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Your smartwatch could predict blood sugar crashes before they happen

NCT ID NCT07633171

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Sep 18, 2026 · Updated 6 times

Summary

This study will test whether combining continuous glucose monitor (CGM) data with information from a smartwatch and a phone app (like meals and activity) can better predict blood sugar levels in people with type 2 diabetes. Thirty-six adults will wear a CGM and smartwatch and log their meals and exercise for several weeks. The goal is to build a model that gives real-time glucose predictions, but this study only collects data—it does not provide any treatment or recommendations.

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 lead to a smartphone app that predicts blood sugar changes in real time, helping people with type 2 diabetes manage their condition more easily.
What could go wrong
This is a small, early-stage study (36 people) that only collects data—it does not test a treatment. The model may not work well for everyone, and results may not apply to people outside this specific clinic.

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

About 36 people

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

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

Feb 2027

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.

Who is studied

Participants will be selected from the Johns Hopkins Medicine adult clinical population. The study population will include adults with type 2 diabetes who receive diabetes care through Johns Hopkins Medicine, including primary care and endocrinology clinics. Participants will be recruited from patients whose routine diabetes care includes use of continuous glucose monitoring and who may be eligible to contribute glucose, wearable, app-based behavioral, and electronic medical record data for development and validation of glucose prediction models.

Ages

18 to 75 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.

Inclusion Criteria: * 18-75 years old * Registered patient under Johns Hopkins Medicine (JHM) * Type 2 Diabetes diagnosis * Diabetes managed by a primary care physician or endocrinologist at JHM * Android Smartphone user * Must have a Dexcom G7 or FreeStyle Libre 3 CGM and using a mobile app to access their CGM data (G7 or Libre 3 apps) * 2 weeks of usage (with at least 50% wear time) prior to study participation required * CGM Time in Range of \<70% in 14 days prior to enrollment * Must be able to read, understand, and communicate in English * Must not have hearing or vision impairments * Willingness to Download the Welldoc app * Agree to wear a SAMSUNG Galaxy Watch at least 12 hours per day * Download SAMSUNG Health (Non-SAMSUNG Phone user) * Download Google Health Connect * Use CGM at least 80% of the time * Take a photo of all meals Exclusion Criteria: * Pregnant * Non-English speaker * Has hearing or vision impairment * Use of an insulin pump (i.e. automated insulin delivery system) * Diagnosed with other forms of diabetes (e.g. Type 1 Diabetes, Latent Autoimmune Diabetes in Adults (LADA), Maturity-Onset Diabetes of the Young (MODY), or Gestational diabetes) * Non-Android smartphone user (i.e., Apple iOS) * CGM time-below-range \> 4% (i.e. hypoglycemia) in the 14 days prior to enrollment. * Hospitalization for Diabetic Ketoacidosis (DKA) or severe hypoglycemic episode within the previous 6 months.

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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

    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.

    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

  • Johns Hopkins Medicine

    Baltimore, Maryland, 21287, United States

More trials for these conditions

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