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N/A Completed N=51 Randomized Treatment

Nutrigenomics: Personalizing Weight Loss for Obese Veterans

Source: ClinicalTrials.gov NCT01859403 ↗
Enrolled (actual)
51
Serious AEs
0.0%
Results posted
Mar 2021
Primary outcomePrimary: Number of Participants With Weight Loss of 5% or More at 8 Weeks — 7; 7 Participants

Summary

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

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Weight Loss of 5% or More at 8 Weeks
7; 7
SECONDARY
Number of Participants With Weight Loss of 5% or More at 24 Weeks
5; 7

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 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.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01859403). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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