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Sweet taste test may reveal hidden clues about mental health

NCT ID NCT06697847

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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)

Expanded access
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
The full record has not been published yet, so there is little to show here.
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This status has not been confirmed recently, so it may be out of date.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 explores whether the ability to detect sweetness is linked to mood in healthy adults. Researchers will measure the lowest concentration of sugar water that participants can taste and compare it with scores on a standard mood questionnaire. The goal is to better understand how taste perception might relate to mental health, potentially paving the way for new screening approaches.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could help identify taste-based markers for mood disorders, potentially leading to earlier detection or new screening tools.
What could go wrong
This is a small, early-stage observational study in healthy volunteers, so results may not apply to people with mood disorders. It is exploratory and not designed to test a treatment.

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.

Participants

30 people

The number who actually took part.

Started

Nov 2024

Finished

Mar 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

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

Who is studied

Adults without mood questionnaires recruited by word of mouth and posters in retail establishments in England and Wales

Ages

18 years and older

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: . Male and female adults of 18 years old and over; * Participants without a diagnosis of major depressive disorder (MDD) / anxiety disorder; * Participants not taking an antidepressant during the preceding 6 months * Not suffering from significant other mental or physical illness, such as confirmed psychosis, end of life care, or any other condition assessed as significant by the Site Investigator; * Willing and able to comply with all study-related procedures; * Not having COVID 19 or continuing effects of COVID 19 including altered sense of taste; * Understands the study requirements and the treatment procedures and is able to provide written informed consent. Exclusion Criteria: * Taking antidepressant medication currently or during the previous 6 months; * Known or suspected hypersensitivity or intolerance to any taste testing solutions, or any of their excipients; * A history or presence of neurological or confounding psychiatric conditions (such as stroke, traumatic brain injury, epilepsy, space occupying lesions, multiple sclerosis, Parkinson's disease, vascular dementia, transient ischemic attack, or schizophrenia); * Patients with a diagnosis of chronic pain; * Pregnancy or possibility pregnancy, or breastfeeding; * Participants using supplements containing psychoactive herbs (for example St Johns Wort or 5-HTP (5-Hydroxytryptophan, also known as oxitriptan); * Participants regularly using psychoactive stimulants (for example MDMA); * Participants unable or unwilling to comply with study procedures.

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Westbury Lodge, Westbury Park

    Bristol, City Of Bristol, BS6 7JE, United Kingdom