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Clinical Trials/NCT06537232
NCT06537232
Active, Not Recruiting
N/A

A Randomized Crossover-Controlled Trial Investigating the Epigenetic Impact of a Greens-Based Supplement in Adults

Auburn University1 site in 1 country20 target enrollmentSeptember 4, 2024
ConditionsAging

Overview

Phase
N/A
Intervention
Not specified
Conditions
Aging
Sponsor
Auburn University
Enrollment
20
Locations
1
Primary Endpoint
Changes in DNA Methylation in Peripheral Blood Mononuclear Cells
Status
Active, Not Recruiting
Last Updated
last year

Overview

Brief Summary

The primary purpose of this study is to assess changes in epigenetic markers of aging and physiological parameters in overweight older adults consuming a mixed greens-based supplement over a 30-day period in a randomized crossover design.

Detailed Description

Investigators will recruit 20 overweight/obese but otherwise healthy participants aged 50-65. Participants will be randomized to consume the greens-based supplement each morning for the first 30 days or second 30 days of the study. Usual diet, physical activity, and sleep patterns will be encouraged and monitored during the duration of the study. Phlebotomy will be conducted at baseline, 30-day crossover, and 60-day follow-up to assess DNA methylation in peripheral blood mononuclear cells. Visceral and total body fat, stool microbiome composition, and actigraphy will also be assessed.

Registry
clinicaltrials.gov
Start Date
September 4, 2024
End Date
March 2025
Last Updated
last year
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Andrew Fruge

Associate Professor

Auburn University

Eligibility Criteria

Inclusion Criteria

  • Men and women of any ethnicity (women must be postmenopausal)
  • Body Mass Index \> 30 kg/m\^2
  • Low habitual dark green leafy vegetable consumption
  • Willing to adhere to study protocol and measures
  • Willing to communicate via smartphone technology
  • Able to read, write and speak English

Exclusion Criteria

  • Overt cardiometabolic diseases such heart attack, stroke, diabetes, insulin resistance and non-alcoholic fatty liver disease, etc.
  • Diagnosis of a transient ischemic attack in the 6 months prior to screening
  • Diagnosis of cancer within 5 years prior to screening, except for cutaneous basal cell or squamous cell cancer resolved by excision
  • Food allergies

Outcomes

Primary Outcomes

Changes in DNA Methylation in Peripheral Blood Mononuclear Cells

Time Frame: Change from day 0 (baseline) to day 30 post intervention supplementation.

Change from Baseline in Epigenetic Aging Profiles (i.e. DNA Methylation), after 30 day intervention. Participants will provide blood samples at their baseline study visit, which occurs before the start of the intervention, and at their visit at the end of the 30th of intervention supplementation.

Secondary Outcomes

  • Fasting serum triglycerides(Change from day 0 (baseline) to day 30 post intervention supplementation.)
  • Fasting serum low-density lipoproteins (LDL)(Change from day 0 (baseline) to day 30 post intervention supplementation.)
  • Fasting serum blood glucose(Change from day 0 (baseline) to day 30 post intervention supplementation.)
  • Visceral fat percentage(Change from Day 0 (baseline), Day 30 (Crossover/Midpoint ), and Day 60 (end of study))
  • Total body fat percentage(Change from Day 0 (baseline), Day 30 (Crossover/Midpoint ), and Day 60 (end of study))
  • Stool microbiome composition(Change from Day 0 (baseline), Day 30 (Crossover/Midpoint ), and Day 60 (end of study))
  • Breath Hydrogen (ppm)(Change from Day 0 (baseline), Day 30 (Crossover/Midpoint ), and Day 60 (end of study))
  • Breath Methane (ppm)(Change from Day 0 (baseline), Day 30 (Crossover/Midpoint ), and Day 60 (end of study))
  • Physical Quality of Life(Change from Baseline (day 0), Crossover/Midpoint (day 30), and End of study (day 60))
  • Sleep and Physical Activity- accelerometry(Change from Baseline (day 0), Crossover/Midpoint (day 30), and End of study (day 60))
  • Total caloric intake(Change from Baseline (day 0), Crossover/Midpoint (day 30), and End of study (day 60))
  • Mental Quality of Life(Change from Baseline (day 0), Crossover/Midpoint (day 30), and End of study (day 60))

Study Sites (1)

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