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Healthy Adult ParticipantsNCT07435831

Kimchi and Gut Health

A study testing 60 grams per day of intervention food in people with Healthy Adult Participants, run by University of California, Davis at 2 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The goal of this study is to learn about the effects of eating kimchi on the gut health of healthy adults in the USA. The investigators will be researching the changes in the gut microbiome, biomarkers of gut health and cardiometabolic health after consuming fermented and unfermented cabbage. Read more about this study

Who is it for?
Ages 19 to 70 yearsHealthy volunteers can take part
Conditions the study is for
Healthy Adult Participants
What is being tested?
60 grams per day of intervention food
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
2 sitesUnited States
Study dates
30 Mar 2026to Dec 2029
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 19 to 70 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • BMI of 25-30 kg/m2
  • No or occasional consumption of kimchi (3 or fewer times per week)
  • Willing to eat study food every day for 3 weeks
  • Willing to participate in study protocols

Who cannot join

  • Allergy to cabbage and /or cruciferous family vegetables
  • Allergy to kimchi ingredients such as shellfish and fish sauce
  • Daily consumption of kimchi
  • Diagnosed digestive issues such as irritable bowel syndrome (IBS) or gastrointestinal inflammatory bowel disease (IBD) or conditions such as Crohn's disease
  • Previous bowel surgery that disrupts the digestive flow, motility or gastric emptying process
  • Antibiotics used in the 2 months prior to enrollment
  • Unwillingness to discontinue probiotics during study and washout period
  • Active diagnosis and/or treatment for cancer

Trial locations and contacts

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

United States2 sites, 2 recruiting
  • Ragle Human Nutrition Center

    Davis, California, 95616

    Francene Steinberg, PhD, 530-752-0120, fmsteinberg@ucdavis.edu

    Recruiting
  • UC Davis Ragle Human Nutrition Research Center

    Davis, California, 95616

    Francene Steinberg, PhD, 530-752-0160, fmsteinberg@ucdavis.edu

    Jody Randolph, 5307527620, jmrandolph@ucdavis.edu

    Recruiting

Other trials in United States

About this study

Official title: Kimchi and Gut Health - Kimchi Effects on the Human Gut Microbiome

The goal of this study is to learn about the effects of eating kimchi on the gut health of healthy adults in the USA. The investigators will be researching the changes in the gut microbiome, biomarkers of gut health and cardiometabolic health after consuming fermented and unfermented cabbage.

The main questions it aims to answer are:

Read more

Does eating kimchi (fermented cabbage) result in enrichment of lactic acid bacteria in the stools of participants? Does eating kimchi result in metabolic changes in the gut microbiome, biomarkers of gut and cardiometabolic health of participants? Researchers will compare a group of participants eating fermented cabbage (kimchi) daily to a group of participants eating non-fermented cabbage daily.

Participants will:

Eat kimchi or cabbage daily for 3 weeks. Visit the study site for brief visits up to 5 times. Have blood drawn and provide a fecal sample 2 times - at beginning and end of the 3 week study.

Keep occasional records of food intake and questionnaires about any gastrointestinal symptoms that participants may have.

Being tested
60 grams per day of intervention food
Keywords
Healthy adult, GI health, Fermented food

What participants receive

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

  • 60 grams per day of intervention foodOther

    Non-fermented cabbage

  • 60 grams per day of intervention foodOther

    Kimchi fermented cabbage

Study groups in NCT07435831
Study groupRoleWhat they receive
KimchiExperimentalNot described
Receives: Other: 60 grams per day of intervention food
CabbageActive comparatorNot described
Receives: Other: 60 grams per day of intervention food

What is being measured

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

  1. Change from baseline in fecal Lactic Acid Bacteria (LAB)

    Measured: Baseline and week 3

Secondary outcomes (7)
  1. Fecal Metabolites - Change in short chain fatty acids (SCFA) and secondary bile acids (BA)

    Measured: Baseline and 3 weeks

  2. Gut integrity and health - Change in fecal calprotectin, fecal lipocalin, and fecal sIGA

    Measured: Baseline and 3 weeks

  3. Gut integrity and health - Change in plasma lipopolysaccharide binding protein (LBP), lipopolysaccharide (LPS), zonulin, and sCD14

    Measured: Baseline and 3 weeks

  4. Immune biomarkers - Change in plasma IL-6, TNF-alpha, hsCRP

    Measured: Baseline and 3 weeks

  5. Cardiometabolic biomarkers - Change in lipid panel (TC, LDL, HDL, TG), and oxidized LDL (oxLDL)

    Measured: Baseline and 3 weeks

  6. Qualitative self-assessment of gut associated health - Change in Gastrointestinal Symptom Rating Scale (GSRS)

    This questionnaire rates gastrointestinal symptoms over the past 7 days. A higher score indicates presence and increasing severity of symptoms and level of discomfort.

    Measured: Baseline and 3 weeks

  7. Qualitative self-assessment of gut associated health - Change in Digestion-associated Quality of Life Questionnaire (DQLQ)

    This questionnaire measures the effect of digestive symptoms on daily life over the past 7 days. A higher score indicates a lower (worse) digestion-associated Quality of Life.

    Measured: Baseline and 3 weeks

Timeline

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

  1. First posted27 Feb 2026
  2. Study start30 Mar 2026
  3. Primary completion30 Jan 2027 (estimated)
  4. Study completionDec 2029 (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
Single blind
Who is masked
Outcomes assessor
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07435831
Sponsor's protocol ID
2325615-1
Status last verified
Apr 2026
First submitted
22 Dec 2025
Last updated
2 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing 60 grams per day of intervention food in people with Healthy Adult Participants, run by University of California, Davis at 2 sites 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 4 inclusion and 8 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: looking for participants now, as of the sponsor's last update on 2 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites 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?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change from baseline in fecal Lactic Acid Bacteria (LAB) (time frame: Baseline and week 3). 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 2 Apr 2026.

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