cArdiopulmonary exerCise Test Assessing Multiple biOmarkers and Hormones iN Type 1 diabetEs Under Different Circumstances (ACT-ONE)
Primary Purpose
Diabetes Mellitus, Type 1
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
CPET: CardioPulmonary Exercise Test for CSII users
AEX1: Aerobic Exercise Test 1 for CSII users
AEX2: Aerobic Exercise Test 2 for CSII users
CPET: CardioPulmonary Exercise Test for MDI users
AEX1: Aerobic Exercise Test 1 for MDI users
AEX2: Aerobic Exercise Test 2 for MDI users
Sponsored by
About this trial
This is an interventional other trial for Diabetes Mellitus, Type 1 focused on measuring exercise, biomarker, glucose, lactate, ketones, continuous glucose monitoring, hormones
Eligibility Criteria
Inclusion Criteria:
- Duration of type 1 diabetes mellitus >5y
- Subjects willing to sign an informed consent form (ICF)
- Age 18-60y
- Using a continuous glucose monitoring system (preferably Guardian or Dexcom for CSII / Freestyle Libre for MDI)
- For CSII: only hybrid closed loop pumps (HCL)
- For MDI: only Tresiba (degludec) & Toujeo (glargine)
- HbA1c 6-8.0% (blood result up to 3 months old)
- BMI 20-27.5 kg/m2
- The participant should be in the categories 'moderately' to 'highly physically active' according to the IPAQ score
- The Physical Activity Coefficient has not changed (from category1) in the 2 months prior to the first Exercise Test
Exclusion Criteria:
- Being pregnant or having an active pregnancy wish
- Subject not on MDI or CSII
- Musculoskeletal disorder that affects cycling or is a contra-indication for vigorous physical activity
- Cardiorespiratory disease or ECG abnormality that is a contra-indication for vigorous physical activity
- Having an acute illness (e.g. influenza) that interferes with glucose metabolism
- Having a metabolic disorder (different from diabetes) known to have significant interference with glucose metabolism
- Current treatment with drugs known to have significant interference with glucose metabolism, such as systemic corticoids as judged by the investigator
- Presence of concomitant pathology such as heart failure, liver failure, kidney failure (defined as eGFR <45mL/min, blood result up to 12 months old)
- (Severe) food allergies as judged by the investigator
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
CSII users
MDI users
Arm Description
Patients using Continuous Subcutaneous Insulin Infusion (only hybrid closed loop pumps)
Patients using Multiple Daily Injections (only Tresiba and Toujeo as basal insulin)
Outcomes
Primary Outcome Measures
CGM outcomes during and after morning exercise
CGM outcomes, determined as:
Time in range (TIR) 70-180mg/dL
Time below range (TBR) Level 2, <54 mg/dL
Time below range (TBR) Level 1 and 2, <70 mg/dL
Time above range (TAR) Level 1 and 2, >180 mg/dL
Time above range (TAR) Level 2, >250 mg/dL
Secondary Outcome Measures
Change in glucose concentration in venous blood during and after morning exercise test
Glucose levels in mg/dL during and after CardioPulmonary Exercise Test and 2 morning Aerobic Exercise Tests (90 minutes at 40-45% of VO2 max) (CPET & AEX1-2), measured through EKF
Change in lactate concentration in venous blood during and after morning exercise test
Lactate levels in mM during and after CardioPulmonary Exercise Test and 2 morning Aerobic Exercise Tests (90 minutes at 40-45% of VO2 max) (CPET & AEX1-2), measured through EKF
Change in ketone concentration in venous blood during and after morning exercise test
Ketone (Beta-hydroxybutyrate) levels in mM during and after CardioPulmonary Exercise Test and 2 morning Aerobic Exercise Tests (90 minutes at 40-45% of VO2 max) (CPET & AEX1-2), measured through EKF
Change in cortisol concentration in venous blood during and after morning exercise test
Cortisol levels during and after CardioPulmonary Exercise Test and 2 morning Aerobic Exercise Tests (90 minutes at 40-45% of VO2 max) (CPET & AEX1-2), measured through venous blood sampling analysis
Change in growth hormone concentration in venous blood during and after morning exercise test
Growth hormone levels during and after CardioPulmonary Exercise Test and 2 morning Aerobic Exercise Tests (90 minutes at 40-45% of VO2 max) (CPET & AEX1-2), measured through venous blood sampling analysis
Full Information
NCT ID
NCT05429359
First Posted
June 17, 2022
Last Updated
August 31, 2022
Sponsor
University Hospital, Antwerp
Collaborators
Universiteit Antwerpen, York University
1. Study Identification
Unique Protocol Identification Number
NCT05429359
Brief Title
cArdiopulmonary exerCise Test Assessing Multiple biOmarkers and Hormones iN Type 1 diabetEs Under Different Circumstances
Acronym
ACT-ONE
Official Title
cArdiopulmonary exerCise Test Assessing Multiple biOmarkers and Hormones iN Type 1 diabetEs Under Different Circumstances (ACT-ONE)
Study Type
Interventional
2. Study Status
Record Verification Date
June 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 1, 2022 (Anticipated)
Primary Completion Date
August 31, 2023 (Anticipated)
Study Completion Date
March 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Antwerp
Collaborators
Universiteit Antwerpen, York University
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
Collection of venous blood samples in 50 persons with type 1 diabetes to evaluate the behavior of different biomarkers (glucose, lactate, beta-hydroxybutyrate), and hormones (cortisol, growth hormone) during and after one morning CardioPulmonary Exercise Test and 2 aerobic (90 minutes at 40-45% of VO2 max) exercise tests under different circumstances (see Protocol).
Detailed Description
This study is an extension of the Action-1 pilot study. This study is an extension of the Action-1 pilot study. The aim is to collect samples of multiple biomarkers (circulating glucose, ketones and lactate levels) and hormones (cortisol and growth hormone) during and following an anaerobic and two aerobic exercise in patients with T1D, under more and well-defined circumstances (bolus insulin reduction in combination with major vs. minor basal insulin reduction) to aim for safer glucose levels during and after exercise (~90-180 mg/dL or ~5-10 mmol/L) and avoid extreme glucose excursions to hypo (< 70 mg/dL or <3.9 mmol/L) or hyperglycemia (>180 mg/dL or >10 mmol/L). Based on these data, we aim to formulate exercise guidelines to better help prevent hypoglycemia during and after exercise. Overall, our goal is to help maintain target glycemic values during and after exercise, as evidenced by >70% time in range (70-180mg/dL) while using Continuous Glucose Monitoring (CGM).
Primary endpoint:
• CGM outcomes during and after morning exercise, determined as:
Time in range (TIR) 70-180mg/dL
Time below range (TBR) Level 2, <54 mg/dL
Time below range (TBR) Level 1 and 2, <70 mg/dL
Time above range (TAR) Level 1 and 2, >180 mg/dL
Time above range (TAR) Level 2, >250 mg/dL
Secondary endpoints:
Evaluate values and trends of glucose, lactate and beta-hydroxybutyrate before, during and after morning exercise in venous blood.
Evaluate trends of cortisol and growth hormone before, during and after exercise in relationship to possible hypoglycemic (<70mg/dL glucose) and hyperglycemic events (>180mg/dL).
One CardioPulmonary Exercise Test (CPET, symptom limited maximal exercise test) and two Aerobic Exercise Tests at 40-45% VO2max (AEX), with venous blood samples (catheter), heart rate monitoring during the exercise and follow-up to 6h after the exercise.
(The individual VO2max, using a CardioPulmonary Exercise Test, can be determined during the first "Symptom Limited Maximal" Exercise Test. This to assess the VT1 (V-slope relation VCO2 and VO2; Eq02), VT2 (Relation VE and VCO2; EqCO2) and VO2 peak.)
Before exercise Test 1, the CPET, the study participants will receive 7 questions on the physical activity over the last 7 days (IPAQ questionnaire).
The 3 Exercise Tests will be carried out with 2-4 weeks intervals:
The day before an exercise test and right before, no exercise (only ADL) is allowed (patients should not come to the study center by bike)
The night before the exercise test, no hypoglycemia must occur, as defined by 15 consecutive minutes, or more, of an interstitial glucose <70 mg/dL
Target glucose level in the morning: 90-180 mg/dL
The morning of the exercise test: patients will receive a standardized breakfast (slices of bread with protein spread (containing ±5-25g of protein in total) of in total 0.5g carbohydrates per kg body weight)
Breakfast at 30 minutes before the exercise with a bolus at the start of the breakfast (100% bolus for CPET, 50% bolus for AEX)
Pump settings: basal insulin reduction through temporary target of 150 mg/dL during AEX1 and AEX2 will be adjusted 60-120 minutes prior to the start of the exercise and will last until 60 minutes after the exercise (210-270 min in total)
Lunch (slices of bread with protein spread (containing ±5-25g of protein in total) of in total 0.5g carbohydrates per kg body weight) will be served after 2h of follow-up with a 75% insulin bolus and a correction bolus, if necessary, of 50% of the patient's usual insulin correction dose for the level of hyperglycemia observed.
Hyperglycemia (>250mg/dL) before, during and after exercise will be corrected according to the patient's treatment schedule at 50% of the patient's usual correction factor.
Glucose levels below the target glucose of 90 mg/dL during exercise will be corrected with fast-acting carbohydrates: 15g of oral glucose (sports beverage Aquarius Red Peach (7.4g CHO/100ml)), as repeated every 15 minutes, if necessary, until interstitial and/or whole blood glucose is > 70 mg/dL.
CPET:
Baseline
VO2peak measurement
Breakfast
100% bolus insulin
CSII: 100% basal
MDI: 100% basal
AEX1:
90min
40-45% VO2peak
Breakfast
50% bolus insulin
CSII: -2h target 150 mg/dL
MDI: 50% basal
AEX2:
90min
40-45% VO2peak
Breakfast
50% bolus insulin
CSII: -1h target 150 mg/dL
MDI: 80% basal
CPET = CardioPulmonary Exercise Test; AEX = Aerobic Exercise Test; CSII = Continuous Subcutaneous Insulin Infusion (only hybrid closed loop pumps); MDI = Multiple Daily Injections (only Tresiba and Toujeo as basal insulin)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 1
Keywords
exercise, biomarker, glucose, lactate, ketones, continuous glucose monitoring, hormones
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
CSII users
Arm Type
Active Comparator
Arm Description
Patients using Continuous Subcutaneous Insulin Infusion (only hybrid closed loop pumps)
Arm Title
MDI users
Arm Type
Active Comparator
Arm Description
Patients using Multiple Daily Injections (only Tresiba and Toujeo as basal insulin)
Intervention Type
Other
Intervention Name(s)
CPET: CardioPulmonary Exercise Test for CSII users
Intervention Description
Baseline
VO2peak measurement
Breakfast
100% bolus insulin
CSII users: 100% basal
Intervention Type
Other
Intervention Name(s)
AEX1: Aerobic Exercise Test 1 for CSII users
Intervention Description
90min
40-45% VO2peak
Breakfast
50% bolus insulin
CSII users: -2h target 150 mg/dL
Intervention Type
Other
Intervention Name(s)
AEX2: Aerobic Exercise Test 2 for CSII users
Intervention Description
90min
40-45% VO2peak
Breakfast
50% bolus insulin
CSII users: -1h target 150 mg/dL
Intervention Type
Other
Intervention Name(s)
CPET: CardioPulmonary Exercise Test for MDI users
Intervention Description
Baseline
VO2peak measurement
Breakfast
100% bolus insulin
MDI users: 100% basal
Intervention Type
Other
Intervention Name(s)
AEX1: Aerobic Exercise Test 1 for MDI users
Intervention Description
90min
40-45% VO2peak
Breakfast
50% bolus insulin
MDI users: 50% basal
Intervention Type
Other
Intervention Name(s)
AEX2: Aerobic Exercise Test 2 for MDI users
Intervention Description
90min
40-45% VO2peak
Breakfast
50% bolus insulin
MDI users: 80% basal
Primary Outcome Measure Information:
Title
CGM outcomes during and after morning exercise
Description
CGM outcomes, determined as:
Time in range (TIR) 70-180mg/dL
Time below range (TBR) Level 2, <54 mg/dL
Time below range (TBR) Level 1 and 2, <70 mg/dL
Time above range (TAR) Level 1 and 2, >180 mg/dL
Time above range (TAR) Level 2, >250 mg/dL
Time Frame
CGM values will be collected up to 8 hours prior to the exercise test and 24 hours after the exercise test
Secondary Outcome Measure Information:
Title
Change in glucose concentration in venous blood during and after morning exercise test
Description
Glucose levels in mg/dL during and after CardioPulmonary Exercise Test and 2 morning Aerobic Exercise Tests (90 minutes at 40-45% of VO2 max) (CPET & AEX1-2), measured through EKF
Time Frame
Blood sampling was done before the exercise, every 3-10 minutes during the exercise and every 15 minutes during the first hour of recovery and every 30-60 minutes during the rest of the 6-hour follow-up
Title
Change in lactate concentration in venous blood during and after morning exercise test
Description
Lactate levels in mM during and after CardioPulmonary Exercise Test and 2 morning Aerobic Exercise Tests (90 minutes at 40-45% of VO2 max) (CPET & AEX1-2), measured through EKF
Time Frame
Blood sampling was done before the exercise, every 3-10 minutes during the exercise and every 15 minutes during the first hour of recovery and every 30-60 minutes during the rest of the 6-hour follow-up
Title
Change in ketone concentration in venous blood during and after morning exercise test
Description
Ketone (Beta-hydroxybutyrate) levels in mM during and after CardioPulmonary Exercise Test and 2 morning Aerobic Exercise Tests (90 minutes at 40-45% of VO2 max) (CPET & AEX1-2), measured through EKF
Time Frame
Blood sampling was done before the exercise, every 3-10 minutes during the exercise and every 15 minutes during the first hour of recovery and every 30-60 minutes during the rest of the 6-hour follow-up
Title
Change in cortisol concentration in venous blood during and after morning exercise test
Description
Cortisol levels during and after CardioPulmonary Exercise Test and 2 morning Aerobic Exercise Tests (90 minutes at 40-45% of VO2 max) (CPET & AEX1-2), measured through venous blood sampling analysis
Time Frame
Blood sampling was done before the exercise, every 15-30 minutes during the exercise and every 15-30 minutes during the first hour of recovery and every 60-120 minutes during the rest of the 6-hour follow-up
Title
Change in growth hormone concentration in venous blood during and after morning exercise test
Description
Growth hormone levels during and after CardioPulmonary Exercise Test and 2 morning Aerobic Exercise Tests (90 minutes at 40-45% of VO2 max) (CPET & AEX1-2), measured through venous blood sampling analysis
Time Frame
Blood sampling was done before the exercise, every 15-30 minutes during the exercise and every 15-30 minutes during the first hour of recovery and every 60-120 minutes during the rest of the 6-hour follow-up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Duration of type 1 diabetes mellitus >5y
Subjects willing to sign an informed consent form (ICF)
Age 18-60y
Using a continuous glucose monitoring system (preferably Guardian or Dexcom for CSII / Freestyle Libre for MDI)
For CSII: only hybrid closed loop pumps (HCL)
For MDI: only Tresiba (degludec) & Toujeo (glargine)
HbA1c 6-8.0% (blood result up to 3 months old)
BMI 20-27.5 kg/m2
The participant should be in the categories 'moderately' to 'highly physically active' according to the IPAQ score
The Physical Activity Coefficient has not changed (from category1) in the 2 months prior to the first Exercise Test
Exclusion Criteria:
Being pregnant or having an active pregnancy wish
Subject not on MDI or CSII
Musculoskeletal disorder that affects cycling or is a contra-indication for vigorous physical activity
Cardiorespiratory disease or ECG abnormality that is a contra-indication for vigorous physical activity
Having an acute illness (e.g. influenza) that interferes with glucose metabolism
Having a metabolic disorder (different from diabetes) known to have significant interference with glucose metabolism
Current treatment with drugs known to have significant interference with glucose metabolism, such as systemic corticoids as judged by the investigator
Presence of concomitant pathology such as heart failure, liver failure, kidney failure (defined as eGFR <45mL/min, blood result up to 12 months old)
(Severe) food allergies as judged by the investigator
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Christophe De Block, MD, PhD
Phone
+3238214364
Email
christophe.deblock@uza.be
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christophe De Block, MD, PhD
Organizational Affiliation
University Hospital, Antwerp
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
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cArdiopulmonary exerCise Test Assessing Multiple biOmarkers and Hormones iN Type 1 diabetEs Under Different Circumstances
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