search
Back to results

Effects of a High Protein Diet on Clinical Outcomes in Heart Failure

Primary Purpose

Heart Failure, Diabetes Mellitus

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
12-week supervised weight loss intervention
Sponsored by
University of California, Irvine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Heart Failure focused on measuring High Protein Diet in heart failure, obesity and heart failure, Weight management in Heart failure, heart failure, diabetes and obesity

Eligibility Criteria

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

Inclusion Criteria:

  • obese (BMI > 27 kg/m2);
  • history of type 2 DM or documented impaired fasting glucose (IFG) according to fasting plasma glucose levels of 100-125 mg/dl or meeting 3 out of 4 criteria or Metabolic Syndrome ( as defined by the International Diabetes Federation 2011
  • evaluation of HF and optimization of medical therapy; and
  • ischemic or idiopathic HF etiology.

Exclusion Criteria:

  • age ≤18 years old;
  • history of clinically significant illness including acute myocardial infarction or sustained ventricular arrhythmia in the prior 3 months or current liver, respiratory, and/or gastrointestinal disease and malignancy;
  • pregnancy or lactation;
  • serum creatinine level > 1.5 mg/dl;*
  • currently participating in a supervised weight loss program;
  • physician refusal to permit patient participation in the study; and
  • weight loss of >6% in the last 6 months
  • gout or history of gout

Sites / Locations

  • University of California Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

High Protein Group

Standard Protein Group

Arm Description

12-week supervised weight loss program consisting of a HP diet defined as 30% of energy from protein, 40% from carbohydrates and 30% from fat

12-week supervised weight loss program consisting of a SP diet defined as 15% of energy from protein, 55% from carbohydrates and 30% from fat

Outcomes

Primary Outcome Measures

Change from Baseline in adiposity (and body composition; i.e., % body fat))

Secondary Outcome Measures

Change from Baseline in lipid profiles (while controlling for statin drug dosage)
Change from Baseline in glycemic control and insulin resistance
Change from Baseline in peripheral blood circulation (as measured using peripheral arterial tonometry and plasma nitroxide measurement)
Change from Baseline in levels of quality of life

Full Information

First Posted
August 15, 2011
Last Updated
May 19, 2016
Sponsor
University of California, Irvine
Collaborators
University of California, Los Angeles
search

1. Study Identification

Unique Protocol Identification Number
NCT01423266
Brief Title
Effects of a High Protein Diet on Clinical Outcomes in Heart Failure
Official Title
Examining the Effects of a High Protein Diet on Adiposity and Cardiac Structure in Patients With Heart Failure, Obesity, and Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
December 2009 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Irvine
Collaborators
University of California, Los Angeles

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This research project was designed to study the role of dietary modifications in heart failure (HF) patients that suffer from type 2 diabetes mellitus and obesity. Specifically, the purpose of this study is to determine whether or not heart failure patients participating in a 3-month intensive lifestyle modification program of either a high protein (30 % of total calories from protein) group will have a significant improvement in weight reduction, quality of life and clinical outcomes compared to a standardized protein (15% of total calories from protein) group.
Detailed Description
Clinical management of heart failure (HF) related to obesity and diet recommendations currently lacks a strong scientific basis, and clinicians are divided in their approach to diet recommendations for this patient population. It has been shown that in extremely obese HF patients, weight reduction improves cardiac structure and function as well as functional status and symptomatology. Evidence on the impact of voluntary weight loss on improvement in survival in obese HF patients, however, is limited. The purpose of this study is to determine whether or not heart failure patients participating in a 3-month intensive lifestyle modification program of either a high protein (30% of total calories from protein) group will have a significant improvement in weight reduction, quality of life and clinical outcomes compared to a standardized protein (15% of total calories from protein) group. In addition to dietary interventions, participants in both groups with be given an exercise prescription and encouraged to exercise for 20-30 minutes at least 3-5 times each week as tolerated. They will also continue to receive usual medical care, advice and other support for their condition from their cardiologist or medical physician. Both sets of participants will utilize self-monitoring tools to assist with diet compliance and behavior change. These self-monitoring tools are mandatory and will be collected and analyzed. At each visit, subjects will also be asked to will also be asked to have their weight and waist circumference measured and, at select visits, they will provide a 24 hour recall to assess fullness with the overall diet. Subjects will be given a 3-day food (3DFR) record at baseline, which will be returned at the the 2-week, 4- week and 8-week visits, and will also complete the 3DFR at three months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Diabetes Mellitus
Keywords
High Protein Diet in heart failure, obesity and heart failure, Weight management in Heart failure, heart failure, diabetes and obesity

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
78 (Actual)

8. Arms, Groups, and Interventions

Arm Title
High Protein Group
Arm Type
Experimental
Arm Description
12-week supervised weight loss program consisting of a HP diet defined as 30% of energy from protein, 40% from carbohydrates and 30% from fat
Arm Title
Standard Protein Group
Arm Type
Active Comparator
Arm Description
12-week supervised weight loss program consisting of a SP diet defined as 15% of energy from protein, 55% from carbohydrates and 30% from fat
Intervention Type
Procedure
Intervention Name(s)
12-week supervised weight loss intervention
Other Intervention Name(s)
weight management, diet, nutritional supervision
Intervention Description
Patients in the 2 study arms will participate in an intensive 12-week supervised weight loss intervention and will be seen by the same dietician at regular intervals: baseline, 2 weeks, 4 weeks, 8 weeks, and 12 weeks. Participants will receive personalized nutrition counseling and support during each of these visits. Participants will be randomized to either the HP or SP diet and assigned to receive one of two standard structured energy-restricted meal plans (1200, 1500 Kcal/day) based on the computed calorie deficit
Primary Outcome Measure Information:
Title
Change from Baseline in adiposity (and body composition; i.e., % body fat))
Time Frame
3 months and 15 months
Secondary Outcome Measure Information:
Title
Change from Baseline in lipid profiles (while controlling for statin drug dosage)
Time Frame
3 months and 15 months
Title
Change from Baseline in glycemic control and insulin resistance
Time Frame
3 months and 15 months
Title
Change from Baseline in peripheral blood circulation (as measured using peripheral arterial tonometry and plasma nitroxide measurement)
Time Frame
3 months and 15 months
Title
Change from Baseline in levels of quality of life
Time Frame
3 months and 15 months
Other Pre-specified Outcome Measures:
Title
Change in Cardiac Structure
Time Frame
3 months and 15 months
Title
Change in Cardiac Function
Time Frame
3 months and 15 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: obese (BMI > 27 kg/m2); history of type 2 DM or documented impaired fasting glucose (IFG) according to fasting plasma glucose levels of 100-125 mg/dl or meeting 3 out of 4 criteria or Metabolic Syndrome ( as defined by the International Diabetes Federation 2011 evaluation of HF and optimization of medical therapy; and ischemic or idiopathic HF etiology. Exclusion Criteria: age ≤18 years old; history of clinically significant illness including acute myocardial infarction or sustained ventricular arrhythmia in the prior 3 months or current liver, respiratory, and/or gastrointestinal disease and malignancy; pregnancy or lactation; serum creatinine level > 1.5 mg/dl;* currently participating in a supervised weight loss program; physician refusal to permit patient participation in the study; and weight loss of >6% in the last 6 months gout or history of gout
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lorraine S Evangelista, PhD,RN,FAAN
Organizational Affiliation
University of California, Irvine
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California Medical Center
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data management and analysis is in progress.

Learn more about this trial

Effects of a High Protein Diet on Clinical Outcomes in Heart Failure

We'll reach out to this number within 24 hrs