Effect of an Oral Supplement on the Total Energy and Protein Intake of Head and Neck Cancer Patients in the Last 2 Weeks of Radiation Therapy
Primary Purpose
Head and Neck Cancer
Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Nutritional Supplement
Sponsored by
About this trial
This is an interventional treatment trial for Head and Neck Cancer focused on measuring food, diet, oral supplement, head and neck cancer, radiation
Eligibility Criteria
Inclusion Criteria:
- 18 years or older
- diagnosed with head and neck cancer including the lip, oral cavity, salivary glands, paranasal sinuses, oropharynx, nasopharynx, hypopharynx, larynx and thyroid.
- all histologic types of cancer
- all tumour stages according to American Joint Committee for Cancer (AJCC) Staging
- all forms of RT including standard or investigational for head and neck cancers
- alert and mentally competent
- English speaking
Exclusion Criteria:
- an allergy or intolerance to any of the substances used in the nutrition supplement
- Type I or II diabetes mellitus
- renal insufficiency
- unable to swallow
- additional criteria of all forms of chemotherapy standard or investigational or combination of radiation/chemotherapy standard or investigational for head and neck cancers
Sites / Locations
Outcomes
Primary Outcome Measures
total energy and protein intake
Secondary Outcome Measures
Full Information
NCT ID
NCT00375700
First Posted
September 11, 2006
Last Updated
February 24, 2016
Sponsor
AHS Cancer Control Alberta
Collaborators
Cross Cancer Institute
1. Study Identification
Unique Protocol Identification Number
NCT00375700
Brief Title
Effect of an Oral Supplement on the Total Energy and Protein Intake of Head and Neck Cancer Patients in the Last 2 Weeks of Radiation Therapy
Official Title
Efficacy of an Oral Nutrition Supplement on the Total Caloric and Protein Intake of Head and Neck Cancer Patients During the Last 2 Weeks of Radiation Therapy
Study Type
Interventional
2. Study Status
Record Verification Date
March 2012
Overall Recruitment Status
Withdrawn
Study Start Date
November 2006 (undefined)
Primary Completion Date
January 2010 (Actual)
Study Completion Date
January 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AHS Cancer Control Alberta
Collaborators
Cross Cancer Institute
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
In this study, an oral nutrition supplement has been developed that take into consideration: the nutritional requirements, treatment side-effects and taste preferences of head and neck cancer patients; the acceptance of a supplement when experiencing radiation therapy side-effects; and the taste preferences of head and neck cancer patients which may affect the supplement intake. We hope to increase dietary intake during the last 2 weeks of radiation therapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Head and Neck Cancer
Keywords
food, diet, oral supplement, head and neck cancer, radiation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Dietary Supplement
Intervention Name(s)
Nutritional Supplement
Primary Outcome Measure Information:
Title
total energy and protein intake
Time Frame
Study completion
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 years or older
diagnosed with head and neck cancer including the lip, oral cavity, salivary glands, paranasal sinuses, oropharynx, nasopharynx, hypopharynx, larynx and thyroid.
all histologic types of cancer
all tumour stages according to American Joint Committee for Cancer (AJCC) Staging
all forms of RT including standard or investigational for head and neck cancers
alert and mentally competent
English speaking
Exclusion Criteria:
an allergy or intolerance to any of the substances used in the nutrition supplement
Type I or II diabetes mellitus
renal insufficiency
unable to swallow
additional criteria of all forms of chemotherapy standard or investigational or combination of radiation/chemotherapy standard or investigational for head and neck cancers
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cathy Kubrak, PhD
Organizational Affiliation
University of Alberta
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Effect of an Oral Supplement on the Total Energy and Protein Intake of Head and Neck Cancer Patients in the Last 2 Weeks of Radiation Therapy
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