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Can Protein Intake be Increased Using Whole Foods Post-treatment in Cancer Patients?

Primary Purpose

Cancer, Other Malnutrition

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
≥ 2 eggs in addition to usual diet for 8 weeks
≥ 2 eggs in addition to usual diet for 4 weeks
Sponsored by
University of Alberta
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cancer focused on measuring Cancer, Nutrition, Protein, post-chemotherapy, Recovery, food-related quality of life

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients must have the ability to read, understand, and sign an informed consent and must be willing to comply with study treatment and follow-up. ≥18 years of age Histopathologically confirmed cancer with receipt of a platinum chemotherapy during treatment; active treatment has concluded. Capable of volitional oral semi-solid intake at baseline; able to maintain oral intake over the trial. Exclusion Criteria: Fed by nasogastric tube, gastrostomy, or total parenteral nutrition Cancer of the brain, Cancer of the regions which impact an individual's ability to consume food. A known hypersensitivity / allergy to eggs. Enrolment in any other clinical protocol or investigational study that may interfere with study procedures. Poorly controlled chronic illnesses or other inflammatory diseases (e.g. Chronic Obstructive Pulmonary Disease(COPD), uncontrolled non-insulin dependent diabetes, rheumatoid arthritis). In a clinician opinion, patients who have medical conditions that could interfere with nutrient metabolism or absorption (e.g., short bowel syndrome, Crohn's disease, etc.)

Sites / Locations

  • University of AlbertaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Early Intervention

Delayed Intervention

Arm Description

Participants are expected to begin intervention immediately after the completion of treatment for a period of 8 weeks.

Participants are expected to begin intervention 4 weeks after the completion of the treatment, for a period of 4 weeks (weeks 5-8).

Outcomes

Primary Outcome Measures

Difference in mean cumulative protein intake between the two groups at 8 weeks.
Mean cumulative protein intake will be arrived at by normalizing protein intake in kilocalories by body weight in kilograms
Difference in mean cumulative protein intake within a group at 8 weeks for each group.
Mean cumulative protein intake will be arrived at by normalizing protein intake in kilocalories by body weight in kilograms

Secondary Outcome Measures

Change in Energy Intake
Energy intake can be described as energy intake in kilocalories normalized by body weight in kilograms.
Change in Body weight
in kilograms
Change in Quality of Life
Research and Development(RAND) Short Form 36-Item Health Survey 1.0 Minimum to Maximum score= 0 to 100 High Score indicates more favorable outcome.
Change in Nutritional status and Symptom severity.
Patient generated-subjective global assessment (PG-SGA), 0-9 point score, higher the score more severe the malnourishment. Edmonton Symptom Assessment Scale- Revised (ESAS-r, 0 to 10 Visual analog scale, higher the number more severe the symptom)
Change in Quality of Life related to malnutrition
Functional assessment of Anorexia-Cachexia Therapy 5 question Anorexia/ Cachexia subscale (FAACT A/C Subscale, Score Range= 0 to 20, Higher the score better the quality of life)
Change in Physical performance
Short physical performance battery (SPPB, Score range= 0 to 12, higher the score better the performance)

Full Information

First Posted
April 13, 2023
Last Updated
September 20, 2023
Sponsor
University of Alberta
Collaborators
Egg Farmers of Canada
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1. Study Identification

Unique Protocol Identification Number
NCT05859100
Brief Title
Can Protein Intake be Increased Using Whole Foods Post-treatment in Cancer Patients?
Official Title
Can Protein Intake be Increased Using Whole Foods Post-treatment in Cancer Patients?
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2023 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
April 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Alberta
Collaborators
Egg Farmers of Canada

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Cancer and its treatments often result in severe toxicities and side effects that, over the course of treatment, results in weight loss and depletion of key nutrients. Loss of muscle mass and strength during cancer treatment is a critical problem because it negatively affects patient response and tolerance to therapy and post-treatment recovery. To restore the nutritional status, it is imperative to stimulate muscle protein anabolism. Eggs are high quality protein source, popular and well tolerated by cancer patients. Therefore, the objective of this study is to determine whether a nutritional intervention of ≥2 eggs can aid in restoring nutritional status and improving immune function and quality of life of cancer patients' post-treatment. It is an 8- week randomised clinical trial with parallel arm assignment. Half of the participants will receive the nutritional intervention (Early Intervention) and the other half will be on standard of care or usual diet for first 4 weeks. Starting from week 5, all participants will receive the nutrition intervention till week 8 (Delayed Intervention). Dietary intake (foods and nutrients), cumulative protein intake (g protein/kg body weight), immunological measures, physical performance and quality of life has been planned to be assessed over time and between groups to evaluate the feasibility of an egg intervention in meeting recommended protein intakes for patients with cancer.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer, Other Malnutrition
Keywords
Cancer, Nutrition, Protein, post-chemotherapy, Recovery, food-related quality of life

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomly assigned to one of the two parallel arms (i.e., egg intervention arm and no intervention arm) for the first 4 weeks. Starting from week 5, the participants in the egg intervention arm will continue with the intervention till week 8 and the participants in the control arm will crossover to the intervention arm for weeks 5 to 8.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Early Intervention
Arm Type
Experimental
Arm Description
Participants are expected to begin intervention immediately after the completion of treatment for a period of 8 weeks.
Arm Title
Delayed Intervention
Arm Type
Other
Arm Description
Participants are expected to begin intervention 4 weeks after the completion of the treatment, for a period of 4 weeks (weeks 5-8).
Intervention Type
Other
Intervention Name(s)
≥ 2 eggs in addition to usual diet for 8 weeks
Intervention Description
Participants are expected to consume≥ 2 eggs per day in addition to usual diet for 8 weeks in early intervention arm, beginning immediately post-treatment.
Intervention Type
Other
Intervention Name(s)
≥ 2 eggs in addition to usual diet for 4 weeks
Intervention Description
Participants are expected to continue intake of regular diet beginning immediately at post-treatment recovery for a duration of 4 weeks, then crossover to nutritional intervention arm from weeks 5 to 8 of post-treatment recovery for a duration of 4 weeks.
Primary Outcome Measure Information:
Title
Difference in mean cumulative protein intake between the two groups at 8 weeks.
Description
Mean cumulative protein intake will be arrived at by normalizing protein intake in kilocalories by body weight in kilograms
Time Frame
From baseline at 8 weeks
Title
Difference in mean cumulative protein intake within a group at 8 weeks for each group.
Description
Mean cumulative protein intake will be arrived at by normalizing protein intake in kilocalories by body weight in kilograms
Time Frame
From baseline at 8 weeks
Secondary Outcome Measure Information:
Title
Change in Energy Intake
Description
Energy intake can be described as energy intake in kilocalories normalized by body weight in kilograms.
Time Frame
From baseline at 8 weeks
Title
Change in Body weight
Description
in kilograms
Time Frame
From baseline at 8 weeks
Title
Change in Quality of Life
Description
Research and Development(RAND) Short Form 36-Item Health Survey 1.0 Minimum to Maximum score= 0 to 100 High Score indicates more favorable outcome.
Time Frame
From baseline at 8 weeks
Title
Change in Nutritional status and Symptom severity.
Description
Patient generated-subjective global assessment (PG-SGA), 0-9 point score, higher the score more severe the malnourishment. Edmonton Symptom Assessment Scale- Revised (ESAS-r, 0 to 10 Visual analog scale, higher the number more severe the symptom)
Time Frame
From baseline at 8 weeks
Title
Change in Quality of Life related to malnutrition
Description
Functional assessment of Anorexia-Cachexia Therapy 5 question Anorexia/ Cachexia subscale (FAACT A/C Subscale, Score Range= 0 to 20, Higher the score better the quality of life)
Time Frame
From baseline at 8 weeks
Title
Change in Physical performance
Description
Short physical performance battery (SPPB, Score range= 0 to 12, higher the score better the performance)
Time Frame
From baseline at 8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients must have the ability to read, understand, and sign an informed consent and must be willing to comply with study treatment and follow-up. ≥18 years of age Histopathologically confirmed cancer with receipt of a platinum chemotherapy during treatment; active treatment has concluded. Capable of volitional oral semi-solid intake at baseline; able to maintain oral intake over the trial. Exclusion Criteria: Fed by nasogastric tube, gastrostomy, or total parenteral nutrition Cancer of the brain, Cancer of the regions which impact an individual's ability to consume food. A known hypersensitivity / allergy to eggs. Enrolment in any other clinical protocol or investigational study that may interfere with study procedures. Poorly controlled chronic illnesses or other inflammatory diseases (e.g. Chronic Obstructive Pulmonary Disease(COPD), uncontrolled non-insulin dependent diabetes, rheumatoid arthritis). In a clinician opinion, patients who have medical conditions that could interfere with nutrient metabolism or absorption (e.g., short bowel syndrome, Crohn's disease, etc.)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Vera Mazurak, PhD
Phone
780-492-8048
Email
vmazurak@ualberta.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Wendy Wismer, PhD
Email
wwismer@ualberta.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vera Mazurak, PhD
Organizational Affiliation
University of Alberta
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alberta
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2C8
Country
Canada
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
No

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Can Protein Intake be Increased Using Whole Foods Post-treatment in Cancer Patients?

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