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Healthy DietNCT05218980

Health-related Benefits of Introducing Table Olives Into the Diet of Young Adults: Olives For Health

A study testing Olives in people with Healthy Diet and Cholesterol, run by Yale University at 1 site in United States.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The purpose of this study is to assess whether introducing table olives into the diet results in health-related benefits for young adults. Several studies have shown that addition of olives as part of somebody's diet has a positive impact on cardiovascular, metabolic, and inflammatory factors. Read more about this study

Who is it for?
Ages 18 to 23 yearsHealthy volunteers can take part
Conditions the study is for
Healthy Diet, Cholesterol, Healthy Lifestyle
What is being tested?
Olives
Could I receive a placebo?
No, everyone receives an active treatment
How many people
226 participants
Where
1 siteUnited States
Study dates
Jan 2027to Jun 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 23 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Yale College Freshman, Sophomore, or Junior
  • Ability and desire to sign informed consent
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Male or female, age 18 on the day of consent
  • Ability and desire to consume 6 olives daily

Who cannot join

  • Yale College Senior
  • Unable to provide informed consent form
  • Self-reported pregnancy
  • Unwillingness to comply with all study procedures and/or be available for the duration of the study
  • Inability and desire to consistently consume 6 olives per day
  • Inability to consume fruit with pits
Show all 10Show fewer
  • Current and consistent use of > 6 olives per day
  • Current and consistent use of ≥ 1 tablespoon of extra virgin olive oil (EVOO) per day
  • Known allergic reactions to olives and/or their derivatives
  • Known reactions to blood draw

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Tassos Kyriakides, PhD contact

(203) 606-1401

tassos.kyriakides@yale.edu

United States1 site
  • Yale University

    New Haven, Connecticut, 06520

    Erica Rocco, BS, 203-785-4308, erica.rocco@yale.edu

Other trials in United States

About this study

The purpose of this study is to assess whether introducing table olives into the diet results in health-related benefits for young adults. Several studies have shown that addition of olives as part of somebody's diet has a positive impact on cardiovascular, metabolic, and inflammatory factors. However, there have not been many studies among young, healthy adults. This study will compare levels of specific biomarkers, collected through blood draw, at the beginning of the study and after 5 weeks, to evaluate the effects of investigational daily olive consumption.

Read the detailed description

This randomized clinical trial will intend to show compared to standard nutrition, nutrition that includes the daily consumption of 6 olives for 5 weeks will lead to a 4.5% decrease in the mean change (from baseline) in LDL. The primary objective of this study is to determine whether daily consumption of olives leads to clinically meaningful changes in metabolic and inflammatory biomarkers among adults 18-23 years old. The primary outcome is change in mean LDL. The secondary objective of this study is to evaluate the impact of daily consumption of olives on other biomarkers (HDL, LDL/HDL, HbA1c, CRP).

First, second- and third-year students (usually 18-23 years old) residing in the selected colleges will be informed about the study and following consent will be enrolled in the study if they meet the eligibility criteria. Prior to initiation of the project, the study team will present the study to the college student body over a series of presentations to be arranged with the assistance of the college leadership (Dean and Head of College). There has not been a lot of studies among young adults, who might not be at elevated risk for conditions related to nutrition. It is important to assess whether introduction of a food item that has shown benefit in other populations, would afford the same or higher benefit among this age group. Further, if the evidence generated from this study points to significant benefit, it might lead to changes in nutrition paradigms, both in the setting of college dining and/or outside, to incorporate olives.

A total of 226 participants will be enrolled, 113 in each of the two arms of the study. Study participants assigned to the intervention will consume 6 organic olives daily (individually packaged), provided at dinner times by Yale Dining Services. Assessment of receipt of the daily olives will be done at the time a participant wipes his/her card upon entry to the Dining facility at their college.

Selection of the residential colleges will be made following consultation and solicitation with the Heads of Yale Colleges, Dean of Yale College, and Yale Hospitality. Following identification of the Yale Colleges, several presentations to the college's student body will be made, to introduce and explain the project, and answer questions, expected to take place January-February 2021. Following such sessions, an email with the link to the study screening tool will be sent to the students by the college's administration. Interested students will be asked to complete a screening survey. Screening will also be available and accessible until the end of the study enrollment phase (February 11, 2022). At the beginning of the Spring 2022 semester, all students who have screened and are deemed eligible will be consented during the enrollment phase (February 7-11, 2022). Study personnel will be stationed outside the dining hall of the college during dinner hours, to e-consent the study participants using study iPads. Following consent, study personnel will collect the baseline and 5 week blood specimens from the study participant. At the end of the project, this data will be sent via secure data processes to the REDCap project location. Even though not anticipated given the nature of the intervention, adverse event (AEs) will be defined and collected as per standard definitions and severity assessment.

Being tested
Olives
Keywords
olives

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • OlivesDietary supplement

    Organic olives (provided by Sakellaropoulos Organic Farms; Sparta, Greece)

Study groups in NCT05218980
Study groupRoleWhat they receive
InvestigationalExperimentalYale Dining menu + 6 olives daily
Receives: Dietary Supplement: Olives
StandardNo interventionYale Dining menu only

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change From Baseline in Mean LDL at Week 5

    Blood draw to assess LDL at baseline and week five. Change will be calculated by comparing means of the differences (5 weeks-Baseline) between the two study groups, a decrease in the mean from baseline is positive.

    Measured: at baseline and week 5

  2. Compliance/adherence to daily intervention

    Assessment and verification of receipt of the olives will be tied to the dining hall card swipe that is part of the student's access to the dining facility, for study participants in the olives group. Swipe=adherent.

    Measured: up to week 5

Secondary outcomes (4)
  1. Change From Baseline in Mean HDL at Week 5

    Blood draw to assess HDL at baseline and week five. Change will be calculated by comparing means of the differences (5 weeks-Baseline) between the two study groups, a decrease in the mean from baseline is positive.

    Measured: at baseline and week 5

  2. Change From Baseline in Mean LDL/HDL at Week 5

    Blood draw to assess LDL/HDL ratio at baseline and week five. Change will be calculated by comparing means of the differences (5 weeks-Baseline) between the two study groups, a decrease in the mean from baseline is positive.

    Measured: at baseline and week 5

  3. Change From Baseline in Mean HbA1c at Week 5

    Blood draw to assess HbA1C at baseline and week five. Change will be calculated by comparing means of the differences (5 weeks-Baseline) between the two study groups, a decrease in the mean from baseline is positive.

    Measured: at baseline and week 5

  4. Change From Baseline in Mean CRP at Week 5

    Blood draw to assess CRP at baseline and week five. Change will be calculated by comparing means of the differences (5 weeks-Baseline) between the two study groups, a decrease in the mean from baseline is positive.

    Measured: at baseline and week 5

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Feb 2022
  2. Study startJan 2027 (estimated)
  3. Primary completionApr 2027 (estimated)
  4. Study completionJun 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
226 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05218980
Sponsor's protocol ID
2000031519
Other IDs
000
Status last verified
May 2026
First submitted
19 Jan 2022
Last updated
13 May 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Individual participant data that underlie the results reported in the primary publication; after deidentification (text, tables, figures and appendices)

Questions about this trial

What is this clinical trial studying?

A study testing Olives in people with Healthy Diet and Cholesterol, run by Yale University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 13 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Tassos Kyriakides, PhD ((203) 606-1401, tassos.kyriakides@yale.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change From Baseline in Mean LDL at Week 5 (time frame: at baseline and week 5). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 May 2026.

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