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Insulin-based Strategies to Prevent Hypoglycemia During Exercise

Reduction of Basal Insulin to Prevent Hypoglycemia During Exercise in Adults With Type 1 Diabetes Using Insulin Pump Therapy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02631265
Enrollment
22
Registered
2015-12-16
Start date
2016-01-31
Completion date
2017-09-30
Last updated
2017-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 1 Diabetes

Keywords

Type 1 diabetes, Exercise, Hypoglycemia, Insulin pump

Brief summary

It has been reported that insulin basal rate reduction initiated at exercise onset can reduce the hypoglycemic risk during exercise. However, another potentially more efficient strategy to prevent exercise-induced hypoglycemia could be to reduce insulin basal rate a certain time prior to exercise. No study investigated what would be the best timing to initiate such temporary basal insulin reduction. Therefore, the objective of this study will be to compare the efficacy of three strategies to prevent exercise-induced hypoglycemia during a 45 min exercise at 60% VO2peak (moderate intensity): 1) reduce insulin basal rate at the time of exercise; 2) reduce insulin basal rate 20 minutes prior to exercise; 3) reduce insulin basal rate 40 minutes prior to exercise. Investigators hypothesize that the time spent in hypoglycemia will be less when the insulin basal rate is reduced 40 minutes prior to exercise compared to a reduction at the time of exercise. Secondary hypotheses are: 1) Time spent in hypoglycemia will be less when the insulin basal rate is reduced 20 minutes prior to exercise compared to a reduction at the time of exercise; 2) Time spent in hypoglycemia will be less when the insulin basal rate is reduced 40 minutes prior to exercise compared to a reduction 20 minutes prior to exercise.

Interventions

Participants will be admitted at IRCM at 14:00. At 15:30, participant's insulin basal rate will be reduced by 80% and participants will perform a 45-minute exercise on the ergocycle at 60% of VO2 peak (moderate intensity). At 16:15, the participant's usual insulin basal rate will be set in the insulin pump and a standardized snack (30g CHO) will be served. At 16:45, the participant will be discharged and will be asked to eat a standardized dinner at home (60g CHO for females and 80g CHO for males).

Participants will be admitted at IRCM at 14:00. At 15:10, participant's insulin basal rate will be reduced by 80%. At 15:30, participants will perform a 45-minute exercise on the ergocycle at 60% of VO2 peak (moderate intensity). At 16:15, the participant's usual insulin basal rate will be set in the insulin pump and a standardized snack (30g CHO) will be served. At 16:45, the participant will be discharged and will be asked to eat a standardized dinner at home (60g CHO for females and 80g CHO for males).

Participants will be admitted at IRCM at 14:00. At 14:50, participant's insulin basal rate will be reduced by 80%. At 15:30, participants will perform a 45-minute exercise on the ergocycle at 60% of VO2 peak (moderate intensity). At 16:15, the participant's usual insulin basal rate will be set in the insulin pump and a standardized snack (30g CHO) will be served. At 16:45, the participant will be discharged and will be asked to eat a standardized dinner at home (60g CHO for females and 80g CHO for males).

Sponsors

Institut de Recherches Cliniques de Montreal
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Males and females ≥ 18 years of old. 2. Clinical diagnosis of type 1 diabetes for at least one year. 3. The subject will have been on insulin pump therapy for at least 3 months. 4. Last (less than 2 months) HbA1c ≤ 12%.

Exclusion criteria

1. Clinically significant microvascular complications: nephropathy (estimated glomerular filtration rate below 40 ml/min), neuropathy (especially diagnosed gastroparesis) or severe proliferative retinopathy as judged by the investigator. 2. Recent (\< 3 months) acute macrovascular event e.g. acute coronary syndrome or cardiac surgery. 3. Abnormal blood panel and/or anemia. 4. Ongoing pregnancy. 5. Severe hypoglycemic episode within two weeks of screening. 6. Other serious medical illness likely to interfere with study participation or with the ability to complete the exercise periods by the judgment of the investigator (e.g. orthopedic limitation). 7. Failure to comply with team's recommendations (e.g. not willing to change pump parameters, etc.).

Design outcomes

Primary

MeasureTime frameDescription
Percentage of time of capillary blood glucose levels spent below 4 mmol/LThis outcome will be measured over 45 minutes.This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15

Secondary

MeasureTime frameDescription
Decremental area under the curve of sensor glucose levelsThis outcome will be measured over 45 minutes.This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15
Area under the curve of sensor glucose levels < 4 mmol/LThis outcome will be measured over 45 minutes.This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15
Number of patients with an exercise-induced hypoglycemia < 3.9 mmol/LThis outcome will be measured over 45 minutes.This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15
Number of patients with an exercise-induced hypoglycemia < 3.5 mmol/LThis outcome will be measured over 45 minutes.This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15
Number of patients requiring an oral treatment for hypoglycemiaThis outcome will be measured over 45 minutes.This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15
Total number of hypoglycemia episode requiring treatmentThis outcome will be measured over 45 minutes.This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15
Decrease in glucose levelsThis outcome will be measured over 45 minutes.Difference between glucose levels at the beginning of the exercise and the lowest glucose level from the start of the exercise until the end of exercise. This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15
Mean time (minutes) to the first hypoglycemic eventThis outcome will be measured over 45 minutes.This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15
Percentage of time spent < 4.0 mmol/LThis outcome will be measured over 14.75 hours.This time frame corresponds to the post-exercise period, from the end of the exercise until 7:00 the next morning.
Percentage of time of sensor glucose levels spent below 4 mmol/LThis outcome will be measure over 45 minutesThis time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15
Absolute difference between capillary blood glucose levels and sensor glucose levelsThis outcome will be measure over 45 minutesThis time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15
Relative difference between capillary blood glucose levels and sensor glucose levelsThis outcome will be measure over 45 minutesThis time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15
Percentage of time spent between 4 and 10 mmol/LThis outcome will be measured over 45 minutes.This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026