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Pilot Study on the Effects of a Plant-Strong Diet on Cardiovascular Risk Factors

Primary Purpose

Hyperlipidemias, Overweight and Obesity, Diabetes

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
TeleMOVE!
Culinary Rx
Sponsored by
Phoenix VA Health Care System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hyperlipidemias focused on measuring Plant-based diet, Hyperlipidemia, Diabetes, Overweight, Veterans

Eligibility Criteria

18 Years - 89 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Inclusion criteria: U.S. Veterans only

    1. Age >18 and < 90
    2. BMI >25 and < 40
    3. Subject has hypertension, diabetes, hyperlipidemia, or overweight/obesity based upon recognized body mass index (BMI) standards) and an interest and desire to make a lifestyle change.Ability to tolerate two FDG-PET-MRI scans.
    4. Active telephone contact information (either land line or cell phone)
    5. No contraindication to be on a PSD.
    6. Access to transportation and a functioning kitchen
    7. The ability to prepare meals independently.
    8. Access to a computer or tablet with internet access
    9. Digital camera or Smartphone

For the FDG-PET-MRI subset/portion of the study, there are additional inclusion criteria:

Inclusion criteria:

  1. Pooled risk cohort score ≥ 7.5%.
  2. No contraindication to magnetic resonance imaging (moderate or severe claustrophobia, ferromagnetic materials, inability to lie flat for 30 minutes).

Exclusion Criteria:

  • 1. Significant unplanned weight loss within the last six months 2. BMI < 25 or > 40 3. Uncontrolled insulin-dependent diabetes with a current HbA1C of over 9% 4. Contraindication to undertake a PSD 5. Age <18 years old 6. Pregnancy/lactation 7. Taking prescribed weight loss medication(s) 8. Currently following a plant-strong diet, vegan, or medical weight loss program diet 9. Celiac disease diagnosed within the last six months 10. End-stage hepatic disease or renal disease requiring dialysis 11. Active cancer or receiving chemotherapy or radiation therapy 12. Active alcohol or substance abuse problems 13. History of eating disorders 14. Fasting triglyceride level above 350 mg/dL 15. Any psychological issues that prevent compliance 16. Unable to speak the English language 17. Have limited mobility 18. Homeless or in housing with limited kitchen access

For the FDG-PET-MRI subset/portion of the study, there are additional exclusion criteria:

  1. Inability to tolerate PET scans.
  2. Contraindication to magnetic resonance imaging (moderate or severe claustrophobia, ferromagnetic materials, inability to lie flat for 30 minutes)
  3. Women of childbearing potential who do not have medical documentation of surgically induced menopause.

Sites / Locations

  • Phoenix VA Health Care System

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

TeleMOVE!

Culinary Rx

Arm Description

Veterans randomized to the control arm will participate in TeleMOVE!, an arm of the Management of Overweight Veterans (MOVE!) program. TeleMOVE! is telehealth treatment program within the VA designed to improve the lives of Veterans by assisting with weight management and health promotion. This program includes daily interaction with in-home messaging technologies and clinician contact as needed

Veterans randomized to the experimental arm will participate in Culinary Rx. Culinary Rx is an online instructional cooking and nutrition course that healthcare professionals can prescribe to patients who need to transition away from a Standard American Diet to a more health-supportive, whole foods, plant-based lifestyle. In partnership with The Plantrician Project, this course will focus on teaching the foundational cooking skills needed for long-term behavioral change, coupled with lifestyle education around nutrition and resources that will help users successfully face the many challenges inherent to dietary change.

Outcomes

Primary Outcome Measures

Change in Low-density lipoprotein (LDL)
Fasting Low-density lipoprotein measured in milligrams per deciliter (mg/dl)

Secondary Outcome Measures

Change in Dietary pattern
Degree to which meat, fish, dairy and added oils are decreased or eliminated from the dietary pattern; as well as the degree to which the consumption of fruits and vegetables (particularly whole-foods) are increased from baseline intake.
Change in carotid plaque
Plaque volume
Change in aortic pulse wave velocity
aortic pulse wave velocity
Change in Total Cholesterol
Fasting total cholesterol measured in milligrams per deciliter (mg/dl)
Change in Weight
Weight in kilograms measured with subject in light clothing without shoes
Change in Hemoglobin A1C (HgbA1c)
Hemoglobin A1c measured as %

Full Information

First Posted
October 25, 2017
Last Updated
March 9, 2021
Sponsor
Phoenix VA Health Care System
Collaborators
Rouxbe Online Culinary School, Carl T. Hayden Medical Research Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT03330548
Brief Title
Pilot Study on the Effects of a Plant-Strong Diet on Cardiovascular Risk Factors
Official Title
Pilot Study on the Effects of a Plant-Strong Diet on Cardiovascular Risk Factors
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
July 9, 2015 (Actual)
Primary Completion Date
March 5, 2021 (Actual)
Study Completion Date
March 5, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Phoenix VA Health Care System
Collaborators
Rouxbe Online Culinary School, Carl T. Hayden Medical Research Foundation

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
The purpose of this study is to conduct a preliminary test of the effectiveness of various educational interventions to promote adoption of a whole-food, plant-strong diet and reduce specific cardiovascular risk factors in Veterans, and subsequently perform a preliminary pilot study on whether this dietary approach will change plaque inflammation and endothelial function.
Detailed Description
The purpose of this study is to conduct a preliminary test of the effectiveness of various educational interventions to promote adoption of a whole-food, plant-strong diet and reduce specific cardiovascular risk factors in Veterans, and subsequently perform a preliminary pilot study on whether this dietary approach will change plaque inflammation and endothelial function. The specific aims are to conduct a preliminary examination of: The feasibility of Veterans to adopt a whole-food, plant-strong diet within five weeks, following a plant-strong protocol, or within 90 days following a Plant Strong Diet (PSD) using Culinary Rx, or by TeleMOVE! (standard of care control). Feasibility factors will evaluate acceptability and practicality by a measure of the recruitment process, attrition rate, reasons for dropping, perceived benefit, and comparison of dietary pattern changes before and after the intervention. a. Acceptability of a plant-strong diet. (Part 1) The effectiveness of a five-week whole-food, plant-strong diet on participants': Cardiovascular risk factors: Low-Density Lipoprotein, (LDL-C), High-Density Lipoprotein (HDL), Triglycerides (TG), Total Cholesterol (T Chol), C-Reactive Protein (CRP), basic chemistry panel, blood pressure, weight, waist circumference, and percent body fat. Dietary pattern, particularly the degree to which meat, fish, dairy, and added oils are decreased or eliminated from the dietary pattern; as well as the degree to which the consumption of fruits and vegetables (particularly whole-food) are increased from baseline intake, and the nutrient composition (percent of calories from protein, fat, carbohydrate, and amount of fiber) of the diet changes. (Part 3) The effectiveness of completing Culinary Rx as compared to TeleMOVE! for 90 days on participants': Cardiovascular risk factors: Low-Density Lipoprotein, (LDL-C), High-Density Lipoprotein (HDL), Triglycerides (TG), Total Cholesterol (T Chol), HgbA1c, blood pressure, body mass index, weight, waist to hip ratio, and. medication usage (e.g., blood pressure, hypoglycemic, lipid lowering and anti-depressants). Dietary pattern, particularly the degree to which meat, fish, dairy, and added oils are decreased or eliminated from the dietary pattern; as well as the degree to which the consumption of fruits and vegetables (particularly whole-food) are increased from baseline intake, and the nutrient composition (percent of calories from protein, fat, carbohydrate, and amount of fiber) of the diet changes. Long-term lifestyle changes as measured by sustainability of dietary pattern and cardiovascular risk changes that occurred at 90 days and were still present at six months and one year, (excluding change in plaque inflammation and endothelial function). Establish the ability of Positron Emission Tomography 18F-fluorodeoxyglucose radiopharmaceutical and magnetic resonance imaging (PET FDG-MRI) to assess serial change in plaque inflammation and plaque volume (Part 2) and then perform a pilot test to assess whether a 90-day PSD using Culinary Rx, or TeleMOVE! reduces plaque inflammation using FDG uptake on PET scan and structural changes on MRI (Part 3). Correlation analysis of aortic/carotid FDG uptake versus Framingham risk score from consecutive subjects who underwent PET FDG for clinical indications at Phoenix VA from January 1, 2010-May 31, 2015. Change in aortic/carotid plaque FDG uptake, plaque volume and aortic pulse wave velocity (measure of aortic/arterial stiffness) at baseline and following 90-day PSD using Culinary Rx, or TeleMOVE! (pilot prospective study).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyperlipidemias, Overweight and Obesity, Diabetes
Keywords
Plant-based diet, Hyperlipidemia, Diabetes, Overweight, Veterans

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Subjects will be randomized 2:1 into Culinary Rx or TeleMOVE! prior to baseline measures. We plan to enroll a subset of the 80 participants to undergo a PET-MRI sub-study (total of 21 participants). This cohort requires participants to have a pooled cohort risk score of ≥ 7.5%, be willing and able to undergo FDG-PET-MRI. [The ACC/AHA pooled risk calculator utilizes information such as age, lipid profile, hypertension to estimate 10 year risk of ASCVD.
Masking
Outcomes Assessor
Masking Description
The assessor for the imaging studies will be blinded to the study arms of the subjects.
Allocation
Randomized
Enrollment
87 (Actual)

8. Arms, Groups, and Interventions

Arm Title
TeleMOVE!
Arm Type
Active Comparator
Arm Description
Veterans randomized to the control arm will participate in TeleMOVE!, an arm of the Management of Overweight Veterans (MOVE!) program. TeleMOVE! is telehealth treatment program within the VA designed to improve the lives of Veterans by assisting with weight management and health promotion. This program includes daily interaction with in-home messaging technologies and clinician contact as needed
Arm Title
Culinary Rx
Arm Type
Experimental
Arm Description
Veterans randomized to the experimental arm will participate in Culinary Rx. Culinary Rx is an online instructional cooking and nutrition course that healthcare professionals can prescribe to patients who need to transition away from a Standard American Diet to a more health-supportive, whole foods, plant-based lifestyle. In partnership with The Plantrician Project, this course will focus on teaching the foundational cooking skills needed for long-term behavioral change, coupled with lifestyle education around nutrition and resources that will help users successfully face the many challenges inherent to dietary change.
Intervention Type
Behavioral
Intervention Name(s)
TeleMOVE!
Intervention Description
Active comparator- telehealth treatment program for weight management and health promotion
Intervention Type
Behavioral
Intervention Name(s)
Culinary Rx
Intervention Description
Experimental Arm- An online instructional cooking and nutrition course to promote a whole-foods, plant-based lifestyle.
Primary Outcome Measure Information:
Title
Change in Low-density lipoprotein (LDL)
Description
Fasting Low-density lipoprotein measured in milligrams per deciliter (mg/dl)
Time Frame
90 days, 6 months and one year from baseline
Secondary Outcome Measure Information:
Title
Change in Dietary pattern
Description
Degree to which meat, fish, dairy and added oils are decreased or eliminated from the dietary pattern; as well as the degree to which the consumption of fruits and vegetables (particularly whole-foods) are increased from baseline intake.
Time Frame
90 days, 6 months and one year from baseline
Title
Change in carotid plaque
Description
Plaque volume
Time Frame
90 days from baseline
Title
Change in aortic pulse wave velocity
Description
aortic pulse wave velocity
Time Frame
90 days from baseline
Title
Change in Total Cholesterol
Description
Fasting total cholesterol measured in milligrams per deciliter (mg/dl)
Time Frame
90 days, 6 months and one year from baseline
Title
Change in Weight
Description
Weight in kilograms measured with subject in light clothing without shoes
Time Frame
90 days, 6 months and one year from baseline
Title
Change in Hemoglobin A1C (HgbA1c)
Description
Hemoglobin A1c measured as %
Time Frame
90 days, 6 months and one year from baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Inclusion criteria: U.S. Veterans only Age >18 and < 90 BMI >25 and < 40 Subject has hypertension, diabetes, hyperlipidemia, or overweight/obesity based upon recognized body mass index (BMI) standards) and an interest and desire to make a lifestyle change.Ability to tolerate two FDG-PET-MRI scans. Active telephone contact information (either land line or cell phone) No contraindication to be on a PSD. Access to transportation and a functioning kitchen The ability to prepare meals independently. Access to a computer or tablet with internet access Digital camera or Smartphone For the FDG-PET-MRI subset/portion of the study, there are additional inclusion criteria: Inclusion criteria: Pooled risk cohort score ≥ 7.5%. No contraindication to magnetic resonance imaging (moderate or severe claustrophobia, ferromagnetic materials, inability to lie flat for 30 minutes). Exclusion Criteria: 1. Significant unplanned weight loss within the last six months 2. BMI < 25 or > 40 3. Uncontrolled insulin-dependent diabetes with a current HbA1C of over 9% 4. Contraindication to undertake a PSD 5. Age <18 years old 6. Pregnancy/lactation 7. Taking prescribed weight loss medication(s) 8. Currently following a plant-strong diet, vegan, or medical weight loss program diet 9. Celiac disease diagnosed within the last six months 10. End-stage hepatic disease or renal disease requiring dialysis 11. Active cancer or receiving chemotherapy or radiation therapy 12. Active alcohol or substance abuse problems 13. History of eating disorders 14. Fasting triglyceride level above 350 mg/dL 15. Any psychological issues that prevent compliance 16. Unable to speak the English language 17. Have limited mobility 18. Homeless or in housing with limited kitchen access For the FDG-PET-MRI subset/portion of the study, there are additional exclusion criteria: Inability to tolerate PET scans. Contraindication to magnetic resonance imaging (moderate or severe claustrophobia, ferromagnetic materials, inability to lie flat for 30 minutes) Women of childbearing potential who do not have medical documentation of surgically induced menopause.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Diane J Parrington, PhD
Organizational Affiliation
Phoenix VA Health Care System
Official's Role
Principal Investigator
Facility Information:
Facility Name
Phoenix VA Health Care System
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85012
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
The study start date was before January 18, 2017, so no plan is in place.

Learn more about this trial

Pilot Study on the Effects of a Plant-Strong Diet on Cardiovascular Risk Factors

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