CClinicalTrials.gg
RecruitingNCT07373418GlowUpUpdated Jan 28, 2026

Glucose Observation and Wearable Use for Prevention

An observational study in Prevention, sponsored by University of St.Gallen. Recruiting at 1 site in Switzerland. Open to participants aged 45 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-28.

Sponsored by University of St.Gallen · Observational

From the registry’s dates

  • Started Dec 2025; still recruiting 9 months later.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
200
Ages
45 Years and older
Sex
All
01

Study summary

The GLOW UP study is a single-center, prospective, observational case-control study conducted in St. Gallen, Switzerland. The primary aim of the study is to examine to what degree lifestyle data collected from wearable devices and a smartphone app can identify individuals with prediabetes (vs. normoglycemic) in a real-world setting. The study also aims to characterize variability in lifestyle and glycemic patterns and to examine how between- and within-person differences relate to diabetes risk; to identify personalized predictors of early metabolic dysregulation. The study also evaluates new image-based meal tracking algorithms for predicting glycemic control and examines how reminder messages influence adherence to a \~4-week meal logging protocol.

The study aims to enroll 200 adults aged 45 years and older with a BMI of at least 25 kg/m² and no known diagnosis of diabetes, including 100 participants with prediabetes and 100 normoglycemic (metabolically healthy) controls. Participants will be classified at the baseline visit using HbA1c and fasting plasma glucose (FPG) tests, with prediabetes defined as HbA1c 5.7-6.4% and/or FPG 5.6-6.9 mmol/L, and normoglycemia defined as HbA1c \<5.7% and FPG \<5.6 mmol/L, following clinical standards. During the \~4-week observational period, participants will be asked to wear a smart ring, a wrist-worn smartwatch, and a blinded continuous glucose monitor (CGM). Participants will be asked to log/take-images of their meals via a study app and to complete brief questionnaires (e.g., tracking mood, stress, and contextual meal annotations) via ecological momentary assessments. FPG and HbA1c samples will be collected at baseline to classify participants as prediabetic or normoglycemic, and again at follow-up (\~4 weeks), which will serve as the primary outcome to evaluate associations between lifestyle and wearable-derived data and diabetes risk status.

02

Conditions studied

  • Prevention
03

In context

Lead sponsor

University of St.Gallen is the lead sponsor of 5 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
45 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Adults ≥45 years with BMI ≥25 kg/m², German-speaking residents of Switzerland, without known diabetes, recruited from GP practices, community and workplace channels, and general public advertisements.

Inclusion criteria

  • Citizens or residents of Switzerland who are German-speaking (main place of living or employment in Switzerland).
  • Age ≥45 years.
  • BMI ≥25 kg/m² (overweight or obese).
  • Regular access to a smartphone (iOS or Android) with a data plan.
  • Able to use smartphone applications.
  • Able to walk independently.

Exclusion criteria

Exclusion Criteria:

  • History of stroke, heart disease, renal failure, cancer, or diabetes (type 1 or type 2).
  • Past vascular bypass surgery or angioplasty.
  • Current or planned use of glucose-lowering medications during the upcoming 4 weeks (e.g., GLP-1 receptor agonists, metformin).
  • Pregnant or breastfeeding.
  • Relevant skin conditions at wearable placement sites (e.g., upper arm).
  • BMI \<25 kg/m² confirmed at enrollment.
  • FPG ≥7.0 mmol/L and/or HbA1c ≥6.5% (newly identified type 2 diabetes); Individuals who meet type-2 diabetes criteria at enrollment, based on Swiss/ADA diagnostic criteria will be informed of blood test results and referred to a GP. These individuals will be deemed ineligible and excluded from the study.
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
200 participants (estimated)
Patient registry
No

Groups and cohorts

  • Prediabetic

    Adults aged ≥45 years with BMI ≥25 kg/m². FPG 5.6-6.9 mmol/L and/or HbA1c 5.7-6.4% (clinical prediabetes thresholds). No known type-2 diabetes diagnosis.

  • Normoglycemic

    Adults aged ≥45 years with BMI ≥25 kg/m². FPG \<5.6 mmol/L and HbA1c \<5.7% (normoglycemic; no prediabetes). No known type-2 diabetes diagnosis.

06

What researchers measure

Primary outcomes

  1. Diabetes risk status (prediabetic vs. normoglycemic)

    Prediabetic (FPG levels 5.6-6.9mmol/L and/or HbA1c levels 5.7%-6.4%) Normoglycemic (FPG levels \<5.6mmol/L and HbA1c levels \<5.7%)

    Time frame: At follow-up, week 4

Secondary outcomes

  1. Diabetes risk at alternative FPG and HbA1c thresholds

    Participants will also be classified using alternative FPG and HbA1c thresholds based on the observed distribution of glycemic values in the resulting study sample (e.g., high-risk prediabetes FPG ≥6.0 mmol/L, HbA1c ≥6.0%). Additionally, continuous FPG and HbA1c values will be analyzed.

    Time frame: At follow-up, week 4

  2. Metabolic phenotypes

    Metabolic phenotypes defined based on a combination of FPG, HbA1c, body mass index (BMI) and visceral fat levels.

    Time frame: At follow-up, week 4

  3. Continuous glycemic control

    Continuous glucose levels (mmol/L) over the \~4-week period to characterize dynamic glucose patterns.

    Time frame: Up to 4 weeks

  4. Lifestyle profiles

    Lifestyle patterns derived based on nutrition (e.g., macro-nutrient composition), physical activity, sleep, stress levels (e.g., survey-based, HR/HRV).

    Time frame: Up to 4 weeks

  5. Adherence to image-based food tracking

    Number of meal logs completed

    Time frame: Up to 4 weeks

07

Study locations

1 of 1 sites recruiting
  • HOCH Health and School of Medicine, University of St. Gallen
    Sankt Gallen, 9000, Switzerland
    • Mia Jovanova, Dr. · Contact · +41 44 632 05 41
    • · Contact · mia.jovanova@unisg.ch
    • Mia Jovanova, Dr. · Principal investigator
    • Tobias Kowatsch, Prof. Dr. · Principal investigator
    • Michael Brändle, Prof. Dr. med · Principal investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 28, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07373418
Lead sponsor
University of St.Gallen
Responsible party
Sponsor
First posted
Jan 28, 2026
Start date
Dec 8, 2025
Primary completion
Jan 2027 (estimated)
Completion
Jan 2027 (estimated)
Last update
Jan 28, 2026

Study contacts

Mia Jovanova, Dr.
Contact
mia.jovanova@unisg.ch
+41 44 632 05 41

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion