Clinical Trials in France / NCT06803446
Recruiting
Not applicable
Effects of Circadian Rhythm on Glycemic Regulation During Continuous Moderate Exercise and Intense Intermittent Disease in Adolescents Living With Type 1 Diabetes
NCT06803446 · tracked via the Priya Life Science France tracker
Condition(s) studied
Type 1 Diabetes
Investigational drug(s) / intervention(s)
physical test
physical test: continuous and intermittent exercise on cycloergometer
Study summary
Interventional research with minimal risks and constraints on the effects of circadian rhythm on glycemic regulation during intense moderate, continuous and intermittent exercise in adolescents living with type 1 diabetes
Eligibility
Inclusion Criteria:
* Children and adolescents aged 10 to 16;
* Living with type 1 diabetes for at least 1 year with HbA1c less than or equal to 12%;
* Socially insured ;
* Having given their written consent to participate in the research, as well as that of their legal guardians;
* Willing to comply with all research procedures and duration.
Exclusion Criteria:
* Clinically significant microvascular complications: nephropathy (estimated glomerular filtration rate less than 40 ml/min), neuropathy or severe proliferative retinopathy as assessed by the investigator;
* Recent acute macrovascular event (\< 3 months), e.g. acute coronary syndrome or cardiac surgery;
* Abnormal blood picture and/or anemia;
* Current pregnancy;
* Other serious medical condition likely to interfere with study participation or ability to complete exercise periods in the judgment of the investigator (e.g., orthopedic limitation);
* Inability to receive informed information;
* Inability to participate in the entire study;
* Lack of social security coverage;
* Refusal to sign the consent form.
Primary outcome measure(s)
- Comparison of glycemic variation between the 4 conditions — 1 year 10 months september 2026
Observation of time in target, time in hypoglycemia and time in hyperglycemia
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Eurasport | Loos | Nord | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06803446 on ClinicalTrials.gov ↗ ← All trials in France