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Soya drink shows promise for weight loss in overweight adults

NCT ID NCT07614178

Disease control Sponsor: Universiti Sains Malaysia Source: ClinicalTrials.gov ↗

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested whether a soya-based dietary fiber drink could help overweight adults lose weight and improve their health. Over 12 weeks, 42 participants either drank the soya beverage or continued their normal diet. Researchers measured changes in weight, body fat, and other health markers to see if the drink made a difference.

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

42 people

The number who actually took part.

Started

Jun 2025

Finished

Dec 2025

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 50 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: * Staff or students aged 18-50 years * Participants with BMI 23-30 kg/m2 * Participants physically inactive * Not having any allergies to any of the known food ingredients, especially milk and soy * Not on lipid-lowering and oral hypoglycemic drugs * No kidney diseases Exclusion Criteria: * Pregnant or lactating mothers * Having known chronic disease conditions * Having a known allergy history for soy and milk or any of the ingredients in the formula. * History of any type of minor or major surgical procedure in the past 6 months. * Currently on diet prescriptions or participating in regular physical activity sessions. * On weight loss drugs or consuming dietary supplements such as protein shakes, whey protein, casein, fruit juices or fiber-based supplements.

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Conditions

The condition(s) this trial relates to.

Overweight Weight Loss

As listed by the trial registrant

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

Overweight adults

Contacts and locations

Locations

  • Health Campus, Universiti Sains Malaysia

    Kubang Kerian, Kelantan, 16150, Malaysia

More trials for these conditions

Other studies related to the condition(s) this trial covers.