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HealthyBARITONENCT07128940

Biomarker pAtterns Reflecting habITual fOod iNtakE: the BARITONE Project

A study testing Meat vs fish, Meat vs Vegetarian and Fish vs Vegetarian in people with Healthy, run by Göteborg University at 1 site in Sweden.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The BARITONE study's overall aim is to understand how our eating habits affect our long-term health. By identifying biological traces in blood, urine and other samples - so-called biomarkers - the investigators want to be able to see what people actually eat, such as protein from different food sources as well as… Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Healthy
What is being tested?
Meat vs fish, Meat vs Vegetarian and Fish vs Vegetarian
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteSweden
Study dates
15 Sep 2025to 31 Mar 2026
Phase
Interventional
Are there results?
None posted in the registry

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 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Healthy adult
  • 18-65 years
  • BMI 18.5-30 kg/m²
  • Willing to consume the three diets i.e. meat, fish, and vegetarian
  • Understands Swedish
  • Low intake of vegetables, fruit and berries (lowest tertile of screened participants, estimated <100g day) or high intake of vegetables, fruit and berries (highest tertile of screened participants, estimated >400g day)

Who cannot join

  • Pregnancy and lactation
  • Diagnosis of cancer or other life threatening diseases
  • Diagnosis of metabolic or food related diseases inluding diabetes, inflammatory bowel disease, hypothyroidism or celiak disease.
  • Medication that influences the metabolism such as blood lipid lowering medication, insulin, etc.
  • Use of drugs other than medication and alcohol
  • Nicotine use (snuff, vaping and smoking)

Trial locations and contacts

1 site in 1 country.

Sweden1 site
  • University of Gothenburg

    Gothenburg, 405 30

Other trials in Sweden

About this study

The BARITONE study's overall aim is to understand how our eating habits affect our long-term health. By identifying biological traces in blood, urine and other samples - so-called biomarkers - the investigators want to be able to see what people actually eat, such as protein from different food sources as well as fruit, berries and vegetables. These biomarkers could in the future improve the possibilities to find out how dietary habits affect the risk of disease.

The investigators are targeting healthy people who are interested in participating in research on biomarkers of dietary intake. The research is divided into a cross-sectional study, where the investigators collect data on the participant's usual dietary intake, health and biological samples at the screening visit, and an cross over intervention study that involves eating three different diets (meat, fish, vegetarian) for a total of 3 weeks with one week wash-out in between.

Read the detailed description

PURPOSE AND AIMS

The aims of the present project are to:

  1. Identify and validate biomarker patterns of intake of the different food sources for protein, i.e., meat, fish and plant-based sources
  2. Identify and validate biomarker patterns of high and low intake of the food group vegetables, fruit and berries.

Validation here includes evaluation of plausibility, robustness, and dose-response.

PROJECT DESCRIPTION Validated biomarkers are still lacking for food groups that are crucial when evaluating dietary intake, such as meat, fish and plant-based sources of protein (i.e., legumes such as lentils, peas and beans and cereal proteins such as oat- and wheat-protein); and for berries, fruits, and vegetables. For sources of protein, a well-controlled cross-over trial is needed where biomarkers of any intake of these different sources are evaluated in different biofluids. For berries, fruit and vegetables, a challenge is that no obvious control food group exists. Individuals with low consumption from this food group may instead consume any type of food. Hence, the investigators aim to evaluate biomarkers that separate consumers of low vs high intake. The investigators will follow the criteria for discovering and validating biomarkers suggested by Dragstedt et al (2018), here applied to patterns of biomarkers. The investigators will identify patterns of putative biomarkers of recent intake in biofluids in a well-controlled feeding trial (BARITONE-intervention) and develop prediction models of being a consumer/non-consumer or high/low consumer using machine learning. The robustness and dose-response of the models will be tested in data on habitual intake (BARITONE sample). Data for protein sources and berries, fruits and vegetables will be generated in the planned BARITONE-intervention trial.

Biomarker pAtterns Reflecting habITual fOod iNtakE: the BARITONE project The BARITONE project consists of two parts: 1) the BARITONE-sample (n=210) that undergoes a comprehensive baseline screening with extensive phenotyping including a 7-day weighed food diary (wk 1), and 2) the BARITONE cross-over intervention trial (n=70) where a selected group from the BARITONE-sample undergoes three dietary intervention weeks with two 7-day weighed food diaries during the two washout weeks in between.

The BARITONE-sample will be used to evaluate robustness and dose-response of putative biomarker patterns of habitual intake, because it will contain highly detailed data on habitual dietary intake and individual phenotype/metabotype. The intervention weeks of the BARITONE-trial will be used to identify putative biomarker patterns of recent intake of protein sources. Because it is a cross-over trial it allows for within-individual comparisons on metabolite reactions to dietary exposure. The wash-out periods between intervention weeks will be used to identify putative biomarker patterns of recent high or low intake of berries, fruits and vegetables, because participants will be selected based on baseline intake levels of these foods and here asked to return to their habitual diet. Hence, broad variation in intake should be represented.

The BARITONE sample for habitual diet In total, 210 healthy individuals aged 18-65 years will be invited through advertisements in media to detailed phenotyping at the laboratory of Clinical Nutrition, Gothenburg University. Procedures include a socio-demographic and lifestyle questionnaire (chronic illnesses, pharmacological treatment, physical activity, questions about menopause/timing in the menstrual cycle), a short food frequency questionnaire (FFQ), a 7-day weighed food diary and measurements of anthropometry (weight, height, body mass index, body composition by dual energy X-ray absorptiometry (DXA) or bioelectrical impedance analysis (BIA)). Biospecimens (fasting blood, spot urine; baseline stool samples) will be collected and analyzed for serum lipids, Hb, HbA1c, TSH, metabolomics including lipidomics and baseline gut microbiota.

The BARITONE cross-over intervention trial for recent intake of protein sources (Aim 1)

The BARITONE trial aims to identify metabolite patterns that can separate individuals with respect to intake of meat, fish or plant-based source of protein. From the BARITONE -sample, the investigators will select 35 participants with low intake of berries, fruit and vegetables and 35 with high intake of these same foods, to ensure a wide range of habitual intake of these foods to address Aim 2. Selection will be based on their baseline FFQ. The limit for low (<100g/day) and high intake (>400g/day) are based on the 15:th and 85:th percentile of intake data on vegetables, fruit and berries, from Riksmaten. Participants will be randomized by excel randomization function to order of trial diets by an external researcher. Blinding of participants is not possible in this diet intervention.

Intervention week diets: The diets will be identical in foods and macronutrient composition except for meat, fish or plant-based source of protein. Participants will be provided with all their food for the three trial weeks, with one week wash-out periods between the intervention periods when habitual consumption patterns should resume. Food bags will be delivered free of charge at the day before each intervention week including instructions, recipes and menus. Water will be the suggested drink. Non-sweetened drinks, coffee and tea will not be provided, but participants are allowed to consume these freely and report the intake and they should keep the consumption constant during all three intervention weeks. Alcohol will not be allowed during the intervention weeks.

The BARITONE wash-out weeks for habitual intake of berries, fruits, and vegetables (Aim 2): Detailed 7-days weighed food diaries will be collected during the two wash-out weeks among the trial participants, already selected to have low or high habitual intake of berries, fruits and vegetables. The diaries will be used to verify classification of the participants into high and low consumers. Metabolite patterns in the biofluids collected at the end of each wash-out period will be used to construct models for predicting intake of berries, fruit and vegetables, and thereafter robustness of the models will be evaluated in the BARITONE-sample.

Conditions
Healthy
Being tested
Meat vs fish, Meat vs Vegetarian, Fish vs Vegetarian
Keywords
food, biomarker, metabolomics, fruit and vegetables, meat, fish, plant based protein, whole grain

What participants receive

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

  • Meat vs fishOther

    Metabolite differences: Meat vs fish

  • Meat vs VegetarianOther

    Metabolite differences: Meat vs Vegetarian

  • Fish vs VegetarianOther

    Metabolite differences: Fish vs Vegetarian

Study groups in NCT07128940
Study groupRoleWhat they receive
MeatExperimentalAll food provided for a week, including a variety of meat
Receives: Other: Meat vs fish; Other: Meat vs Vegetarian
FishExperimentalAll food provided for a week, including a variety of fish and shellfish
Receives: Other: Meat vs fish; Other: Fish vs Vegetarian
VegetarianExperimentalAll food provided for a week, diet (no fish or meat)
Receives: Other: Meat vs Vegetarian; Other: Fish vs Vegetarian

What is being measured

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

  1. Patterns of metabolites in plasma/serum

    Metabolites analysed by LC-MS/GC-MS or NMR for metabolomics studies (changes in patterns of metabolites). Metabolite patterns will be compared by multivariate methods such as HDA-OPLS between the three diets. Metabolite patterns will be compared by multivariate methods such as OPLS-DA comparing high and low intake of vegetables, fruit and berries.

    Measured: 1 week

Secondary outcomes (3)
  1. Patterns of lipids

    Lipids analysed by lipidomics. Changes in lipidomic patterns will be compared by multivariate methods such as HDA-OPLS between the three diets. Lipidomics patterns will be compared by multivariate methods such as OPLS-DA comparing high and low intake of vegetables, fruit and berries.

    Measured: 1 week

  2. Patterns of metabolites in urine

    Metabolites analysed by LC-MS/GC-MS or NMR for metabolomics studies (changes in patterns of metabolites). Metabolite patterns will be compared by multivariate methods such as HDA-OPLS between the three diets. Metabolite patterns will be compared by multivariate methods such as OPLS-DA comparing high and low intake of vegetables, fruit and berries.

    Measured: 1 week

  3. Class disciminating metabolites in plasma/serum

    Among the thousands of metabolites analysed by LC-MS/GC-MS or NMR for metabolomics studies a few metabolites may drive the metabolite patterns. These class discriminating metabolites (our limit is the 20 highest top-ranked variables in variable importance scores in the OPLS-HDA models) will be selected and further analysed by univariate methods.

    Measured: 1 week

Timeline

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

  1. First posted19 Aug 2025
  2. Study start15 Sep 2025
  3. Primary completion31 Mar 2026
  4. Study completion31 Mar 2026

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
Other
Allocation
Randomised
Intervention model
Crossover
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
100 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07128940
Sponsor's protocol ID
BARITONE
Acronym
BARITONE
Status last verified
Feb 2026
First submitted
26 Jun 2025
Last updated
22 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Not possible due to Swedish law

Questions about this trial

What is this clinical trial studying?

A study testing Meat vs fish, Meat vs Vegetarian and Fish vs Vegetarian in people with Healthy, run by Göteborg University at 1 site in Sweden.

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 6 inclusion and 6 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: finished, as of the sponsor's last update on 22 Jun 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 Sweden. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Patterns of metabolites in plasma/serum (time frame: 1 week). 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 22 Jun 2026.

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