Practice Based Nutrition Intervention-2 (PBNI-2)
Primary Purpose
Diabetes Mellitus, Type 2
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Vegan diet
American Diabetes Association guidelines
Sponsored by

About this trial
This is an interventional supportive care trial for Diabetes Mellitus, Type 2 focused on measuring Diabetes Mellitus, Type 2, Diet, Vegetarian, Diet, Fat-Restricted, Glycemic Index
Eligibility Criteria
Inclusion Criteria:
- a diagnosis of type 2 diabetes mellitus, as defined by a fasting plasma glucose concentration ≥126 mg/dl on 2 occasions or a prior physician's diagnosis of type 2 diabetes with the use of hypoglycemic medications for at least 6 months
- male or female
- A1c between 6.5% and 10.5%
- age at least 18 years
- ability and willingness to participate in all components of the study
- willingness to be assigned to either a low-fat, vegan diet or to standard care
- diabetes medications unchanged for 1 month prior to volunteering for the study
- patient of Dr. Mark Sklar
Exclusion Criteria:
- body mass index >45 kg/m2
- alcohol consumption of more than 2 drinks per day or the equivalent, episodic increased drinking (e.g., more than 2 drinks per day on weekends), or a history of alcohol abuse or dependency followed by any current use
- use of recreational drugs in the past 6 months (past drug use, if fully recovered, is not a criteria for exclusion)
- pregnancy
- history of severe mental illness (with current unstable status)
- likely to be disruptive in group sessions (as determined by research staff)
- Signs/symptoms of acute uncontrolled diabetes (including but not limited to polyuria, polydipsia, blurred vision, uncontrolled weight loss)
- unstable medical status
- already following a low-fat, vegetarian diet
- an inordinate fear of blood draws
- inability to maintain current medication regimen
- lack of English fluency
Sites / Locations
- Physicians Committee for Responsible Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Vegan Group
American Diabetes Association guidelines
Arm Description
Participants in the intervention group will follow a low-fat, vegan diet for 20 weeks, and will attend nutrition classes in the form of a weekly support group.
Participants will follow ADA diet according to ADA regulations. This group will also receive weekly nutrition classes.
Outcomes
Primary Outcome Measures
hemoglobin A1C (diabetes management)
Secondary Outcome Measures
Body Weight
Blood Pressure
Glucose
Comprehensive Metabolic Panel
Serum cholesterol and triacylglycerol concentrations
Urinary albumin and creatinine
Genotyping for Taq1 A and Taq1 B polymorphisms, and APOE (Apolipoprotein E)
Waist and hip circumference
Dietary Acceptability
3-day dietary records
International Physical Activity Questionnaire
Food Acceptability Questionnaire
Eating Inventory
CESD-R (Center for Epidemiologic Studies Depression Scale: Review and revision)
Beck Depression Inventory II (BDI-II)
Height
24-Hour Multi-Pass Dietary Recalls
Full Information
NCT ID
NCT01700868
First Posted
October 2, 2012
Last Updated
October 19, 2015
Sponsor
Physicians Committee for Responsible Medicine
1. Study Identification
Unique Protocol Identification Number
NCT01700868
Brief Title
Practice Based Nutrition Intervention-2
Acronym
PBNI-2
Official Title
Practice Based Nutrition Intervention-2
Study Type
Interventional
2. Study Status
Record Verification Date
October 2015
Overall Recruitment Status
Completed
Study Start Date
July 2014 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
July 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Physicians Committee for Responsible Medicine
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study aims to test hypotheses that are potentially important to diabetes management, with practical implications for reducing the medical, personal, and economic costs of the disease. Anticipated outcomes include reductions in glycosylated hemoglobin that are significantly greater than those achievable with current diet recommendations, reductions in medication use among many intervention-group participants, beneficial changes in body weight and serum lipid concentrations, and a demonstration of the acceptability of the intervention diet. Progress toward these goals could refine dietary guidance for individuals with diabetes, increase treatment expectations, and reduce the massive burden the disease currently imposes.
The study further attempts to translate a dietary intervention studied in a clinical research setting to a medical practice. This will contribute to developing a model for diabetes care that can be used widely.
Detailed Description
Specific Aim 1 tests the hypothesis that the nutrition intervention (low-fat, low-GI, vegan diet; henceforth called the 'vegan diet') improves glycemic control, body weight, plasma lipid concentrations, blood pressure, and indices of renal function in a within-group analysis.
Glycosylated hemoglobin is the primary dependent variable, as well as fasting plasma glucose and urinary albumin and creatinine concentrations. The within-group changes in these variables from baseline to week 20, one-year follow-up will be compared.
Specific Aim 2 tests the hypothesis that the vegan diet is more effective than standard nutrition care for improving glycemic control, body weight, plasma lipid concentrations, blood pressure, and indices of renal function in individuals with type 2 diabetes.
Glycosylated hemoglobin is the primary dependent variable, as well as fasting plasma glucose and urinary albumin and creatinine concentrations in both the intervention and control groups. The between-groups differences in the changes in these variables from baseline to week 20, and one-year follow-up will be compared.
Specific Aim 3 tests the hypothesis that the vegan diet is sustainable among individuals with type 2 diabetes for a 20-week period, with weekly classes, and in a follow-up period of one year with limited professional support.
This will be assessed by 3-day dietary records at weeks 0, 20 and one-year follow-up.
Specific Aim 4 tests the hypothesis that the vegan diet has an acceptability that is comparable to that of standard nutrition care among individuals with type 2 diabetes.
This hypothesis will be addressed by quantitatively assessing adherence to and acceptability of the intervention and control diets, using the 3-day dietary record, the Food Acceptability Questionnaire, and the Eating Inventory, as described below.
Specific Aim 5 tests the hypothesis that the effects of the dietary interventions on A1c and body weight are reduced in individuals with the A1 and B1 alleles of the DRD2 gene.
This will be assessed through Taq1 A1 and B1 genotype determination at baseline.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2
Keywords
Diabetes Mellitus, Type 2, Diet, Vegetarian, Diet, Fat-Restricted, Glycemic Index
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care Provider
Allocation
Randomized
Enrollment
15 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Vegan Group
Arm Type
Experimental
Arm Description
Participants in the intervention group will follow a low-fat, vegan diet for 20 weeks, and will attend nutrition classes in the form of a weekly support group.
Arm Title
American Diabetes Association guidelines
Arm Type
Active Comparator
Arm Description
Participants will follow ADA diet according to ADA regulations. This group will also receive weekly nutrition classes.
Intervention Type
Other
Intervention Name(s)
Vegan diet
Other Intervention Name(s)
Plant-based diet
Intervention Description
A diet devoid of any animal products. Low-fat, low-Glycemic Index, vegan diet.
Intervention Type
Other
Intervention Name(s)
American Diabetes Association guidelines
Other Intervention Name(s)
ADA
Intervention Description
Participants will follow individualized diet plans following ADA guidelines
Primary Outcome Measure Information:
Title
hemoglobin A1C (diabetes management)
Time Frame
20 weeks
Secondary Outcome Measure Information:
Title
Body Weight
Time Frame
20 Weeks
Title
Blood Pressure
Time Frame
20 Weeks
Title
Glucose
Time Frame
20 Weeks
Title
Comprehensive Metabolic Panel
Time Frame
20 Weeks & one-year follow up
Title
Serum cholesterol and triacylglycerol concentrations
Time Frame
20 Weeks
Title
Urinary albumin and creatinine
Time Frame
20 Weeks
Title
Genotyping for Taq1 A and Taq1 B polymorphisms, and APOE (Apolipoprotein E)
Time Frame
20 Weeks
Title
Waist and hip circumference
Time Frame
20 Weeks
Title
Dietary Acceptability
Time Frame
20 Weeks
Title
3-day dietary records
Time Frame
20 Weeks
Title
International Physical Activity Questionnaire
Time Frame
20 Weeks
Title
Food Acceptability Questionnaire
Time Frame
20 Weeks
Title
Eating Inventory
Time Frame
20 Weeks
Title
CESD-R (Center for Epidemiologic Studies Depression Scale: Review and revision)
Time Frame
20 Weeks
Title
Beck Depression Inventory II (BDI-II)
Time Frame
20 Weeks
Title
Height
Time Frame
20 Weeks
Title
24-Hour Multi-Pass Dietary Recalls
Time Frame
20 Weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
a diagnosis of type 2 diabetes mellitus, as defined by a fasting plasma glucose concentration ≥126 mg/dl on 2 occasions or a prior physician's diagnosis of type 2 diabetes with the use of hypoglycemic medications for at least 6 months
male or female
A1c between 6.5% and 10.5%
age at least 18 years
ability and willingness to participate in all components of the study
willingness to be assigned to either a low-fat, vegan diet or to standard care
diabetes medications unchanged for 1 month prior to volunteering for the study
patient of Dr. Mark Sklar
Exclusion Criteria:
body mass index >45 kg/m2
alcohol consumption of more than 2 drinks per day or the equivalent, episodic increased drinking (e.g., more than 2 drinks per day on weekends), or a history of alcohol abuse or dependency followed by any current use
use of recreational drugs in the past 6 months (past drug use, if fully recovered, is not a criteria for exclusion)
pregnancy
history of severe mental illness (with current unstable status)
likely to be disruptive in group sessions (as determined by research staff)
Signs/symptoms of acute uncontrolled diabetes (including but not limited to polyuria, polydipsia, blurred vision, uncontrolled weight loss)
unstable medical status
already following a low-fat, vegetarian diet
an inordinate fear of blood draws
inability to maintain current medication regimen
lack of English fluency
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Neal Barnard, MD
Organizational Affiliation
Physicians Committee for Responsible Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Physicians Committee for Responsible Medicine
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20016
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
9863851
Citation
Ornish D, Scherwitz LW, Billings JH, Brown SE, Gould KL, Merritt TA, Sparler S, Armstrong WT, Ports TA, Kirkeeide RL, Hogeboom C, Brand RJ. Intensive lifestyle changes for reversal of coronary heart disease. JAMA. 1998 Dec 16;280(23):2001-7. doi: 10.1001/jama.280.23.2001. Erratum In: JAMA 1999 Apr 21;281(15):1380.
Results Reference
background
PubMed Identifier
10496449
Citation
Esselstyn CB Jr. Updating a 12-year experience with arrest and reversal therapy for coronary heart disease (an overdue requiem for palliative cardiology). Am J Cardiol. 1999 Aug 1;84(3):339-41, A8. doi: 10.1016/s0002-9149(99)00290-8.
Results Reference
background
PubMed Identifier
10446033
Citation
Nicholson AS, Sklar M, Barnard ND, Gore S, Sullivan R, Browning S. Toward improved management of NIDDM: A randomized, controlled, pilot intervention using a lowfat, vegetarian diet. Prev Med. 1999 Aug;29(2):87-91. doi: 10.1006/pmed.1999.0529.
Results Reference
background
Learn more about this trial
Practice Based Nutrition Intervention-2
We'll reach out to this number within 24 hrs