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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02631265
Other study ID # RIDE-1
Secondary ID
Status Completed
Phase N/A
First received December 10, 2015
Last updated September 12, 2017
Start date January 2016
Est. completion date September 2017

Study information

Verified date September 2017
Source Institut de Recherches Cliniques de Montreal
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date September 2017
Est. primary completion date September 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise 1
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).
Exercise 2
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).
Exercise 3
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).

Locations

Country Name City State
Canada Institut de recherches cliniques de Montréal Montreal Quebec

Sponsors (1)

Lead Sponsor Collaborator
Institut de Recherches Cliniques de Montreal

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of time of capillary blood glucose levels spent below 4 mmol/L This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15 This outcome will be measured over 45 minutes.
Secondary Decrease in glucose levels 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 This outcome will be measured over 45 minutes.
Secondary Decremental area under the curve of sensor glucose levels This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15 This outcome will be measured over 45 minutes.
Secondary Area under the curve of sensor glucose levels < 4 mmol/L This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15 This outcome will be measured over 45 minutes.
Secondary Number of patients with an exercise-induced hypoglycemia < 3.9 mmol/L This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15 This outcome will be measured over 45 minutes.
Secondary Number of patients with an exercise-induced hypoglycemia < 3.5 mmol/L This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15 This outcome will be measured over 45 minutes.
Secondary Number of patients requiring an oral treatment for hypoglycemia This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15 This outcome will be measured over 45 minutes.
Secondary Total number of hypoglycemia episode requiring treatment This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15 This outcome will be measured over 45 minutes.
Secondary Percentage of time spent between 4 and 10 mmol/L This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15 This outcome will be measured over 45 minutes.
Secondary Mean time (minutes) to the first hypoglycemic event This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15 This outcome will be measured over 45 minutes.
Secondary Percentage of time spent < 4.0 mmol/L This time frame corresponds to the post-exercise period, from the end of the exercise until 7:00 the next morning. This outcome will be measured over 14.75 hours.
Secondary Percentage of time of sensor glucose levels spent below 4 mmol/L This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15 This outcome will be measure over 45 minutes
Secondary Absolute difference between capillary blood glucose levels and sensor glucose levels This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15 This outcome will be measure over 45 minutes
Secondary Relative difference between capillary blood glucose levels and sensor glucose levels This time frame corresponds to the exercise period. The exercise period will be from 15:30 to 16:15 This outcome will be measure over 45 minutes
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