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OpenTrials
Completed

NCT Number: NCT01859403

Nutrigenomics: Personalizing Weight Loss for Obese Veterans

This study aims to determine if providing genomic information to veterans can help them lose weight compared to usual care.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

VA San Diego Healthcare System

San Diego, California, 92161, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Personalized Genomics

Genetic

A set of single nucleotide polymorphisms in genes important for obesity, eating behaviors and exercise

Other names: FIT test from Pathway Genomics, Inc.

Usual Care

Genetic

Patients receive the same dietary recommendation regardless of their genetic information

Other names: Standard dietary recommendations

Primary outcomes

  1. Number of Participants With Weight Loss of 5% or More at 8 Weeks

    Time frame: 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 outcomes

  1. Number of Participants With Weight Loss of 5% or More at 24 Weeks

    Time frame: 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.

Sponsors and collaborators

Lead sponsor

University of California, San Diego

Other

Registry information

Important dates

Study start
2012
Primary completion
2013
Study completion
2014
First posted
May 21, 2013
Registry last updated
Apr 13, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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