New study tracks Real-Life workouts and glucose in type 1 diabetes
NCT ID NCT07015970
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study followed 87 active adults with type 1 diabetes who use automated insulin pumps and exercise at least twice a week. Researchers tracked their blood sugar levels before, during, and after exercise to see how well the pumps handle physical activity. The goal was to learn more about glucose control in real-life conditions, not to test a new treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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87 people
The number who actually took part.
- Started
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Mar 2024
- Finished
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Dec 2024
- 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.
Who is studied
The study population will be recruited by four specialized tertiary diabetes care centers (Vandœuvre-lès-Nancy, Strasbourg, Caen, and Mainvilliers).
- Ages
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18 years and older
- 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: * Adult participants with diabetes mellitus type 1 * User for at least 3 months of one the three automated insulin delivery systems available in France at the time of the study (Minimed 780G pump + Guardian 4 sensor + PID-IFB algorithm; or T:Slim X2 pump + Dexcom G6 sensor + Control-IQ algorithm; or mylife Ypsopump + Dexcom G6 sensor + CamAPS FX app) * Engaged in regular physical activity as part of daily life (at least 2 structured sessions per week, each lasting more than 30 minutes) * Able to download data from the pump * Willing and able to complete the physical activity log and self-questionnaires in French * Having received the information sheet and given their oral consent (non-opposition) to participate in the study and for their data processing Exclusion Criteria: * Participants currently enrolled in a clinical trial * Pregnancy or breastfeeding women or women planning a pregnancy during the study * Adults under legal protection (guardianship, curatorship, or judicial safeguard) * Participants with decompensated retinopathy * Participants with decompensated cardiac disease * History of severe hypoglycemia during physical activity in the past 6 months * Participants with unresolved diabetic foot trophic disorders
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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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CHRU of Nancy
Nancy, 54511, France
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CHU of Caen
Caen, 14033, France
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Institute of Diabetology
Mainvilliers, 28300, France
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University Hospitals of Strasbourg
Strasbourg, 67091, France
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