Mediterranean Diet With Optional Cycling and Rowing to Improve Blood Sugar in Women with Prediabetes
Official title: Continuous Glucose Monitoring During a Mediterranean Diet With Sequential Cycling and Rowing in Women With Prediabetes or Recent Remission From Prediabetes: a Prospective Non-randomised Study Protocol
Run by Marmara University · NCT07326891 · Data updated 2026-11-12
This study tests whether a Mediterranean diet, with or without supervised cycling and rowing, helps women with prediabetes keep their blood sugar in a healthier range.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 22 Years to 55 Years |
| Sex | Women only |
| Enrollment | 30 (estimated) |
| Sponsor | Marmara University Academic / other |
| Locations | 1 site (Beykoz, Istanbul) |
| Status | Recruiting |
| Started | December 15, 2025 |
| Main results expected | October 2026 |
| Study ends | December 2026 |
| Registry record updated | September 15, 2026 |
| Trial ID | NCT07326891 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Women aged 22-55 with prediabetes diagnosed within the last year and meeting fitness criteria for non-strenuous exercise.
✕Probably not a fit
Individuals with diabetes, pregnancy, significant cardiovascular disease, or conditions limiting exercise may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study investigates how a Mediterranean-style diet, alone or paired with supervised cycling and rowing exercises, affects daily blood sugar control in women with prediabetes. Participants are assigned to three groups based on current blood sugar: diet only, diet plus exercise with high blood sugar, and a group with diet plus exercise if currently in normal range. The trial uses continuous glucose monitoring to capture daily glycemic variability in addition to standard tests. The aim is to see if adding structured exercise to the Mediterranean diet improves glycemic control more than diet alone, and whether responders differ by initial glycemic status. The study emphasizes lifestyle modification as a means to reduce progression toward type 2 diabetes.
Why it matters
Potential benefit: If successful, participants could see improved blood sugar control and reduced risk of progressing to diabetes through diet and exercise.
How similar studies have gone: Earlier studies suggest lifestyle changes including diet and exercise can improve glycemic control, though this specific combination with sequential cycling and rowing and CGM is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Having a diagnosis of prediabetes (within the last 1 year) * Impaired Fasting Glucose (IFG) 100-125 mg/dl * OGTT result 2-hour postprandial Impaired Glucose Tolerance (IGT) 140-199 mg/dl * HbA1c 5.7-6.4% * Being between 22-55 years of age * Being female * Body Mass Index 18-34.9 kg/m2 * Meeting the criteria in the American College of Sports Medicine (ACSM) and American Heart Association (AHA) cardiovascular disease risk assessment scoring system * Not engaging in regular planned exercise or physical activity (sedentary) Exclusion Criteria: * Diabetes * Being pregnant * No self-reported low iron concentrations or anaemia * Use of medication, insulin, or weight loss injections known to affect lipid and glucose metabolism * Presence of cardiovascular disease * Current smoking or excessive alcohol consumption * Presence of abnormal electrocardiogram (ECG) * Presence of autonomic neuropathy * Presence of uncontrolled hypertension (systolic blood pressure \>135 mmHg, diastolic blood pressure \>85 mmHg) * Joint-muscle-bone injury limiting exercise
Where it's running
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Marmara University
Beykoz, Istanbul, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Begüm Yücesoy Güneysu, PhD (c)
- Email: begum.yucesoy@gmail.com
- Phone: +90-5377964919
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.