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Pre DiabeticPRE-GLIDENCT07599072

PREdiabetes GLycemic Impact and Data Evaluation

A study testing CGM Sibionics and On-Call Extra Glucometer in people with Pre Diabetic and Obesity & Overweight, run by Nazarii Kobyliak at 3 sites in Ukraine.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This prospective, randomized controlled trial evaluates whether real-time continuous glucose monitoring (CGM) improves glycemic control and lifestyle adherence in adults with prediabetes compared to conventional self-monitoring methods over a 3-month period. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
CGM Sibionics and On-Call Extra Glucometer
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
80 participants
Where
3 sitesUkraine
Study dates
1 Jul 2026to 30 Jun 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age of 18 years and older.
  • Presence of prediabetes diagnosed according to criteria of the American Diabetes Association
  • Persons who treated with diet and exercise alone or metformin on a stabilized dose for at least 3 months before the study;
  • Ability to comply with protocol requirements and maintain a patient diary.
  • Signed informed consent.

Who cannot join

  • Presence of type 1 or type 2 diabetes;
  • Decompensated liver or kidney diseases (GFR < 45 ml/min/1. 73 m²);
  • Active cardiovascular diseases within 12 months of Visit 1, such as myocardial infarction, clinically significant arrhythmia, unstable angina, coronary artery bypass surgery, or angioplasty; or are expected to require coronary artery bypass surgery or angioplasty during the course of the study;
  • Endocrine disorders (e.g., Itsenko-Cushing syndrome, acromegaly) that affect glycemia;
  • Pregnancy or lactation;
  • Mental or cognitive impairments that would interfere with study participation;
Show all 11Show fewer
  • Daily use of any form of steroid medication (oral, inhaled, injected) within the last 3 months;
  • Recent use of any CGM within the last 12 months;
  • Known allergy to sensor materials;
  • Has evidence of current abuse of drugs or alcohol or a history of abuse that, in the investigator's opinion, would cause the individual to be noncompliant;
  • Participation in another clinical study within the last 3 months.

Trial locations and contacts

3 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Nazarii Kobyliak, Professor contact

+380442356005

nazariikobyliak@gmail.com

Ilona Rudneva, Dr contact

0442356005

ilonarudneva57@gmail.com

Ukraine3 sites, 3 recruiting
  • Bogomoletz Institute of Physiology

    Kyiv, 01024

    Enrolling by invitation
  • Bogomolets National Medical University

    Kyiv, 01601

    Nazarii Kobyliak, Professor, 0442356005, nazariikobyliak@gmail.com

    Victoriia Yerokhovych, PhD, ilonarudneva57@gmail.com

    Recruiting
  • University Hospital of Bogomolets National Medical University

    Kyiv, 01601

    Ilona Rudneva, PhD student, 0442356005, ilonarudneva57@gmail.com

    Ieva Ilkiv, PhD Student, 0442356005, evailkiv333@gmail.com

    Recruiting

Other trials in Ukraine

About this study

Official title: Evaluation of the Impact of Continuous Glucose Monitoring (CGM) Systems on Glycemic Control in People With Prediabetes: Postmarketing Clinical Study

This prospective, randomized controlled trial evaluates whether real-time continuous glucose monitoring (CGM) improves glycemic control and lifestyle adherence in adults with prediabetes compared to conventional self-monitoring methods over a 3-month period. By analyzing metabolic markers and behavioral data, the study aims to determine the effectiveness of 24-hour monitoring as a personalized tool that increases patient adherence to lifestyle changes compared to conventional SMBG methods.

Read the detailed description

Prediabetes is considered a critical stage at which effective prevention of the development of diabetes is possible, provided that early detection and adequate glycemic control. International clinical guidelines and multicenter studies suggest that early intensive glycemic control is associated with a better prognosis and a reduced risk of complications. However, standard self-monitoring has limited information on glycemic variability, which is especially important in the early stages of carbohydrate metabolism disorders, including prediabetes. Routine indicators such as fasting blood glucose, 1 and 2 hours after a meal, and glycated hemoglobin (HbA1c) do not always clearly differentiate between diabetes, prediabetes, and normal carbohydrate metabolism. Recently, there has been a need for more comprehensive blood glucose monitoring strategies that cover the entire spectrum of glycemic variability. Continuous glucose monitoring (CGMs) technology provides real-time glucose concentration data, overcoming the limitations of traditional monitoring methods. Recently, not only among people with diabetes, but also among people with prediabetes, there has been an increasing trend towards using CGM as a personal device to monitor glucose levels and promote healthy habits such as increased activity, diet, and sleep. Their motivation is to improve their own glycemic control and avoid the future development of diabetes and its associated complications, to optimize blood glucose levels to achieve peak mental or physical performance, and to use personal monitoring data to develop sustainable behavioral skills. The contactless 24-hour monitoring system is considered a promising tool for personalized glycemic control, but its use in people with prediabetes has not been studied enough This is a prospective, open-label, randomized controlled trial involving 80 adult patients with prediabetes recruited at the Bogomolets National Medical University. Participants were randomized in a 1:1 ratio to either the Real-Time Continuous Glucose Monitoring (CGM group) or the control group (standard Self-Monitoring of Blood Glucose [SMBG] using conventional glucometers). Participants will undergo a 3-month observation period. The use of the assigned monitoring devices (CGM or SMBG glucometer) and pedometers will last for the first 1 month. The study consists of three visits: Visit 1 (baseline), Visit 2 (1 month, end of intervention), and Visit 3 (3 months, follow-up period). During these visits, researchers will collect data on glycated hemoglobin (HbA1c), fructosamine, Cpeptide, HOMA-IR index, lipid profile, anthropometric indicators (body mass index (BMI), waist circumference), bioimpedance measurement, physical activity monitoring using pedometers, and SF-36 questionnaire to assess quality of life.

The gathered data will help determine whether continuous monitoring provided by CGM systems improves glycemic control and increases patient adherence to lifestyle changes compared to conventional SMBG methods.

Being tested
CGM Sibionics, On-Call Extra Glucometer
Keywords
prediabetes, obesity, continuous glucose monitoring, insulin resistance, traditional glycemia self-monitoring
Medical subject headings
Glucose Intolerance, Obesity, Overweight, Insulin Resistance, Prediabetic State

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • CGM SibionicsDevice

    A registered medical device for real-time monitoring of glucose levels in interstitial fluid.

  • On-Call Extra GlucometerDevice

    Capillary glucose monitoring using fingerstick glucometer as per standard care.

Study groups in NCT07599072
Study groupRoleWhat they receive
CGM groupExperimentalParticipants with prediabetes will be provided with a Real-Time Continuous Glucose Monitoring (RT-CGM) device to monitor their blood glucose along with educational materials to better understand and manage their prediabetes and other supporting services. Pre and post intervention surveys and investigation will be implemented. Participants will be utilizing RT-CGM device for 28 days and then followed up for 3-month participation.
Receives: Device: CGM Sibionics
traditional fingerstick glucometerActive comparatorParticipants with prediabetes will be provided with traditional fingerstick glucometer device to self-monitor their blood glucose along with educational materials to better understand and manage their prediabetes and other supporting services. Pre and post intervention surveys and investigation will be implemented. Participants will be utilizing glucometer with at least 2-3 measurements per week for 28 days and then followed up for 3-month participation.
Receives: Device: On-Call Extra Glucometer

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Changes in HbA1c level

    HbA1c in %

    Measured: at 3 month (end of follow-up period)

  2. Changes in Fructosamine level

    Fructosamine in μmol/L

    Measured: at 3 month (end of intervention period)

Secondary outcomes (11)
  1. Homeostatic Model Assessment of Insulin Resistance (HOMA2-IR)

    HOMA2-IR will be calculated based on fasting plasma glucose and fasting serum insulin levels using the non-linear Homeostasis Model Assessment. The score is continuous, theoretically starting from 0, where higher values indicate greater insulin resistance (a worse clinical outcome).

    Measured: at 3 month (follow-up period) compared to baseline

  2. insulin sensitivity (%S)

    This model can be calculated using the software supplied by the Oxford Centre for Diabetes Endocrinology and Metabolism

    Measured: at 3 month (follow-up period) compared to baseline

  3. β-cell function (%B)

    This model can be calculated using the software supplied by the Oxford Centre for Diabetes Endocrinology and Metabolism

    Measured: at 3 month (follow-up period) compared to baseline

  4. body mass index (BMI)

    weight in kg and height in meters will be combined to report BMI in kg/m^2

    Measured: at 1 month (end of intervention) and 3 month (follow-up period) compared to baseline

  5. waist circumferences (WC)

    WC in cm

    Measured: at 1 month (end of intervention) and 3 month (follow-up period) compared to baseline

  6. visceral fat content

    visceral fat content using electronic scales-analyzers of body composition Huawei (Smart Scale series 3/3 Pro

    Measured: at 1 month (end of intervention) and 3 month (follow-up period) compared to baseline

  7. Total Cholesterol (TC)

    TC in mmol/l

    Measured: at 3 month (follow-up period) compared to baseline

  8. Tryglicerides (TG)

    TG in mmol/l

    Measured: at 3 month (follow-up period) compared to baseline

  9. LDL-Cholesterol (LDL-C)

    LDL-C in mmol/l

    Measured: at 3 month (follow-up period) compared to baseline]

  10. Physical activity levels

    Daily number of steps as measured by a sealed pedometer

    Measured: at 1 month (end of intervention) and 3 month (follow-up period) compared to baseline

  11. Quality of Life Evaluation: Medical Outcomes Study Short-Form 36 (SF-36)

    Health-related quality of life will be evaluated using the Medical Outcomes Study Short-Form 36 (SF-36) questionnaire. The SF-36 consists of 36 items measuring 8 health domains, which are aggregated into two summary scores: the Physical Component Summary (PCS) and the Mental Component Summary (MCS). For each domain and summary score, values are transformed to a scale ranging from a minimum of 0 to a maximum of 100. Higher scores represent better health status and a better quality of life outcome.

    Measured: at 1 month (end of intervention) and 3 month (follow-up period) compared to baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 May 2026
  2. Study start1 Jul 2026
  3. Primary completion31 May 2027 (estimated)
  4. Study completion30 Jun 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
80 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07599072
Sponsor's protocol ID
PRE-GLIDE
Acronym
PRE-GLIDE
Status last verified
Jun 2026
First submitted
14 May 2026
Last updated
29 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing CGM Sibionics and On-Call Extra Glucometer in people with Pre Diabetic and Obesity & Overweight, run by Nazarii Kobyliak at 3 sites in Ukraine.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 29 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in Ukraine. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Nazarii Kobyliak, Professor (+380442356005, nazariikobyliak@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Changes in HbA1c level (time frame: at 3 month (end of follow-up period)). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Sep 2026.

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