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Feasibility of a Carbohydrate-restricted, High-fat Diet on Head and Neck Squamous Cell Carcinoma Outcomes (CRHF)

Primary Purpose

Head and Neck Squamous Cell Carcinoma

Status
Completed
Phase
Not Applicable
Locations
Palestinian Territory, occupied
Study Type
Interventional
Intervention
Carbohydrate-restricted, high-fat diet
Regular composition diet
Sponsored by
University of Illinois at Urbana-Champaign
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Head and Neck Squamous Cell Carcinoma focused on measuring non-metastatic

Eligibility Criteria

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

Inclusion Criteria:

  1. Newly diagnosed with non-metastatic cancer of the oral cavity, hypopharynx, oropharynx, or larynx
  2. Plan to receive definitive radiation treatment at Augusta Victoria Hospital (AVH) in East Jerusalem
  3. Age > 18
  4. Karnofsky Index of β‰₯70 %
  5. Normal liver and kidney function tests
  6. Able to understand and willingly sign a written informed consent document
  7. Lives in the West Bank or Gaza
  8. Has an oven/microwave and a refrigerator where they are staying
  9. Cancer stage 1-4 with no metastasis
  10. BMI > 20 kg/mΒ²

Exclusion Criteria:

  1. Those who do not meet the inclusion criteria
  2. Have metastatic disease
  3. Will receive a palliative treatment
  4. On insulin treatment or other diabetic treatment
  5. Uncontrolled illness (e.g. active infection, symptomatic CHF, cardiac arrhythmia, or psychiatric illness)
  6. Received previous treatment for another primary cancer
  7. Diagnosed with an illness that requires dietary modifications (e.g. renal disease, liver disease, celiac disease, and inflammatory bowel disease)
  8. Already consuming a carbohydrate-restricted, high-fat diet
  9. On chronic system corticosteroids for any reason (inhaled corticosteroids are allowed);
  10. Pregnant or lactating women
  11. Body mass index (BMI) < 20
  12. Will start treatment within <2 weeks from screening day
  13. Requires parenteral nutrition

Sites / Locations

  • Augusta Victoria Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

No Intervention

Arm Label

Arm A

Arm B

Control group

Arm Description

The experimental arm (N=6) were provided a CRHF diet with enough calories to maintain body weight for appoximately 2 weeks neoadjuvantly (during radiotherapy preparation) and adjuvantly during primary oncology treatment for ~6.5 weeks. The CRHF diet was composed of 45% fats (mostly) unsaturated fats, 25% proteins, and 30% carbohydrates.

Arm B (N=7) were provided a regular composition diet prescribed with enough calories to maintain body weight for approximately 2 weeks neoadjuvantly (during radiotherapy preparation) and adjuvantly during primary oncology treatment for ~6.5 weeks. The regular composition diet was composed of ~50-52% carbohydrates, ~30% fats, and 18-20% proteins,

The control group (N=26) followed applicable eligibility criteria but did not receive any intervention.

Outcomes

Primary Outcome Measures

Feasibility measure: Recruitment
Recruitment will be measured by recording the number of patients screened, included, excluded, dropped-out, and completed the study throughout the study period.
Feasibility measure: Adherence
Adherence will be measured by collecting daily food surveys that ask about daily food intake (checking the food items that have been consumed and providing information about any other additional foods that were consumed) as well as completing all study activities which are listed on a checklist.
Feasibility measure: Retention
Retention will be measured by recording the number of patients included or agreed to participate and completed all study protocol.
Blood Glucose
Blood glucose level was measured, recorded, and mentioned whether the level was normal, low, or high.
Complete blood count (CBC)
CBC levels were measured, recorded, and mentioned whether levels were normal, low, or high.
Liver function
Liver function tests were measured, recorded, and mentioned whether levels were normal, low, or high. These tests were done to assess whether liver function remained normal after consuming the diet or not. That was done by measuring the levels of GOT, GPT, and alkaline phosphatase in the blood and recording whether they were normal or not.
Kidney function
Kidney function tests were measured, recorded, and mentioned whether levels were normal, low, or high. These tests were done to assess whether kidney function remained normal after consuming the diet or not. That was done by measuring the levels of BUN, creatinine, and uric acid in the blood and recording whether they were normal or not.
Potassium
Potassium level was measured, recorded, and mentioned whether the level was normal, low, or high.
Phosphorus level was measured, recorded, and mentioned whether the level was normal, low, or high.
Phosphorus
Magnesium
Magnesium level was measured, recorded, and mentioned whether the level was normal, low, or high.
Sodium
Sodium level was measured, recorded, and mentioned whether the level was normal, low, or high.
Chloride
Chloride level was measured, recorded, and mentioned whether the level was normal, low, or high.
Calcium
Calcium level was measured, recorded, and mentioned whether the level was normal, low, or high.
Albumin level
Albumin level was measured, recorded, and mentioned whether the level was normal, low, or high.
C-reactive protein (CRP) level
CRP level was measured, recorded, and mentioned whether the level was normal, low, or high. High level indicates inflammation.
Total protein level
Total protein level was measured, recorded, and mentioned whether the level was normal, low, or high.
Insulin level
Insulin level was measured, recorded, and mentioned whether the level was normal, low, or high.
Triglycerides level
Triglycerides levels were measured, recorded, and mentioned whether the levels were normal, low, or high.
Total cholesterol level
Total cholesterol level was measured, recorded, and mentioned whether the level was normal, low, or high.
LDL-cholesterol level
LDL-cholesterol level was measured, recorded, and mentioned whether the level was normal, low, or high.
HDL-cholesterol level
HDL-cholesterol level was measured, recorded, and mentioned whether the level was normal, low, or high.

Secondary Outcome Measures

Tumor progression assessment
Tumor progression was assessed using RECIST and WHO criteria as well as diagnostic CTScan/ PETScan imaging.
Nutritional status assessment
Nutritional status was assessed using the "Patient generated subjective global assessment" (PG-SGA) tool.
Percentage of body fat
The percentage of body fat was measured by using a Bioelectric Impedance Analysis (BIA) device and used to study the effect of the intervention on body composition.
Percentage of lean body mass
The percentage of lean body mass was measured by using a Bioelectric Impedance Analysis (BIA) device and used to study the effect of the intervention on body composition.
Percentage of body water
The percentage of body water was measured by using a Bioelectric Impedance Analysis (BIA) device and used to study the effect of the intervention on body composition.
Basal metabolic rate (BMR)
BMR was measured by using a Bioelectric Impedance Analysis (BIA) device and used to study the effect of the intervention on body composition.
Quality of life assessment
Quality of life was assessed using EORTC QLQ questionnaires.
Symptom burden assessment
Symptom burden was assessed using the validated Memorial Symptom Assessment Survey.
Hospitalization
We recorded whether the participant was hospitalized or not.
Number of hospitalizations
If the participant was hospitalized, we recorded the number of hospitalizations
Duration of hospitalization
If the participant was hospitalized, we recorded the duration of each hospitalization
Weight loss
We recorded whether the participant had weight loss or not
Amount and span of weight loss
If the participant had weight loss, we recorded how much he had lost and during what time span
Treatment dose reduction
We recorded whether there was treatment dose reduction and the reason for that.
Treatment break
We recorded whether there was treatment break and the reason for that.
Early cessation of treatment
We recorded whether there was early cessation of treatment and the reason for that.

Full Information

First Posted
January 15, 2020
Last Updated
October 28, 2021
Sponsor
University of Illinois at Urbana-Champaign
Collaborators
Augusta Victoria Hospital, East Jerusalem
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1. Study Identification

Unique Protocol Identification Number
NCT04253808
Brief Title
Feasibility of a Carbohydrate-restricted, High-fat Diet on Head and Neck Squamous Cell Carcinoma Outcomes
Acronym
CRHF
Official Title
Feasibility of a Carbohydrate-restricted, High-fat Diet to Improve Outcomes in Head and Neck Squamous Cell Carcinoma: A Pilot Randomized Controlled Feeding Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
February 3, 2020 (Actual)
Primary Completion Date
August 10, 2021 (Actual)
Study Completion Date
August 10, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Illinois at Urbana-Champaign
Collaborators
Augusta Victoria Hospital, East Jerusalem

4. Oversight

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

5. Study Description

Brief Summary
This study will test the feasibility of a carbohydrate-restricted, high-fat (CRHF) diet intervention in newly diagnosed head and neck squamous cell carcinoma patients who will receive definitive radiation.
Detailed Description
Our previous observational research indicates that a pretreatment diet high in total carbohydrates is associated with increased risk of all-cause and disease-specific mortality in head and neck cancer. The purpose of this study is to conduct a single-blinded randomized controlled trial to test the feasibility of a carbohydrate-restricted, high-fat (CRHF) diet intervention in newly diagnosed head and neck cell squamous carcinoma (HNSCC) patients who will receive definitive radiation. The secondary aim is to collect preliminary data on the effect of the intervention on tumor progression, nutritional status, body composition, quality of life, and symptom burden. Thirteen newly diagnosed HNSCC non-metastatic patients were recruited from Augusta Victoria Hospital in East Jerusalem and randomized into one of two arms; a carbohydrate-restricted, high-fat diet arm (arm A) and a regular diet composition arm (Arm B). Arm A (N=6) were provided a CRHF diet both neoadjuvantly (for 2 weeks prior to treatment) and adjuvantly (during treatment with radiation). Arm B (N=7) received standard oncologic treatment including a regular diet (50-52% carbohydrates, 30% fats, and 18-20% proteins). Feasibility outcomes, including recruitment, retention, intervention adherence, and safety were tracked weekly. Biomarkers, tumor progression, nutritional status, body composition, QOL, and symptoms were assessed at baseline, 2-weeks, and 2-3 months post-treatment. A control group (N=26) included HNSCC patients who follow the same applicable eligibility criteria and did not receive any kind of dietary intervention. Medical information were collected retrospectively from the control group patients' files. Information on demographics (age, sex, smoking status, weight, height, marital status, education, occupation, and residency), tumor site, cancer stage, treatment dose reduction, treatment break, early cessation of treatment, hospitalization, symptoms, and weight loss, were collected during treatment from arms A and B and retrospectively from the control group. This proposed pilot/feasibility study is the first step in determining if a CRHF diet is an effective treatment modality in cancer and if providing a diet with any composition before and during treatment is more beneficial than not providing a diet at all.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Head and Neck Squamous Cell Carcinoma
Keywords
non-metastatic

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial
Masking
Participant
Masking Description
Participants will be blinded from the group they are assigned to.
Allocation
Randomized
Enrollment
39 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm A
Arm Type
Experimental
Arm Description
The experimental arm (N=6) were provided a CRHF diet with enough calories to maintain body weight for appoximately 2 weeks neoadjuvantly (during radiotherapy preparation) and adjuvantly during primary oncology treatment for ~6.5 weeks. The CRHF diet was composed of 45% fats (mostly) unsaturated fats, 25% proteins, and 30% carbohydrates.
Arm Title
Arm B
Arm Type
Active Comparator
Arm Description
Arm B (N=7) were provided a regular composition diet prescribed with enough calories to maintain body weight for approximately 2 weeks neoadjuvantly (during radiotherapy preparation) and adjuvantly during primary oncology treatment for ~6.5 weeks. The regular composition diet was composed of ~50-52% carbohydrates, ~30% fats, and 18-20% proteins,
Arm Title
Control group
Arm Type
No Intervention
Arm Description
The control group (N=26) followed applicable eligibility criteria but did not receive any intervention.
Intervention Type
Behavioral
Intervention Name(s)
Carbohydrate-restricted, high-fat diet
Other Intervention Name(s)
CRHF diet
Intervention Description
Diet composition was ~45% fats, ~30% carbohydrates, and ~25% proteins. Calorie needs were provided according to what the Bioelectrical Impedance (BIA) device gave as required to maintain bodyweight. Sources of macronutrients: Carbohydrates: from whole grains, dairy products, legumes, fruits, and vegetables. Fats: from mono- and polyunsaturated fatty acids, including medium- and long-chain fatty acids. Proteins: plant-based proteins and lean animal-based proteins. All meals were provided to the participants throughout the study period and the diet was provided orally unless the patient was on a feeding tube or a feeding tube is ordered by a physician during the study period. Diet texture was according to patients chewing and swallowing abilities. If the patient is on a feeding tube or intake is insufficient, a formula with similar macronutrient composition + a protein supplement was provided.
Intervention Type
Behavioral
Intervention Name(s)
Regular composition diet
Intervention Description
The regular composition diet contained approximately 50-52% carbohydrates, 30% fats, and 18-20% proteins
Primary Outcome Measure Information:
Title
Feasibility measure: Recruitment
Description
Recruitment will be measured by recording the number of patients screened, included, excluded, dropped-out, and completed the study throughout the study period.
Time Frame
Through study completion, an average of 2 years
Title
Feasibility measure: Adherence
Description
Adherence will be measured by collecting daily food surveys that ask about daily food intake (checking the food items that have been consumed and providing information about any other additional foods that were consumed) as well as completing all study activities which are listed on a checklist.
Time Frame
Throughout the 16.5 week study period (from baseline till the end of study)
Title
Feasibility measure: Retention
Description
Retention will be measured by recording the number of patients included or agreed to participate and completed all study protocol.
Time Frame
Throughout 16.5 week study period (from baseline till the end of study)
Title
Blood Glucose
Description
Blood glucose level was measured, recorded, and mentioned whether the level was normal, low, or high.
Time Frame
Throughout the 8.5 weeks of intervention
Title
Complete blood count (CBC)
Description
CBC levels were measured, recorded, and mentioned whether levels were normal, low, or high.
Time Frame
Throughout the 8.5 weeks of intervention
Title
Liver function
Description
Liver function tests were measured, recorded, and mentioned whether levels were normal, low, or high. These tests were done to assess whether liver function remained normal after consuming the diet or not. That was done by measuring the levels of GOT, GPT, and alkaline phosphatase in the blood and recording whether they were normal or not.
Time Frame
Throughout the 8.5 weeks of intervention
Title
Kidney function
Description
Kidney function tests were measured, recorded, and mentioned whether levels were normal, low, or high. These tests were done to assess whether kidney function remained normal after consuming the diet or not. That was done by measuring the levels of BUN, creatinine, and uric acid in the blood and recording whether they were normal or not.
Time Frame
Throughout the 8.5 weeks of intervention
Title
Potassium
Description
Potassium level was measured, recorded, and mentioned whether the level was normal, low, or high.
Time Frame
Throughout the 8.5 weeks of intervention
Title
Phosphorus level was measured, recorded, and mentioned whether the level was normal, low, or high.
Description
Phosphorus
Time Frame
Throughout the 8.5 weeks of intervention
Title
Magnesium
Description
Magnesium level was measured, recorded, and mentioned whether the level was normal, low, or high.
Time Frame
Throughout the 8.5 weeks of intervention
Title
Sodium
Description
Sodium level was measured, recorded, and mentioned whether the level was normal, low, or high.
Time Frame
Throughout the 8.5 weeks of intervention
Title
Chloride
Description
Chloride level was measured, recorded, and mentioned whether the level was normal, low, or high.
Time Frame
Throughout the 8.5 weeks of intervention
Title
Calcium
Description
Calcium level was measured, recorded, and mentioned whether the level was normal, low, or high.
Time Frame
Throughout the 8.5 weeks of intervention
Title
Albumin level
Description
Albumin level was measured, recorded, and mentioned whether the level was normal, low, or high.
Time Frame
Throughout the 8.5 weeks of intervention
Title
C-reactive protein (CRP) level
Description
CRP level was measured, recorded, and mentioned whether the level was normal, low, or high. High level indicates inflammation.
Time Frame
Throughout the 8.5 weeks of intervention
Title
Total protein level
Description
Total protein level was measured, recorded, and mentioned whether the level was normal, low, or high.
Time Frame
Throughout the 8.5 weeks of intervention
Title
Insulin level
Description
Insulin level was measured, recorded, and mentioned whether the level was normal, low, or high.
Time Frame
Throughout the 8.5 weeks of intervention
Title
Triglycerides level
Description
Triglycerides levels were measured, recorded, and mentioned whether the levels were normal, low, or high.
Time Frame
Throughout the 8.5 weeks of intervention
Title
Total cholesterol level
Description
Total cholesterol level was measured, recorded, and mentioned whether the level was normal, low, or high.
Time Frame
Throughout the 8.5 weeks of intervention
Title
LDL-cholesterol level
Description
LDL-cholesterol level was measured, recorded, and mentioned whether the level was normal, low, or high.
Time Frame
Throughout the 8.5 weeks of intervention
Title
HDL-cholesterol level
Description
HDL-cholesterol level was measured, recorded, and mentioned whether the level was normal, low, or high.
Time Frame
Throughout the 8.5 weeks of intervention
Secondary Outcome Measure Information:
Title
Tumor progression assessment
Description
Tumor progression was assessed using RECIST and WHO criteria as well as diagnostic CTScan/ PETScan imaging.
Time Frame
Throughout 16.5 week study period (from baseline till the end of study)
Title
Nutritional status assessment
Description
Nutritional status was assessed using the "Patient generated subjective global assessment" (PG-SGA) tool.
Time Frame
Throughout 16.5 week study period (from baseline till the end of study)
Title
Percentage of body fat
Description
The percentage of body fat was measured by using a Bioelectric Impedance Analysis (BIA) device and used to study the effect of the intervention on body composition.
Time Frame
Throughout 16.5 week study period (from baseline till the end of study)
Title
Percentage of lean body mass
Description
The percentage of lean body mass was measured by using a Bioelectric Impedance Analysis (BIA) device and used to study the effect of the intervention on body composition.
Time Frame
Throughout 16.5 week study period (from baseline till the end of study)
Title
Percentage of body water
Description
The percentage of body water was measured by using a Bioelectric Impedance Analysis (BIA) device and used to study the effect of the intervention on body composition.
Time Frame
Throughout 16.5 week study period (from baseline till the end of study)
Title
Basal metabolic rate (BMR)
Description
BMR was measured by using a Bioelectric Impedance Analysis (BIA) device and used to study the effect of the intervention on body composition.
Time Frame
Throughout 16.5 week study period (from baseline till the end of study)
Title
Quality of life assessment
Description
Quality of life was assessed using EORTC QLQ questionnaires.
Time Frame
Throughout 16.5 week study period (from baseline till the end of study)
Title
Symptom burden assessment
Description
Symptom burden was assessed using the validated Memorial Symptom Assessment Survey.
Time Frame
Throughout 16.5 week study period (from baseline till the end of study)
Title
Hospitalization
Description
We recorded whether the participant was hospitalized or not.
Time Frame
Throughout the 8.5 weeks of intervention
Title
Number of hospitalizations
Description
If the participant was hospitalized, we recorded the number of hospitalizations
Time Frame
Throughout the 8.5 weeks of intervention
Title
Duration of hospitalization
Description
If the participant was hospitalized, we recorded the duration of each hospitalization
Time Frame
Throughout the 8.5 weeks of intervention
Title
Weight loss
Description
We recorded whether the participant had weight loss or not
Time Frame
Throughout 16.5 week study period (from baseline till the end of study)
Title
Amount and span of weight loss
Description
If the participant had weight loss, we recorded how much he had lost and during what time span
Time Frame
Throughout 16.5 week study period (from baseline till the end of study)
Title
Treatment dose reduction
Description
We recorded whether there was treatment dose reduction and the reason for that.
Time Frame
Throughout the 6.5 weeks of treatment
Title
Treatment break
Description
We recorded whether there was treatment break and the reason for that.
Time Frame
Throughout the 6.5 weeks of treatment
Title
Early cessation of treatment
Description
We recorded whether there was early cessation of treatment and the reason for that.
Time Frame
Throughout the 8.5 weeks of treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Newly diagnosed with non-metastatic cancer of the oral cavity, hypopharynx, oropharynx, or larynx Plan to receive definitive radiation treatment at Augusta Victoria Hospital (AVH) in East Jerusalem Age > 18 Karnofsky Index of β‰₯70 % Normal liver and kidney function tests Able to understand and willingly sign a written informed consent document Lives in the West Bank or Gaza Has an oven/microwave and a refrigerator where they are staying Cancer stage 1-4 with no metastasis BMI > 20 kg/mΒ² Exclusion Criteria: Those who do not meet the inclusion criteria Have metastatic disease Will receive a palliative treatment On insulin treatment or other diabetic treatment Uncontrolled illness (e.g. active infection, symptomatic CHF, cardiac arrhythmia, or psychiatric illness) Received previous treatment for another primary cancer Diagnosed with an illness that requires dietary modifications (e.g. renal disease, liver disease, celiac disease, and inflammatory bowel disease) Already consuming a carbohydrate-restricted, high-fat diet On chronic system corticosteroids for any reason (inhaled corticosteroids are allowed); Pregnant or lactating women Body mass index (BMI) < 20 Will start treatment within <2 weeks from screening day Requires parenteral nutrition
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anna E Arthur, PhD, MPH
Organizational Affiliation
University of Illinois at Urbana-Champaign
Official's Role
Principal Investigator
Facility Information:
Facility Name
Augusta Victoria Hospital
City
East Jerusalem
Country
Palestinian Territory, occupied

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Citations:
PubMed Identifier
29604042
Citation
Arthur AE, Goss AM, Demark-Wahnefried W, Mondul AM, Fontaine KR, Chen YT, Carroll WR, Spencer SA, Rogers LQ, Rozek LS, Wolf GT, Gower BA; University of Michigan Head and Neck SPORE Program. Higher carbohydrate intake is associated with increased risk of all-cause and disease-specific mortality in head and neck cancer patients: results from a prospective cohort study. Int J Cancer. 2018 Sep 1;143(5):1105-1113. doi: 10.1002/ijc.31413. Epub 2018 Apr 17.
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Feasibility of a Carbohydrate-restricted, High-fat Diet on Head and Neck Squamous Cell Carcinoma Outcomes

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