Skip to content

Greens-Based Crossover Trial to Improve Epigenetic Aging in Adults

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

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06537232
Enrollment
20
Registered
2024-08-05
Start date
2024-09-04
Completion date
2025-03-31
Last updated
2025-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging

Keywords

Epigenetic aging, Microbiome, Quality of Life, Overweight and Obesity

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.

Interventions

DIETARY_SUPPLEMENTGreens-based Supplement

Participant will consume one serving of greens-based supplement per day in the morning, for 30 days.

Sponsors

Brickhouse Nutrition
CollaboratorUNKNOWN
Auburn University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE

Intervention model description

Randomized crossover trial

Eligibility

Sex/Gender
ALL
Age
50 Years to 65 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Changes in DNA Methylation in Peripheral Blood Mononuclear CellsChange 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

MeasureTime frameDescription
Fasting serum low-density lipoproteins (LDL)Change from day 0 (baseline) to day 30 post intervention supplementation.Phlebotomy will be obtained while fasted 8+ hours and low-density lipoproteins (LDL) will be measured as part of a comprehensive metabolic panel and reported in mg/dl. Lower concentrations are optimal.
Fasting serum blood glucoseChange from day 0 (baseline) to day 30 post intervention supplementation.Phlebotomy will be obtained while fasted 8+ hours and blood glucose will be measured as part of a comprehensive metabolic panel and reported in mg/dl. Lower concentrations are optimal.
Visceral fat percentageChange from Day 0 (baseline), Day 30 (Crossover/Midpoint ), and Day 60 (end of study)Change in visceral fat as a percentage of total fat mass as measured by bioelectrical impedance (BIA). Lower values are optimal.
Total body fat percentageChange from Day 0 (baseline), Day 30 (Crossover/Midpoint ), and Day 60 (end of study)Change in total body fat as a percentage of total fat mass as measured by bioelectrical impedance (BIA). Lower values are optimal.
Stool microbiome compositionChange from Day 0 (baseline), Day 30 (Crossover/Midpoint ), and Day 60 (end of study)16S changes in microbiome alpha diversity.
Fasting serum triglyceridesChange from day 0 (baseline) to day 30 post intervention supplementation.Phlebotomy will be obtained while fasted 8+ hours and triglycerides will be measured as part of a comprehensive metabolic panel and reported in mg/dl. Lower concentrations are optimal.
Breath Methane (ppm)Change from Day 0 (baseline), Day 30 (Crossover/Midpoint ), and Day 60 (end of study)Breath methane will be measured via QuinTron BreathTracker SC Analyzer every 30minutes to 1.5 hours on days 21 and 51. Lower levels are optimal.
Physical Quality of LifeChange from Baseline (day 0), Crossover/Midpoint (day 30), and End of study (day 60)The SF-12 PCS (Short Form-12, Physical Component Score) is a health-related quality of life measure that assesses general physical functioning and well-being. SF-12 PCS scores range from 0-100 with higher scores indicating better general physical health.
Sleep and Physical Activity- accelerometryChange from Baseline (day 0), Crossover/Midpoint (day 30), and End of study (day 60)Average minutes of total daily sleep and physical activity measured via garmin watch.
Total caloric intakeChange from Baseline (day 0), Crossover/Midpoint (day 30), and End of study (day 60)Three 24-hour dietary recalls will be obtained and entered into the and analyzed in the Nutrition Data System for Research (NDSR).
Mental Quality of LifeChange from Baseline (day 0), Crossover/Midpoint (day 30), and End of study (day 60)The SF-12 MCS (Short Form-12, Mental Component Score) is a health-related quality of life measure that assesses general mental health status. SF-12 MCS scores range from 0-100 with higher scores indicating better general mental health.
Breath Hydrogen (ppm)Change from Day 0 (baseline), Day 30 (Crossover/Midpoint ), and Day 60 (end of study)Breath hydrogen will be measured via QuinTron BreathTracker SC Analyzer every 30 minutes to 1.5 hours on days 21 and 51. Lower levels are optimal.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026