Diabetes remission possible without drugs? new trial investigates lifestyle overhaul
NCT ID NCT07207980
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a personalized diet, exercise, sleep, and counseling program can help adults with type 2 diabetes achieve remission. 120 participants will follow the program for 6 months, then be monitored for another 12. The goal is to see if blood sugar levels can return to normal without medication.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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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About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2028
An estimate. End dates often move.
- 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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18 to 80 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Signed informed consent. 2. Men and women aged 18-80 years, inclusive. 3. Confirmed diagnosis of T2DM according to recognized diagnostic criteria 4. Most recent recorded hemoglobin A1c (HbA1c) \> 6.5%. 5. Body Mass Index (BMI) greater than 27 kg/m². Exclusion Criteria: 1. Failure to meet the diagnostic criteria for T2DM in the screening laboratory tests. 2. Being dependent for basic activities of daily living (Barthel score ≤ 90 points). 3. Lack of willingness to cooperate with the follow-up of the lifestyle intervention plan. 4. Presence of serious or terminal comorbidities significantly worsening short- to medium-term prognosis (active cancer, terminal chronic diseases, myocardial infarction within the last 6 months, acute heart failure or NYHA stage ≥ III, etc.). 5. History of ketoacidosis. 6. Presence of criteria or potential autoimmune insulinopenia (abnormal C-peptide, anti-GAD+ antibodies, pattern of basal and/or glucose-stimulated hypoinsulinemia). 7. Cognitive impairment. 8. Weight loss exceeding 5 kg in the past 6 months. 9. Significant changes in physical activity and/or dietary patterns in the past 6 months. 10. History of eating disorders. 11. History of substance abuse. 12. History of severe psychiatric disorders. 13. Pregnancy or intention to become pregnant within the study period.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Parc Sanitari Pere Virgili
Barcelona, Spain
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