Tailored diet shows promise for better diabetes control
NCT ID NCT07037212
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether intensive, personalized nutrition therapy can help adults with type 2 diabetes better control their blood sugar, reduce inflammation, and improve gut health. Forty adults were split into two groups: one received weekly one-on-one nutrition counseling for 12 weeks, while the other got standard dietary advice. Researchers measured changes in blood sugar levels, inflammatory markers, and gut barrier function to see if the personalized approach leads to better health outcomes.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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40 people
The number who actually took part.
- Started
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Dec 2020
- Finished
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Oct 2022
- Lead sponsor
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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.
- Ages
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20 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosed with Type 2 Diabetes Mellitus (T2DM) for at least one year * Age 20 to 65 years * Body Mass Index (BMI) ≥ 25 kg/m² * Currently receiving oral anti-diabetic (OAD) medications * HbA1c ≥ 7% * Able and willing to provide written informed consent Exclusion Criteria: * Receiving insulin therapy * Presence of uncontrolled comorbid conditions (advanced cardiovascular disease, cerebrovascular disease, severe kidney disease, cancer, or diabetes-related vision impairment) * Presence of acute infection * Taking antioxidant vitamins or mineral supplements * Diagnosed with cognitive impairment or dementia * Using medical devices such as pacemakers or hearing aids * Currently participating in another dietary program * Pregnant or breastfeeding
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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.
Contacts and locations
Locations
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Gazi University Medical Hospital
Ankara, Turkey (Türkiye)
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