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Nutrigenomics: Personalizing Weight Loss for Obese Veterans

Primary Purpose

Obesity

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Personalized Genomics
Usual Care
Sponsored by
University of California, San Diego
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring veteran, obesity, personalized genomics

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Veterans able to receive care at the VASDHS and planning to start the MOVE! program.
  2. Veterans able to understand and consent to the study.
  3. BMI equal to or greater than 30 kg/m2.

Exclusion Criteria:

  1. Veterans unable to receive care at the VASDHS.
  2. Veterans unable to understand the consent process at the discretion of the PI.
  3. Active substance abuse or substance dependence disorder
  4. Cognitive disorder, psychiatric hospitalization in past 6-months, or presence of suicidal ideation identified on self-report instruments
  5. Bradycardia, rapid heart rate or other arrhythmia or active ischemia by EKG.
  6. Uncontrolled thyroid disease as measured by a TSH above or below the normal range.
  7. Body mass index < 30 kg/m2.
  8. Chronic kidney disease stage III or higher by National Kidney Foundation criteria (GFR = 30-59 ml/min).
  9. New York Heart Association's functional classification of congestive heart failure above Class I (not limited with normal physical activity by symptoms; Class II occurs when ordinary physical activity results in fatigue, dyspnea, or other symptoms).
  10. Sodium or potassium outside the normal range.
  11. Edema requiring the use of daily diuresis with furosemide, bumex or other diuretic (does not include hydrochlorthiazide).
  12. The use of high dose oral corticosteroids (above replacement doses).
  13. Veterans deficient in 25-OH vitamin D (<20 units/dl).
  14. Veterans with fasting LDL > 190 mg/dl.
  15. Veterans with fasting triglyceride levels > 1000 mg/dl.
  16. Excessive caffeine use (>6 caffeinated beverages/days).
  17. Prior gastrointestinal surgery with the exception of distal appendectomy.
  18. Acute infections or current use of antibiotic therapy.

Sites / Locations

  • VA San Diego Healthcare System

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Usual Care

Personalized Genomics

Arm Description

Usual care for veterans as part of the MOVE! program

Personalized genomics information from the FIT Test, Pathway Genomics

Outcomes

Primary Outcome Measures

Number of Participants With Weight Loss of 5% or More at 8 Weeks
Our primary hypotheses are that more obese veterans in the MOVE! program will lose greater or equal to 5% of their weight if they receive personalized genomic information and a genomically-derived diet built around packaged meals when compared to veterans in the same program that receive usual care during MOVE! and packaged meals after 8 weeks.

Secondary Outcome Measures

Number of Participants With Weight Loss of 5% or More at 24 Weeks
We hypothesize that more veterans in the genomic group that lose greater or equal to 5% weight loss at 8 weeks will maintain this weight loss after 24 weeks compared to veterans in the usual care group.

Full Information

First Posted
May 17, 2013
Last Updated
March 19, 2021
Sponsor
University of California, San Diego
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1. Study Identification

Unique Protocol Identification Number
NCT01859403
Brief Title
Nutrigenomics: Personalizing Weight Loss for Obese Veterans
Official Title
Nutrigenomics: Personalizing Weight Loss for Obese Veterans
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
November 2012 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
March 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Diego

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study aims to determine if providing genomic information to veterans can help them lose weight compared to usual care.
Detailed Description
About 35% of veterans are obese. The MOVE! program is a nation-wide 8-week program of group classes nationally to help obese veterans lose weight. While the program is successful for some veterans, about 75% of veterans are unable to lose ≥5% of their weight 24 weeks after MOVE! New methods are needed to help obese veterans seeking weight loss. Using personalized genomic information dictating a specific diet, and information on exercise and eating behaviors, may be one means to help promote weight loss. Just a single nucleotide change or polymorphism (SNP) in a gene can increase a person's risk for obesity, or change their lipid profile in response to the consumption of different macronutrients such as of fats or carbohydrates. Over 54 genetic loci have been associated with obesity phenotypes and clinical studies are now reporting associations between SNPs and/or functional alterations of gene expression (epigenetics) and the ability to lose weight or not. We will implement a randomized clinical trial to test a set of genomic data called the FIT™ test (Pathway Genomics™) containing information on SNPs that affect obesity risk, confer specific diet recommendations, outline eating behaviors and suggest responses to various exercise regimens. The overall goal of this project is to evaluate if this supplemental genetic information with a genomically-derived diet built around packaged meals to improve adherence, in parallel with the MOVE! program at the VA in San Diego, will promote weight loss in more obese veterans than those receiving usual care and eating diets based around packaged meals. Our primary hypotheses are that more obese veterans in the MOVE! program will lose 5% of their weight if they receive personalized genomic information and a genomically-derived diet built around packaged meals when compared to veterans in the same program that receive usual care during MOVE! and packaged meals after 8 or 24 weeks. We also hypothesize that more veterans in the genomic group that lose 5% weight loss at 8 weeks will maintain this weight loss after 24 weeks compared to veterans in the usual care group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
Keywords
veteran, obesity, personalized genomics

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Usual Care
Arm Type
Placebo Comparator
Arm Description
Usual care for veterans as part of the MOVE! program
Arm Title
Personalized Genomics
Arm Type
Active Comparator
Arm Description
Personalized genomics information from the FIT Test, Pathway Genomics
Intervention Type
Genetic
Intervention Name(s)
Personalized Genomics
Other Intervention Name(s)
FIT test from Pathway Genomics, Inc.
Intervention Description
A set of single nucleotide polymorphisms in genes important for obesity, eating behaviors and exercise
Intervention Type
Genetic
Intervention Name(s)
Usual Care
Other Intervention Name(s)
Standard dietary recommendations
Intervention Description
Patients receive the same dietary recommendation regardless of their genetic information
Primary Outcome Measure Information:
Title
Number of Participants With Weight Loss of 5% or More at 8 Weeks
Description
Our primary hypotheses are that more obese veterans in the MOVE! program will lose greater or equal to 5% of their weight if they receive personalized genomic information and a genomically-derived diet built around packaged meals when compared to veterans in the same program that receive usual care during MOVE! and packaged meals after 8 weeks.
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Number of Participants With Weight Loss of 5% or More at 24 Weeks
Description
We hypothesize that more veterans in the genomic group that lose greater or equal to 5% weight loss at 8 weeks will maintain this weight loss after 24 weeks compared to veterans in the usual care group.
Time Frame
24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Veterans able to receive care at the VASDHS and planning to start the MOVE! program. Veterans able to understand and consent to the study. BMI equal to or greater than 30 kg/m2. Exclusion Criteria: Veterans unable to receive care at the VASDHS. Veterans unable to understand the consent process at the discretion of the PI. Active substance abuse or substance dependence disorder Cognitive disorder, psychiatric hospitalization in past 6-months, or presence of suicidal ideation identified on self-report instruments Bradycardia, rapid heart rate or other arrhythmia or active ischemia by EKG. Uncontrolled thyroid disease as measured by a TSH above or below the normal range. Body mass index < 30 kg/m2. Chronic kidney disease stage III or higher by National Kidney Foundation criteria (GFR = 30-59 ml/min). New York Heart Association's functional classification of congestive heart failure above Class I (not limited with normal physical activity by symptoms; Class II occurs when ordinary physical activity results in fatigue, dyspnea, or other symptoms). Sodium or potassium outside the normal range. Edema requiring the use of daily diuresis with furosemide, bumex or other diuretic (does not include hydrochlorthiazide). The use of high dose oral corticosteroids (above replacement doses). Veterans deficient in 25-OH vitamin D (<20 units/dl). Veterans with fasting LDL > 190 mg/dl. Veterans with fasting triglyceride levels > 1000 mg/dl. Excessive caffeine use (>6 caffeinated beverages/days). Prior gastrointestinal surgery with the exception of distal appendectomy. Acute infections or current use of antibiotic therapy.
Facility Information:
Facility Name
VA San Diego Healthcare System
City
San Diego
State/Province
California
ZIP/Postal Code
92161
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
25769412
Citation
Frankwich KA, Egnatios J, Kenyon ML, Rutledge TR, Liao PS, Gupta S, Herbst KL, Zarrinpar A. Differences in Weight Loss Between Persons on Standard Balanced vs Nutrigenetic Diets in a Randomized Controlled Trial. Clin Gastroenterol Hepatol. 2015 Sep;13(9):1625-1632.e1. doi: 10.1016/j.cgh.2015.02.044. Epub 2015 Mar 10.
Results Reference
derived

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Nutrigenomics: Personalizing Weight Loss for Obese Veterans

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