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App aims to boost veggie intake with tailored feedback

NCT ID NCT07478068

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether a smartphone app that gives personalized recipes and feedback can help adults aged 18-45 who eat few vegetables increase their intake. 315 participants will log meals and some will get tailored advice. The goal is to see if digital tools can improve eating habits and engagement.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 315 people

The number the study aims to enrol. It can still change while the study runs.

Started

May 2025

Expected to finish

Mar 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 45 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Healthy males and females, age at start of the study ≥ 18 and ≤ 45 years; * Non-rejectors of Knorr (due to the recipes in the PDP application); * Currently cooking or intending to cook (\*themselves or partner) at least one main meal at home for at least five days a week; * Indicated desire to eat more vegetables; * In possession of an Android or iOS-based smartphone; * Willing to use an app to receive information and log all meals daily; * Currently using or willing to use a smartwatch; * Able to provide informed consent. Exclusion Criteria: * High reported baseline veg intake (participants need to self-report less than 50% of the UK rec / self-reported intake above the UK adult average (206 g/2.6 servings)); * Reported participation in another nutritional or biomedical trial within 1 month before the screening or during the study; * Planned frequent travel (\>2/month) and travel to countries with time zone \>GMT +04:00 during the study period; * Habitual consumption of \>14 units (female participants) and \>21 units (male participants) alcoholic drinks in a typical week; * Reported start or change in use of any nicotine containing products directly preceding the study or during the study itself; * If female, is pregnant (or has been pregnant during the last \<3 months) or will be planning pregnancy during the study period; * If female, is lactating or has been lactating in the 6 weeks before screening and/or during the study period; * Reported dietary habits: medically prescribed diet, slimming diet, any condition or self-prescribed diet that restricts consumption of vegetables, not used to eating at least 3 meals a day; * Reported body mass loss/gain (\>5%) in the last 3 months before the study. Self-reported history of major depressive disorders and/or current use antidepressive/antianxiety medication; * Clinically diagnosed sleep disorders and/or use prescribed sleep medication. Taking medication (including traditional medicines and or dietary supplements) which may pose undue personal risk or introduce bias into study measurements, as judged by the PI; * An allergy to adhesives, which would prevent proper attachment of the CGM; * Being an employee of any company developing personalised diet applications, including Salus Optima or Unilever.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

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  3. A doctor treating you

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Contacts and locations

Locations

  • Univeristy of Bath

    RECRUITING

    Bath, Somerset, BA2 7AY, United Kingdom