Physical Activity to Prevent and Treat Hyperglycemia From a Mistimed Bolus Insulin Dose
Recruiting now · Not applicable
Conditions studied: Type 1 Diabetes Mellitus
In brief
People living with type 1 diabetes (PwT1D) are recommended to administer insulin 10-15 minutes before meal consumption (pre-bolus), to account for the delay in the glucose lowering action associated with subcutaneously administered insulin. Due to the demands of day-to-day life, pre-bolusing is not always possible or may be forgotten. With continuous glucose monitors (CGMs), PwT1D may be alerted to this missed insulin dose by a CGM alert, including rapidly rising glucose (change \>2.5mmol/L/15min) or hyperglycemia (\>10.0 mmol/L), and deliver a mistimed (post-prandial) dose in response to CGM alert. This study was designed to determine the effect of combining a post-prandial/mistimed insulin dose with 15 minutes of brisk walking. It is expected that walking will help to minimize or prevent hyperglycemia after a mistimed bolus insulin dose, as well as blunt the rise in glucose following a mistimed insulin dose.
Key facts
- Study ID
- NCT06686329
- Run by
- Jane Yardley
- People needed
- 30
- Starts
- 2025-03-17
- Expected to finish
- 2026-09-30
- Last updated by the study team
- 2026-03-12
Who can join
Age: 18 and older, up to 24. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults aged 18-24 years
- Type 1 diabetes diagnostic for at least two years
- Estimated glycated hemoglobin or glucose management indicator obtained from the past 30 days of CGM data of < 9.9%
- Use a Dexcom G7 CGM in routine care
You may not qualify if…
- Changes in insulin management strategy within the past 2 months
- Diagnosis of gastroparesis
- Having a condition that could render exercise harmful
- Intolerance to gluten and lactose
- Having significant renal disease (e.g., eGRF < 30 ml/min)
- Inability to provide informed consent due to cognitive deficit
- Currently taking other medications (other than insulin) that may alter glucose metabolism (e.g., non-insulin antihyperglycemic drugs such as sglt2-inhibitors, corticosteroids), unless dosages thereof have been stable for more than three months
- For women, being pregnant or breastfeeding
Where it is running
- Institut de recherches cliniques de Montréal — Montreal, Quebec, Canada (enrolling)
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.