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Tiny sensor could help millions avoid diabetes

NCT ID NCT07371546

What the study statuses mean

This study's is highlighted.

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 Results may not be published yet.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)

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This status has not been confirmed recently, so it may be out of date.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 tests whether wearing a continuous glucose monitor (CGM) helps adults with prediabetes improve their diet and physical activity compared to standard health coaching. 76 participants from a Singapore polyclinic will be randomly assigned to receive either a CGM plus coaching or coaching alone. The study also interviews patients and healthcare providers to understand the real-world benefits and challenges of using CGM for prediabetes.

What this could mean

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

Active substance
Continuous glucose monitor (Abbott Freestyle Libre)
What this could lead to
If successful, this could show that CGM helps people with prediabetes make healthier choices and lower their risk of developing type 2 diabetes.
What could go wrong
This is a small, early-stage study (76 participants) focused on feasibility and behavior, not on preventing diabetes. Results may not apply to larger populations.

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 76 people

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

Started

Oct 2025

Expected to finish

Dec 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

21 to 69 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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.

Patient Participants Inclusion Criteria: 1. Singaporean Citizen or Permanent Resident 2. Age 21 - 69 years old 3. Clinical diagnosis of prediabetes defined as a fasting glucose of 6.1-6.9 mmol/L and/or 2-hour glucose level of 7.8-11.0 mmol/L after an oral glucose tolerance test (Appropriate Care Guide, 2021) a. Can be conservatively managed, or medically managed with metformin 4. Owns a mobile phone that can download the Singapore FreeStyle LibreLink App 5. Expressed willingness to use participate in the study, use the devices according to the study protocol during the study period, and to sign informed consent. Exclusion Criteria: 1. Pregnant or planned pregnancy within the next six months 2. Physical limitation that prevents the patient from engaging in physical exercise 3. Cognitively impaired based on diagnosis of dementia or mild cognitive impairment (MCI) in the electronic health records (EHR) 4. Not adequately proficient in English 5. Currently enrolled in another study or program that involves weight loss or dietary modifications, or novel therapeutic drug or device 6. Planned surgery in the next six months 7. Not able to use smartphone or the Singapore FreeStyle LibreLink App despite coaching 8. Any end-stage disease with life prognosis of \< 2 years 9. Patients who are not willing or are not able to commit to the entire study program Healthcare Providers (HCP) Participants HCPs from Pasir Ris Polyclinic who self-reported to have treated adults with prediabetes will be enrolled for the interviews.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. 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.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Pasir Ris Polyclinic

    RECRUITING

    Singapore, 519466, Singapore

  • Pasir Ris Polyclinic

    RECRUITING

    Singapore, Singapore

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