Effects of a Whole-food, Plant-based Nutrition Program on BP and Potassium in Subjects With CKD

April 15, 2024 updated by: Scott Liebman, University of Rochester

Effects of an Education Program Emphasizing a Whole-food, Plant-based Nutrition Program on Blood Pressure and Blood Potassium Levels in Subjects With Chronic Kidney Disease

The purpose of this study is to determine if an educational program emphasizing a whole food plant based diet favorably impacts blood pressure while not significantly increasing blood potassium levels, by comparing a group of patients receiving the educational program with a control group of patients receiving no specific education.

Study Overview

Status

Completed

Detailed Description

The primary objective of this study is to test the hypothesis that educating hypertensive chronic kidney disease (CKD) stage 3 and 4 patients on the benefit of a whole food plant based (WFPB) diet in the context of a 15-day educational program ("Jumpstart program") will lead to improved blood pressure control and will not increase rates of hyperkalemia.

Other objectives:

A) To test the effect of the Jumpstart program on degree of uptake on a WFPB diet via a 3 day food recall.

B) To test the effect of the Jumpstart program on other important outcomes in CKD in the following domains:

  1. Body composition such as weight and body mass index (BMI).
  2. Quality of life.
  3. Laboratory tests including- serum levels of sodium, bicarbonate, chloride, Blood urea nitrogen, creatinine, calcium, phosphorus, magnesium, albumin, parathyroid hormone, fibroblast growth factor 23, lipids, C-reactive protein and erythrocyte sedimentation rate.

C) To test the effect of the Jumpstart program on quality of life in hypertensive CKD patients.

Study Type

Interventional

Enrollment (Actual)

43

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • New York
      • Rochester, New York, United States, 14642
        • University of Rochester Medical Center
      • Rochester, New York, United States, 14642
        • Clinical Research Center of the University of Rochester Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Age greater than 18 years
  • Subjects with CKD 3 and 4 (as determined by an estimated glomerular filtration rate of ≥ 15 ml/min but < 60 ml/min for at least three months)
  • Subjects with hypertension, defined as use of antihypertension medication:
  • Lack of significant proteinuria ( subjects will have a 24 hour urine protein value of < 500 mg or a spot protein to creatinine ratio of < 0.5 or a microalbumin to creatinine ratio < 300) within previous 3 months.
  • Fluent in English language
  • Able and willing to comply with the testing schedule and the meeting schedule of the Jumpstart
  • Able and willing to comply with dietary advice of whole-food plant based diet given during the educational session
  • Able and willing to give informed consent
  • Must have computer/internet access to participate in virtual Zoom educational sessions (intervention group only)

Exclusion Criteria:

  • Kidney disease requiring immunosuppressive therapy
  • Diabetes mellitus
  • Pregnancy
  • Life expectancy < 12 months
  • History of solid organ transplant or anticipated solid organ transplant in next 2 months
  • History of hyperkalemia: (two or more potassium levels ≥ 5.0 Meq/L or those requiring intervention for high potassium levels within the last six months)
  • Subjects with malabsorptive syndromes
  • Subjects with history of bariatric surgery or planned bariatric surgery in the next 2 months
  • Subjects on warfarin
  • Subjects with documented eating disorder at the time of consent
  • Allergy or intolerance of a plant-based or plant-derived food (gluten, soy, etc.)
  • Following a vegan diet in the six months prior to consent
  • Major surgery within 60 days prior to consent

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Jumpstart Educational Program

Jumpstart sessions on day 1, 2, 5, 8, 12, and 15. Tests at baseline and week 2 visit: blood pressure, height and weight measurements to calculate a body mass index, urine tests to assess antioxidant activity, quality of life questionnaire (~8 minutes to complete) about physical and mental symptoms, a 3-day food record to assess if participants are changing their diet over the course of the study, assessment of medication use.

Tests performed at day 1, day 8, and day 15: A small blood draw [about 1 teaspoon] to check chemistry levels, cholesterol, and markers of inflammation. Laboratory tests are reviewed once available, and participant contacted by the study team either by telephone or My Chart regarding clinically significant results that require intervention. If potassium levels are higher than 5.2 Meq/L, the study team contacts the participant or their alternate contact directly. For the intervention group, this is in addition to the finger-stick blood collection.

Jumpstart educational program:

https://www.rochesterlifestylemedicine.com/about-community-jumpstart/

Other Names:
  • Nutritional education program
No Intervention: Control group
Participants randomized to the control group continue to receive medical, dietary, and nutritional advice from their medical team as normal. The testing is the same testing as the intervention group and will be done at day 1, day 8, and day 15 of the study. They do not participate in the educational sessions during the study but will have the opportunity to participate in the program at no charge at the conclusion of the study.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mean change in systolic blood pressure
Time Frame: Baseline to day 15
Unit of measurement - mm Hg
Baseline to day 15
Mean change in diastolic blood pressure
Time Frame: Baseline to day 15
Unit of measurement - mm Hg
Baseline to day 15
Mean change in potassium levels
Time Frame: Baseline to day 15
Unit of measurement - mEq/L
Baseline to day 15
Proportion of participants developing hyperkalemia
Time Frame: Day 15
Percentage
Day 15

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mean Change in energy/day
Time Frame: Baseline to day 15
Unit of measurement - kcal/day. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in energy/kg of body mass
Time Frame: Baseline to day 15
Unit of measurement - kcal/kg/day. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in total fat
Time Frame: Baseline to day 15
Unit of measurement - grams. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in % calories from fat
Time Frame: Baseline to day 15
Unit of measurement - Percentage. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in % calories from carbohydrates
Time Frame: Baseline to day 15
Unit of measurement - Percentage. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in % calories from protein
Time Frame: Baseline to day 15
Unit of measurement - Percentage. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in Animal protein
Time Frame: Baseline to day 15
Unit of measurement - grams. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in Vegetable protein
Time Frame: Baseline to day 15
Unit of measurement - grams. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in cholesterol
Time Frame: Baseline to day 15
Unit of measurement - milligrams. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in Total dietary fiber
Time Frame: Baseline to day 15
Unit of measurement - grams. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in Total fiber per 1000 kcal
Time Frame: Baseline to day 15
Unit of measurement - Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in calcium
Time Frame: Baseline to day 15
Unit of measurement - milligrams. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in phosphorous
Time Frame: Baseline to day 15
Unit of measurement - milligrams. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in magnesium
Time Frame: Baseline to day 15
Unit of measurement - milligrams. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in sodium
Time Frame: Baseline to day 15
Unit of measurement - milligrams. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in potassium
Time Frame: Baseline to day 15
Unit of measurement - milligrams. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in body mass
Time Frame: Baseline to day 15
Unit of measurement - kilograms. Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in body mass index
Time Frame: Baseline to day 15
Unit of measurement - kg/m². Subjects completed a 3-day food record prior to intervention and during Jumpstart (or equivalent time for controls). Participants were given a recording form, and verbal and written instructions to record relevant details for all foods and beverages consumed. Portion size was estimated, using food visual aids, or measured, using weight scales or volume measures. A research dietitian (NW) provided the food record instruction and reviewed the completed records with participants to increase the quality of the report. The food record data was then entered into the Nutrition Data System for Research (NSDR, Nutrition Coordinating Center, University of Minnesota, Twin Cities) for calculation of nutrient intake.
Baseline to day 15
Mean change in sodium measured in blood
Time Frame: Baseline to day 15
Unit of measurement - mEq/L
Baseline to day 15
Mean change in chloride measured in blood
Time Frame: Baseline to day 15
Unit of measurement - mEq/L
Baseline to day 15
Mean change in bicarbonate measured in blood
Time Frame: Baseline to day 15
Unit of measurement - mEq/L
Baseline to day 15
Mean change in blood urea nitrogen (BUN) measured
Time Frame: Baseline to day 15
Unit of measurement - mg/dl
Baseline to day 15
Mean change in creatinine measured in blood
Time Frame: Baseline to day 15
Unit of measurement - mg/dl
Baseline to day 15
Mean change in glucose measured in blood
Time Frame: Baseline to day 15
Unit of measurement - mg/dl
Baseline to day 15
Mean change in calcium measured in blood
Time Frame: Baseline to day 15
Unit of measurement - mg/dl
Baseline to day 15
Mean change in phosphorous measured in blood
Time Frame: Baseline to day 15
Unit of measurement - mg/dl
Baseline to day 15
Mean change in parathyroid hormome (PTH) measured in blood
Time Frame: Baseline to day 15
Unit of measurement - pg/mL
Baseline to day 15
Mean change in albumin measured in blood
Time Frame: Baseline to day 15
Unit of measurement - pg/mL
Baseline to day 15
Mean change in magnesium measured in blood
Time Frame: Baseline to day 15
Unit of measurement - mEq/L
Baseline to day 15
Mean change in erythrocyte sedimentation rate (ESR) measured in blood
Time Frame: Baseline to day 15
Unit of measurement - mm/hr
Baseline to day 15
Mean change in fibroblast growth factor (FGF)-23 measured in blood
Time Frame: Baseline to day 15
Unit of measurement - RU/ml
Baseline to day 15
Mean change in total cholesterol measured in blood
Time Frame: Baseline to day 15
Unit of measurement - mg/dl
Baseline to day 15
Mean change in low density lipoprotein (LDL) measured in blood
Time Frame: Baseline to day 15
Unit of measurement - mg/dl
Baseline to day 15
Mean change in high density lipoprotein (HDL) measured in blood
Time Frame: Baseline to day 15
Unit of measurement - mg/dl
Baseline to day 15
Mean change in triglycerides measured in blood
Time Frame: Baseline to day 15
Unit of measurement - mg/dl
Baseline to day 15
Mean change in 8-isoprostane measured in urine
Time Frame: Baseline to day 15
Unit of measurement - (ng/mg of creat)/kg
Baseline to day 15
Mean change in symptoms
Time Frame: Baseline to day 15

Higher scores indicate better health. Scores are transformed linearly to 0-100 range.

The symptom list assesses the extent of bother (not at all, somewhat, moderately, very much, extremely) during the last 30 days in terms of issues particularly relevant to patients with kidney disease including soreness in muscles, pain (joint,back, chest), headaches, cramps during dialysis, bruising, itchy skin, shortness of breath, dizziness, lack of appetite, excessive thirst, numbness in hands or feet, trouble with memory, blurred vision, nausea, or other problems with the access site.

Baseline to day 15
Mean change in effects of kidney disease
Time Frame: Baseline to day 15

Higher scores indicate better health. Scores are transformed linearly to 0-100 range.

Effects of kidney disease on daily life were assessed using the same five-point response scale used for the symptom/problem list and included restrictions on fluid and dietary intake, and impact on work, carrying out family responsibilities, travel, lifting objects, personal appearance, and time available to get things done.

Baseline to day 15
Mean change in burden of kidney disease
Time Frame: Baseline to day 15

Higher scores indicate better health. Scores are transformed linearly to 0-100 range.

The burden of kidney disease scale assesses perceptions of frustration and interference of kidney disease in one's life using a definitely true to definitely false response scale (interferes too much with life, too much time spent dealing with it, feel frustrated dealing with it, feel like a burden on family).

Baseline to day 15
Mean change in Medical Outcomes Study Short Form (MOS SF-12) physical composite
Time Frame: Baseline to day 15

Higher scores indicate better health. Scores are transformed linearly to 0-100 range.

Physical composite includes questions on how you feel about your physical health. In the survey, participants are asked if they could do things like climb stairs, move a table, or push a vacuum. How well they think they feel physically is a key measure of their health.

Baseline to day 15
Mean change in Medical Outcomes Study Short Form (MOS SF-12) mental composite
Time Frame: Baseline to day 15

Higher scores indicate better health. Scores are transformed linearly to 0-100 range.

Mental composite includes questions about general health, activity limits, ability to accomplish desired tasks, depression and anxiety, energy level, and social activities.

Baseline to day 15

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 26, 2020

Primary Completion (Actual)

December 12, 2022

Study Completion (Actual)

December 12, 2022

Study Registration Dates

First Submitted

March 26, 2024

First Submitted That Met QC Criteria

April 1, 2024

First Posted (Actual)

April 2, 2024

Study Record Updates

Last Update Posted (Actual)

April 17, 2024

Last Update Submitted That Met QC Criteria

April 15, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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