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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
University Hospital, Antwerp
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    June 17, 2022
    Last Updated
    August 31, 2022
    Sponsor
    University Hospital, Antwerp
    Collaborators
    Universiteit Antwerpen, York University
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    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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