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Effects of Exercise and Metformin on Methylglyoxal Levels in Prediabetic Individuals

Not Applicable
Completed
Conditions
Methylglyoxal
PreDiabetes
Exercise
Metformin
Registration Number
NCT06603480
Lead Sponsor
Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey
Brief Summary

The aim of this study is to compare the effects of exercise, standard lifestyle changes and metformin on MGO in prediabetic individuals.

Detailed Description

There is no comparative study in the literature evaluating the effects of exercise and metformin on MGO in prediabetic patients. The aim of this study is to compare the effects of exercise, standard lifestyle changes and metformin on MGO in prediabetic individuals.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
96
Inclusion Criteria
  • Patients who were newly diagnosed with prediabetes by Oral Glucose Tolerance Test (OGTT) and/or HbA1C,
  • who were assessed as physically inactive (Level 1) according to the International Physical Activity Questionnaire
  • who had sufficient motivation to participate in the exercise program (assessed by one-on-one interviews conducted by the researchers),
  • who were deemed suitable to participate in the exercise program after a cardiac examination by a cardiologist (with resting electrocardiogram and questioning of cardiac symptoms, and advanced tests such as exercise electrocardiogram test when necessary),
  • who had the same weight (±2.5 kg) for 6 months before participating in the study.
Exclusion Criteria
  • having a serious medical condition that would prevent the person from participating in the exercise study (e.g. advanced malignancy or major neurological, psychiatric or endocrine disease, respiratory failure, etc.),
  • having used metformin for 6 months before the study, having cardiovascular disease,
  • heart failure, cancer, having a BMI <19 kg/m2, receiving hormone replacement therapy,
  • having a life expectancy of less than 1 year, being HIV positive, substance use,
  • functional dependence, having an orthopedic disease that prevents physical activity,
  • having cognitive impairment and other diseases that would affect the study results (respiratory diseases, muscle diseases, non-alcoholic fatty liver disease, etc.),
  • using medications or supplements that would affect the study results.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
MGO1 week

Methylgloxal level

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Sultan 2. Abdülhamid Han Training and Research Hospital

🇹🇷

Üsküdar, İstanbul, Turkey

Sultan 2. Abdülhamid Han Training and Research Hospital
🇹🇷Üsküdar, İstanbul, Turkey

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