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Nuts and Oil Pilot Study

A Feasibility Study of Tree Nut and Extra Virgin Olive Oil Supplementation to Improve Cardiometabolic Health

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04361617
Enrollment
34
Registered
2020-04-24
Start date
2021-07-19
Completion date
2022-04-20
Last updated
2023-09-18

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

Conditions

Metabolic Syndrome

Keywords

metabolic syndrome, extra virgin olive oil, tree nuts, DNA methylation

Brief summary

Metabolic syndrome is considered to be a state of prediabetes and is a major risk factor for cardiovascular disease. Dietary interventions involving extra virgin olive oil (EVOO) supplementation and tree nut consumption can improve cardiometabolic health and reverse metabolic syndrome. The goal of this exploratory study is to establish the feasibility of using a novel measure - epigenetic age - to motivate behavior change and improve cardiometabolic health in individuals with metabolic syndrome.

Detailed description

Metabolic syndrome (MetS) is a collection of at least three out of five cardiometabolic risk factors including abdominal obesity, hypertension, elevated blood glucose, hypertriglyceridemia, and low high-density lipoprotein cholesterol. MetS is a major risk factor for cardiovascular disease and is considered a state of prediabetes. Improving metabolic parameters through dietary, behavioral, and pharmacological interventions can improve or reverse MetS. For example, increased consumption of extra virgin olive oil (EVOO) and mixed nuts was shown to reduce cardiovascular event rates and reverse MetS in a 5-year study in Spain (PREDIMED study). However, lower levels of adherence to the PREDIMED intervention was found in participants with a higher number of cardiovascular risk factors, larger waist circumference, and lower physical activity levels at baseline. New strategies to convey one's risk of morbidity and mortality at the onset of a dietary intervention may improve intervention adherence, particularly among individuals meeting the criteria for MetS. A greater DNA methylation-based predicted age relative to chronological age, often referred to as epigenetic age acceleration, has been associated with many lifestyle factors, including physical activity and diet, as well as components of MetS, including obesity, blood pressure, HDL cholesterol and blood glucose levels. The investigators hypothesize that the majority of people with MetS have advanced epigenetic aging, and among those that have advanced epigenetic age, learning one's epigenetic age, and epigenetic age-based predicted risk of morbidity and mortality at the onset of a dietary intervention will improve participant adherence to the dietary intervention. Further, the investigators hypothesize that EVOO and tree nut supplementation in participants with MetS and advanced epigenetic age could help reverse MetS and potentially slow epigenetic aging. Therefore, the investigators plan to conduct a feasibility pilot study to: 1. To determine the proportion of participants with MetS with epigenetic age acceleration 2. To assess adherence to daily EVOO and tree nut consumption over a 4-week intervention in participants informed of epigenetic age acceleration at baseline compared to the control group 3. Qualitatively explore how participants perceive epigenetic age, and how participants' experiences would impact the feasibility of a larger clinical intervention in terms of challenges and motivators 4. Compare epigenetic age acceleration before and after the 4-week intervention For this study the investigators will recruit \ 50 individuals with MetS aged 35 years or older. An in-person assessment visit will be scheduled for a morning time and participants will be asked to be fasting and will be instructed to bring their medications to the visit. Candidates will review the informed consent document at an in-person screening with study staff prior to beginning their participation. For all participants providing informed consent, who were fasting and met the MetS criteria at the initial in-person assessment visit, collected blood samples will be used to calculate epigenetic age acceleration. Other measures to be collected include body weight, height, waist circumference, blood pressure, and questionnaires about demographics, health history and health habits. Participants that meet the inclusion criteria during the in-person screening visit will be contacted to schedule a baseline intervention visit. At the intervention visit, all participants will receive a 4-week supply of EVOO and tree nuts, including unsalted English walnuts, almonds or pistachios (approximately 10-day supply of each type). Participants will be asked to supplement their normal diets with these products and will be provided recipes and other information that will allow them to replace other foods with the nuts and oil. The investigators will ask participants to consume one ounce of tree nuts per day and two tablespoons of EVOO per day by incorporating these foods into their diet. Dietary adherence diaries will be given to measure incorporation of the study foods. Participants will be randomized to learn about epigenetic age acceleration (arm 1) or not to learn about epigenetic age acceleration (arm 2) in a 1:1 allocation at the baseline visit. Those in the intervention arm 1 that are to learn about epigenetic age acceleration will receive some educational materials and a brief description of epigenetic age acceleration. A telephone visit will be scheduled to take place at the end of week 1 for additional diet counseling, to assess safety/potential side effects and to collect adherence diaries. A follow-up phone call for compliance assessment and to answer participant questions will be conducted at the end of week 2. A final measurement visit will be scheduled for the end of week 4 for a morning time and participants will be asked to be fasting. At the final measurement visit, the same measures as listed in the in-person assessment visit will be performed and study questionnaires, with the exception of demographics and health history, will be distributed. After the intervention, participants will be asked to come in for the end of week 4 visit, For participants in the intervention arm 1 (participants educated about epigenetic age acceleration), a self- administered exit questionnaire will be given to qualitatively explore participants' perception of epigenetic age, and challenges and motivators for behavior change during the intervention, The open-ended questions will be designed to ascertain understanding of epigenetic age, and assess the challenges and motivators participants encounter during the intervention. Participants in both arms will be administered an Intervention Experience Assessment to explore how participant's experiences would impact the feasibility of a larger clinical intervention in terms of challenges and motivators. This feasibility study, incorporating epigenetic age estimates with a dietary intervention in individuals with MetS, is an initial step in building our understanding of 1) the relationship between MetS and epigenetic age, 2) how epigenetic age estimates may be perceived by patients at high risk for CVD, and 3) will provide preliminary longitudinal data examining the potential to slow epigenetic age acceleration predictions after a 4-week dietary intervention to provide feasibility for a larger future study.

Interventions

BEHAVIORALDaily consumption of tree nuts and extra virgin olive oil

All participants will receive a 4-week supply of extra virgin olive oil and tree nuts, including unsalted English walnuts, almonds or pistachios (approximately 3-day supply of each type). Participants will be asked to include in their normal diets these products and will be provided recipes and other information that will allow them to replace other foods with the nuts and oil. We will ask participants to consume one ounce of tree nuts per day and two tablespoons of EVOO per day by incorporating these foods into their diet.

Sponsors

National Center for Advancing Translational Sciences (NCATS)
CollaboratorNIH
Wake Forest University Health Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)

Masking description

Knowledge of intervention arm will not be given to research labs with samples

Eligibility

Sex/Gender
ALL
Age
35 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Men and Women ≥ 35 years of age * Metabolic syndrome, defined as \> 3 of the following: Waist circumference \>102 cm in men and \>88cm in women, triglycerides \>150 mg/dL and/or drug treatment for elevated triglycerides, HDL cholesterol \<40 mg/dL in men and \<50 mg/dL in women and/or drug treatment for reduced HDL cholesterol, systolic blood pressure \>130 mm Hg or diastolic blood pressure \>85 mmHg and/or antihypertensive drug treatment, and fasting glucose \>100 mg/dL or hemoglobin A1c \> 5.6% and/or oral hypoglycemic medications. * Willing to comply with study visits, as outlined in the protocol * Able to read and speak English * No allergies or hypersensitivities to olive oil or nuts * Ability to understand and the willingness to sign a written informed consent document.

Exclusion criteria

* Plans to move from the study area in the next 12 weeks * Body Mass Index (BMI) \> 40 kg/m2 * Dementia that is medically documented or suspected, or clinical evidence of cognitive impairment sufficient to impair protocol adherence * Candidate with any dietary practice, behavior or attitude that would substantially limit ability to adhere to protocol * Homebound for medical reasons * Living in the same household with another participant * Insulin-dependent Diabetes

Design outcomes

Primary

MeasureTime frameDescription
Proportion of Participants With MetS With Epigenetic Age AccelerationIn-person 1 day assessment visitTo characterize the relationship between MetS and epigenetic aging, we will examine epigenetic age acceleration prevalence among the 50 participants with metabolic syndrome.
Proportion of Days for Which EVOO Was Taken4 weeksAdherence for each participant will be measured as the proportion of days in 4 weeks for which EVOO was taken
Proportion of Days for Which Nuts Were Taken4 weeksAdherence for each participant will be measured as the proportion of days in 4 weeks for which nuts were taken
Proportion of Days for Which Nuts and EVOO Were Taken4 weeksAdherence for each participant will be measured as the proportion of days in 4 weeks for which both nuts and of EVOO were taken
Percentage of Participants Would be Able to Continue Eating the Tree Nuts and EVOO for a Study Like This Lasting 3-4 YearsAfter 4-week interventionQualitative interview with open-ended questions designed to ascertain participant understanding of epigenetic age, and assess the challenges and motivators participants encountered during the intervention. Will be assessed using qualitative analysis methods.

Secondary

MeasureTime frameDescription
Changes in Epigenetic Age AccelerationIn-person 1 day assessment visit vs. final 1 day visit after 4-week interventionThe investigators will compare epigenetic age acceleration before and after the 4-week intervention via DNA methylation test.DNA methylation profiles (beta-value, after adjustment chip and position effects) at 1,030 unique DNA methylation profiles will be used for epigenetic age acceleration predictions, using the DNA GrimAge predictor. The investigators will calculate predicted lifespan and regress predicted lifespan on chronological age to produce estimates of epigenetic age acceleration.

Countries

United States

Participant flow

Participants by arm

ArmCount
Epigenetic Age Knowledge Arm
Half of the intervention participants will be randomly selected to be informed of epigenetic age before the intervention. Daily consumption of tree nuts and extra virgin olive oil: All participants will receive a 4-week supply of extra virgin olive oil and tree nuts, including unsalted English walnuts, almonds or pistachios (approximately 3-day supply of each type). Participants will be asked to include in their normal diets these products and will be provided recipes and other information that will allow them to replace other foods with the nuts and oil. We will ask participants to consume one ounce of tree nuts per day and two tablespoons of EVOO per day by incorporating these foods into their diet.
17
No Epigenetic Age Knowledge Arm
The other half of intervention participants will not be informed of epigenetic age before the intervention. Daily consumption of tree nuts and extra virgin olive oil: All participants will receive a 4-week supply of extra virgin olive oil and tree nuts, including unsalted English walnuts, almonds or pistachios (approximately 3-day supply of each type). Participants will be asked to include in their normal diets these products and will be provided recipes and other information that will allow them to replace other foods with the nuts and oil. We will ask participants to consume one ounce of tree nuts per day and two tablespoons of EVOO per day by incorporating these foods into their diet.
17
Total34

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyWithdrawal by Subject01

Baseline characteristics

CharacteristicNo Epigenetic Age Knowledge ArmTotalEpigenetic Age Knowledge Arm
Age, Continuous70 years
STANDARD_DEVIATION 8
68 years
STANDARD_DEVIATION 10
65 years
STANDARD_DEVIATION 11
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
17 Participants34 Participants17 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
7 Participants13 Participants6 Participants
Race (NIH/OMB)
More than one race
1 Participants1 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
1 Participants1 Participants0 Participants
Race (NIH/OMB)
White
8 Participants19 Participants11 Participants
Sex: Female, Male
Female
8 Participants20 Participants12 Participants
Sex: Female, Male
Male
9 Participants14 Participants5 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 170 / 17
other
Total, other adverse events
2 / 173 / 17
serious
Total, serious adverse events
0 / 170 / 17

Outcome results

Primary

Percentage of Participants Would be Able to Continue Eating the Tree Nuts and EVOO for a Study Like This Lasting 3-4 Years

Qualitative interview with open-ended questions designed to ascertain participant understanding of epigenetic age, and assess the challenges and motivators participants encountered during the intervention. Will be assessed using qualitative analysis methods.

Time frame: After 4-week intervention

Population: % that would be able to continue eating the tree nuts and EVOO for a study like this lasting 3-4 years

ArmMeasureValue (NUMBER)
Epigenetic Age Knowledge ArmPercentage of Participants Would be Able to Continue Eating the Tree Nuts and EVOO for a Study Like This Lasting 3-4 Years76 Percentage of Participants
No Epigenetic Age Knowledge ArmPercentage of Participants Would be Able to Continue Eating the Tree Nuts and EVOO for a Study Like This Lasting 3-4 Years93 Percentage of Participants
Primary

Proportion of Days for Which EVOO Was Taken

Adherence for each participant will be measured as the proportion of days in 4 weeks for which EVOO was taken

Time frame: 4 weeks

Population: 3 samples failed DNAm QC analyses - 1 sample failed QC analyses

ArmMeasureValue (MEAN)Dispersion
Epigenetic Age Knowledge ArmProportion of Days for Which EVOO Was Taken0.96 proportion of daysStandard Deviation 0.08
No Epigenetic Age Knowledge ArmProportion of Days for Which EVOO Was Taken0.97 proportion of daysStandard Deviation 0.04
Primary

Proportion of Days for Which Nuts and EVOO Were Taken

Adherence for each participant will be measured as the proportion of days in 4 weeks for which both nuts and of EVOO were taken

Time frame: 4 weeks

Population: 3 samples failed to generate DNAm data passing QC analyses 1 sample failed to generate DNAm data passing QC analyses

ArmMeasureValue (MEAN)Dispersion
Epigenetic Age Knowledge ArmProportion of Days for Which Nuts and EVOO Were Taken0.948 proportion of daysStandard Deviation 0.076
No Epigenetic Age Knowledge ArmProportion of Days for Which Nuts and EVOO Were Taken0.967 proportion of daysStandard Deviation 0.041
Primary

Proportion of Days for Which Nuts Were Taken

Adherence for each participant will be measured as the proportion of days in 4 weeks for which nuts were taken

Time frame: 4 weeks

Population: 3 samples failed DNAm QC analyses - 1 sample failed QC analyses

ArmMeasureValue (MEAN)Dispersion
Epigenetic Age Knowledge ArmProportion of Days for Which Nuts Were Taken0.997 proportion of daysStandard Deviation 0.01
No Epigenetic Age Knowledge ArmProportion of Days for Which Nuts Were Taken0.997 proportion of daysStandard Deviation 0.041
Primary

Proportion of Participants With MetS With Epigenetic Age Acceleration

To characterize the relationship between MetS and epigenetic aging, we will examine epigenetic age acceleration prevalence among the 50 participants with metabolic syndrome.

Time frame: In-person 1 day assessment visit

Population: 3 samples failed DNAm QC analyses - 1 sample failed QC analyses

ArmMeasureValue (NUMBER)
Epigenetic Age Knowledge ArmProportion of Participants With MetS With Epigenetic Age Acceleration0.21 proportion of participants AgeAccelGrim>
No Epigenetic Age Knowledge ArmProportion of Participants With MetS With Epigenetic Age Acceleration0.53 proportion of participants AgeAccelGrim>
Secondary

Changes in Epigenetic Age Acceleration

The investigators will compare epigenetic age acceleration before and after the 4-week intervention via DNA methylation test.DNA methylation profiles (beta-value, after adjustment chip and position effects) at 1,030 unique DNA methylation profiles will be used for epigenetic age acceleration predictions, using the DNA GrimAge predictor. The investigators will calculate predicted lifespan and regress predicted lifespan on chronological age to produce estimates of epigenetic age acceleration.

Time frame: In-person 1 day assessment visit vs. final 1 day visit after 4-week intervention

Population: 3 samples failed to generate DNAm data passing QC analyses - 1 sample failed to generate DNAm data passing QC analyses

ArmMeasureValue (MEAN)Dispersion
Epigenetic Age Knowledge ArmChanges in Epigenetic Age Acceleration-0.2 AgeAccelGrim (years)Standard Deviation 1.4
No Epigenetic Age Knowledge ArmChanges in Epigenetic Age Acceleration0.1 AgeAccelGrim (years)Standard Deviation 1.3

Source: ClinicalTrials.gov · Data processed: Jul 31, 2026