditurePost-treatment, within 3 years after completion of cancer treatmentTo assess total energy expenditure (one time, over 14 days) using doubly labeled water and accelerometers

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026