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Carbohydrate and Insulin Requirements During Prolonged Fasted Exercise

Primary Purpose

Type 1 Diabetes

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Exercise strategies
Sponsored by
York University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Type 1 Diabetes focused on measuring Physical Activity, Exercise, Carbohydrates, Hypoglycemia, Continuous Glucose Monitoring

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Clinical diagnosis of presumed autoimmune type 1 diabetes
  • Last HbA1c ≤ 9.9 percent
  • Age: 17+ years
  • Duration of T1D: ≥ 1.5 years
  • Using insulin pump therapy: ≥3 months (at least 0.25 units of insulin per kilogram of body mass)
  • In good general health with no conditions that could impact the outcome of the trial
  • Willing to adhere to the protocol requirements for the duration of the study

Exclusion Criteria:

  • Physician diagnosis of active diabetic retinopathy that could be worsened by exercise
  • Physician diagnosis of peripheral neuropathy or autonomic neuropathy
  • Medications:

    1. Beta-blockers
    2. Agents that affect hepatic glucose production (xanthine derivatives)
    3. Pramlintide
    4. Any other hypoglycemic agent
  • Participation in other studies involving the administration of an investigational drug or device during the duration of the current study
  • Severe hypoglycemia in the last 3 months, defined as the individual requiring third party assistance or hospitalization

Sites / Locations

  • York University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Other

Other

Arm Label

Carbohydrate (CHO)-only

50 Percent Basal Rate Reduction (BRR)

Combo

Arm Description

Carbohydrate dose of 0.3g/kg/hr given every 30 minutes of exercise if blood glucose is in range with usual basal insulin infusion

A 50 percent basal rate reduction set 90-minutes pre-exercise and throughout exercise

The combination of a 50 percent basal rate reduction and carbohydrate dose of 0.3g/kg/hr (given every 30 minutes) both at exercise onset

Outcomes

Primary Outcome Measures

Time in glucose target range during exercise intervention
The primary outcome measurement is to determine which strategy had the best time in blood glucose target range (4.0-10.0 mmol/L) during the prolonged exercise

Secondary Outcome Measures

Recovery Interstitial Glucose
Using CGM to measure recovery glucose levels post-exercise to analyze time in target range, time in hypoglycemia (< 4.0 mmol/L) and time in hyperglycemia (> 10.0 mmol/L).

Full Information

First Posted
May 6, 2020
Last Updated
May 6, 2020
Sponsor
York University
Collaborators
Insulet Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT04383015
Brief Title
Carbohydrate and Insulin Requirements During Prolonged Fasted Exercise
Official Title
Carbohydrate Requirements for Prolonged, Fasted Exercise With and Without Basal Rate Reductions in Individuals With Type 1 Diabetes on Continuous Subcutaneous Insulin Infusion
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
October 31, 2018 (Actual)
Primary Completion Date
October 16, 2019 (Actual)
Study Completion Date
October 17, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
York University
Collaborators
Insulet Corporation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare the time spent in glucose target range (4.0-10.0 mmol/L) during exercise and in recovery using three different management strategies for prolonged aerobic exercise: A) carbohydrate dose of 0.3g/kg/hr; B) A 50 percent basal rate reduction, performed 90-minutes in advance of exercise for the duration of the activity; and C) A 50 percent basal rate reduction, performed at exercise onset, with carbohydrate dose of 0.3g/kg/hr
Detailed Description
This project focuses on the effectiveness of various exercise strategies on the time spent in target range during and after aerobic exercise in adults with type 1 diabetes (T1D) on continuous subcutaneous insulin infusion (CSII). The primary objective of the protocol is to determine if a moderate basal insulin reduction (-50 percent of basal), performed 90-minutes before a 120-minute aerobic exercise session (with 5-minute breaks every 30 minutes of exercise, and a ten minute break mid-exercise), improves the time in target range compared to either a carbohydrate consumption only strategy or insulin reduction (-50 percent) and carbohydrate consumption strategy both performed at the onset of exercise in patients with T1D on CSII therapy. The time in target will be determined for both the exercise period and during a 24-hour window after the end of exercise. In all three sessions, aerobic exercise (brisk walking) will be performed in the fasted state (minimum 8 hours after the last meal) in the early-morning. The exercise will consist of four 30-minute bouts of walking at 40-50 percent of the participant's pre-determined aerobic capacity, separated by 5-10 minute breaks. The participants exercise intensity will be monitored continuously using heart rate and activity monitors. Blood glucose and blood ketone levels will be monitored throughout exercise. Each participant will be assigned to a sequence of the three experimental visits through a randomization process. Each exercise session will be separated by at least two days and participants will be expected to complete all sessions within ~ 12 weeks from the time of the baseline/screening visit. Participants will be instructed to apply a new continuous glucose monitor (CGM) sensor between 1-5 days prior, not to perform moderate-to-vigorous exercise 24 hours prior and refrain from caffeine and alcohol 12 hours prior to each study visit. Participants are also instructed not to eat after 2330h the night before arriving to the laboratory and not to give bolus insulin or perform temporary basal rate changes after 0200h on the morning of the exercise visit. Participants are instructed to try to arrive at the laboratory with their blood glucose between 72-270 mg/dL, with no active bolus insulin according to personal CSII device, in the fasted state. If a bolus of insulin was given prior to the exercise session, the session was rescheduled. Females of reproductive capacity performed all three visits in the early follicular phase (days 1-6 of cycle). Participants arrived at the laboratory between 0600h and 1000h. Exercise start time was between 0700h and 1045h, based on participants' choice, and the timing of exercise was kept consistent within participants. Following each exercise session, the participant will rest for 20-minutes and then leave the laboratory. The participants glucose will be monitored for 24-hours after the standardized exercise. They will also be instructed to perform a standardized basal insulin reduction overnight to help reduce the risk of post-exercise nocturnal hypoglycemia (-20 percent from bedtime for 6 hours).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes
Keywords
Physical Activity, Exercise, Carbohydrates, Hypoglycemia, Continuous Glucose Monitoring

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Patients with type 1 diabetes on insulin pump therapy will remain on their usual insulin regimen. However, we are testing percent basal rate reductions during exercise (50 percent reduction) with or without carbohydrate feeding.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Carbohydrate (CHO)-only
Arm Type
Other
Arm Description
Carbohydrate dose of 0.3g/kg/hr given every 30 minutes of exercise if blood glucose is in range with usual basal insulin infusion
Arm Title
50 Percent Basal Rate Reduction (BRR)
Arm Type
Other
Arm Description
A 50 percent basal rate reduction set 90-minutes pre-exercise and throughout exercise
Arm Title
Combo
Arm Type
Other
Arm Description
The combination of a 50 percent basal rate reduction and carbohydrate dose of 0.3g/kg/hr (given every 30 minutes) both at exercise onset
Intervention Type
Other
Intervention Name(s)
Exercise strategies
Intervention Description
Strategies for exercise in type 1 diabetes to maintain glucose control
Primary Outcome Measure Information:
Title
Time in glucose target range during exercise intervention
Description
The primary outcome measurement is to determine which strategy had the best time in blood glucose target range (4.0-10.0 mmol/L) during the prolonged exercise
Time Frame
140 minutes
Secondary Outcome Measure Information:
Title
Recovery Interstitial Glucose
Description
Using CGM to measure recovery glucose levels post-exercise to analyze time in target range, time in hypoglycemia (< 4.0 mmol/L) and time in hyperglycemia (> 10.0 mmol/L).
Time Frame
24 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of presumed autoimmune type 1 diabetes Last HbA1c ≤ 9.9 percent Age: 17+ years Duration of T1D: ≥ 1.5 years Using insulin pump therapy: ≥3 months (at least 0.25 units of insulin per kilogram of body mass) In good general health with no conditions that could impact the outcome of the trial Willing to adhere to the protocol requirements for the duration of the study Exclusion Criteria: Physician diagnosis of active diabetic retinopathy that could be worsened by exercise Physician diagnosis of peripheral neuropathy or autonomic neuropathy Medications: Beta-blockers Agents that affect hepatic glucose production (xanthine derivatives) Pramlintide Any other hypoglycemic agent Participation in other studies involving the administration of an investigational drug or device during the duration of the current study Severe hypoglycemia in the last 3 months, defined as the individual requiring third party assistance or hospitalization
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Riddell, PhD
Organizational Affiliation
York University
Official's Role
Principal Investigator
Facility Information:
Facility Name
York University
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M3J1P3
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

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Carbohydrate and Insulin Requirements During Prolonged Fasted Exercise

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