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Clinical Trials/NCT01998152
NCT01998152
Completed
N/A

The Effect of Individualized NUTritional Counselling on Muscle Mass and Treatment Outcome in Patients With Metastatic COLOrectal Cancer Undergoing Chemotherapy: the COLONUT Study

Amsterdam UMC, location VUmc5 sites in 1 country107 target enrollmentNovember 2013

Overview

Phase
N/A
Intervention
Not specified
Conditions
Stage IV Colorectal Cancer
Sponsor
Amsterdam UMC, location VUmc
Enrollment
107
Locations
5
Primary Endpoint
Change in skeletal muscle area (cm2) between individualized nutritional counselling versus usual nutritional care
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The purpose is to study the effect of individualized nutritional counselling compared to usual nutritional care on cross-sectional muscle area in patients with stage IV colorectal cancer during first line chemotherapy. Secondary, effect on total lean body mass, treatment intensity, physical functioning, quality of life and survival will be studied.We hypothesize that patients in the intervention arm benefit from individualized nutritional counseling.

Registry
clinicaltrials.gov
Start Date
November 2013
End Date
December 15, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Amsterdam UMC, location VUmc
Responsible Party
Principal Investigator
Principal Investigator

M.A.E van Bokhorst - de van der Schueren, Dr.

Senior Investigator dietetics and nutrition sciences Vumc

Amsterdam UMC, location VUmc

Eligibility Criteria

Inclusion Criteria

  • Age ≥18 years
  • Stage IV colorectal cancer
  • Scheduled for treatment with first line chemotherapy, either CAPOX(-B), FOLFOX(-B) or capecitabine(-B)
  • CT scan suitable for evaluating muscle mass at L3 level
  • Understanding of the Dutch language
  • Able and willing to give written informed consent

Exclusion Criteria

  • Chemotherapy in the previous three months
  • WHO performance status ≥ 3
  • Long-term high dose of corticosteroids: ≥ three weeks ≥ ten milligram prednisolon or equivalent

Outcomes

Primary Outcomes

Change in skeletal muscle area (cm2) between individualized nutritional counselling versus usual nutritional care

Time Frame: During 9 weeks of first line chemotherapy

will be measured with SliceOmatic software V5.0 (Tomovision) with use of routinely conducted CT scans for diagnostic and disease evaluation purposes

Secondary Outcomes

  • Change in total body lean body mass and segmental lean body mass (DEXA) in patients with stage IV colorectal cancer during 9 weeks of first line chemotherapy between individualized nutritional counseling versus usual nutritional care(During 9 weeks of first line chemotherapy)
  • Change in skeletal muscle area in patients with stage IV colorectal cancer during 20 weeks of first line chemotherapy between individualized nutritional counseling.versus usual nutritional care.(During 20 weeks of first line chemotherapy)
  • Associations of (changes in) muscle area with (changes in) mid-upper arm muscle circumference, whole body fat free mass (BIA) and whole body lean body mass (DEXA).(During 9 weeks of first line chemotherapy)
  • Composite of treatment toxicity, treatment intensity, treatment outcome, survival, physical functioning, quality of life and hand grip strength of both study arms(During 9 weeks and during 20 weeks of first line chemotherapy)

Study Sites (5)

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