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Effects of Frequency and Duration of Exercise in People With Type 1 Diabetes A Randomized Crossover Study

Primary Purpose

Diabetes Mellitus, Type 1, Insulin Hypoglycemia

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
"Five sessions per period" - "Two sessions per period"
"Two sessions per period" - "Five sessions per period"
Sponsored by
Steno Diabetes Center Copenhagen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 1 focused on measuring Exercise, Insulin pump, Diabetes Mellitus, Type 1, Guidelines

Eligibility Criteria

18 Years - 64 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Type 1 Diabetes ≥ 2 year
  • Insulin pump ≥ 1 year.
  • Use of carbohydrate counting and the insulin pump bolus calculator for all meals

Exclusion Criteria:

  • Use of anti-diabetic medicine (other than insulin), per oral or injected corticosteroids or other drugs affecting glucose metabolism during the intervention period or within 30 days prior to study start
  • Known or suspected alcohol or drug abuse
  • Other concomitant medical or psychological condition that according to the investigator's assessment makes the participant unsuitable for study participation
  • Females who are pregnant, breast-feeding or intend to become pregnant or are not using adequate contraceptive methods
  • Inability to understand the participants' information and to give informed consent
  • Chronic use or unable to stop acetaminophen (paracetamol) use
  • Allergy to the patch of CGM
  • Hypoglycemia unawareness, quantified by Pedersen-Bjergaard
  • Severe hypoglycemia within the last year
  • Vigorous-intensity exercise for more than 60 minutes on 3 days or more per week

Sites / Locations

  • Steno Diabetes Center Copenhagen

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

1. "Five sessions per period" - "Two sessions per period"

2. "Two sessions per period" - "Five sessions per period"

Arm Description

Outcomes

Primary Outcome Measures

Percentage of time spent in the hypoglycemic range (CGM <3.9 mmol/l)
Intention-to-treat analysis (ITT).

Secondary Outcome Measures

Percentage of time spent in the hypoglycemic range (CGM <3.9 mmol/l)
Per protocol analysis (PP)
Percentage of time spent in the alert and clinical hypoglycemic range
Level 1 (alert): CGM or SMBG value of 3.0-3.9 mmol/l with or without symptoms. Level 2 (clinical): CGM or SMBG value of < 3.0 mmol/l with or without symptoms. Outcome is compared between the two intervention periods in a per protocol analysis (PP) and intention-to-treat analysis (ITT)
Percentage of time spent in the alert and clinical hypoglycemic range
Level 1 (alert): CGM or SMBG value of 3.0-3.9 mmol/l with or without symptoms. Level 2 (clinical): CGM or SMBG value of < 3.0 mmol/l with or without symptoms. Outcome is also compared between the two intervention periods in a per protocol analysis (PP) and intention-to-treat analysis (ITT)
Percentage of time spent in the alert and clinical hypoglycemic range
Level 1 (alert): CGM or SMBG value of 3.0-3.9 mmol/l with or without symptoms. Level 2 (clinical): CGM or SMBG value of < 3.0 mmol/l with or without symptoms. Outcome is also compared between the two intervention periods in a per protocol analysis (PP) and intention-to-treat analysis (ITT)
Percentage of time spent in the alert and clinical hypoglycemic range
Level 1 (alert): CGM or SMBG value of 3.0-3.9 mmol/l with or without symptoms. Level 2 (clinical): CGM or SMBG value of < 3.0 mmol/l with or without symptoms. Outcome is also compared between the two intervention periods in a per protocol analysis (PP) and intention-to-treat analysis (ITT)
Percentage of time spent in the alert and clinical hypoglycemic range
Level 1 (alert): CGM or SMBG value of 3.0-3.9 mmol/l with or without symptoms. Level 2 (clinical): CGM or SMBG value of < 3.0 mmol/l with or without symptoms. Outcome is compared between the two intervention periods in a per protocol analysis (PP) and intention-to-treat analysis (ITT)
Percentage of time spent in the alert and clinical hypoglycemic range
Level 1 (alert): CGM or SMBG value of 3.0-3.9 mmol/l with or without symptoms. Level 2 (clinical): CGM or SMBG value of < 3.0 mmol/l with or without symptoms. Outcome is compared between the two intervention periods in a per protocol analysis (PP) and intention-to-treat analysis (ITT)
Number of alert and clinical hypoglycemia events
Per protocol analysis and intention-to-treat analysis
Number of alert and clinical hypoglycemia events
Per protocol analysis and intention-to-treat analysis
Number of alert and clinical hypoglycemia events
Per protocol analysis and intention-to-treat analysis
Number of alert and clinical hypoglycemia events
Per protocol analysis and intention-to-treat analysis
Number of alert and clinical hypoglycemia events
Per protocol analysis and intention-to-treat analysis
Number of severe hypoglycemia events during
Per protocol analysis and intention-to-treat analysis
Number of severe hypoglycemia events
Per protocol analysis and intention-to-treat analysis
Number of severe hypoglycemia events
Per protocol analysis and intention-to-treat analysis
Number of severe hypoglycemia events
Per protocol analysis and intention-to-treat analysis
Number of severe hypoglycemia events
Per protocol analysis and intention-to-treat analysis
Number of severe hypoglycemia events
Per protocol analysis and intention-to-treat analysis
Percentage of time in range (3.9-10 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in range (3.9-10 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in range (3.9-10 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in range (3.9-10 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in range (3.9-10 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in range (3.9-10 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in good range (3.9-7.8 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in good range (3.9-7.8 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in good range (3.9-7.8 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in good range (3.9-7.8 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in good range (3.9-7.8 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in hyperglycemia (>10 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in hyperglycemia (>10 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in hyperglycemia (>10 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in hyperglycemia (>10 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in hyperglycemia (>10 mmol/l)
Per protocol analysis and intention-to-treat analysis
Percentage of time in hyperglycemia (>10 mmol/l) during all the predefined time blocks. Per protocol analysis and intention-to-treat analysis
Per protocol analysis and intention-to-treat analysis
Glycemic variability measured as standard deviation (SD), coefficient of variation (CV) and low and high blood glucose index (LBGI/HBGI) during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Glycemic variability measured as standard deviation (SD), coefficient of variation (CV) and low and high blood glucose index (LBGI/HBGI) during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Glycemic variability measured as standard deviation (SD), coefficient of variation (CV) and low and high blood glucose index (LBGI/HBGI) during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Glycemic variability measured as standard deviation (SD), coefficient of variation (CV) and low and high blood glucose index (LBGI/HBGI) during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Glycemic variability measured as standard deviation (SD), coefficient of variation (CV) and low and high blood glucose index (LBGI/HBGI) during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Mean CGM glucose level du during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Mean CGM glucose level du during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Mean CGM glucose level du during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Mean CGM glucose level du during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Mean CGM glucose level du during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Mean CGM glucose level du during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
CGM estimated eA1c during the primary intervention period
Per protocol analysis and intention-to-treat analysis
Total carbohydrate intake registered from the insulin pumps during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Total carbohydrate intake registered from the insulin pumps during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Total carbohydrate intake registered from the insulin pumps during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Total carbohydrate intake registered from the insulin pumps during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Total carbohydrate intake registered from the insulin pumps during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Total carbohydrate intake registered from the insulin pumps during all the predefined time blocks in the intervention period
Per protocol analysis and intention-to-treat analysis
Carbohydrate interventions for prevention and treatment of hypoglycemia registered by the participants in the booklet for the primary and total intervention period
Per protocol analysis and intention-to-treat analysis c) Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Carbohydrate interventions for prevention and treatment of hypoglycemia registered by the participants in the booklet for the primary and total intervention period
Per protocol analysis and intention-to-treat analysis c) Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Change in total daily insulin dose (basal and bolus insulin) of 7 days prior to screening day and during the primary and total intervention period
Per protocol analysis and intention-to-treat analysis
Change in total daily insulin dose (basal and bolus insulin) of 7 days prior to screening day and during the primary and total intervention period
Per protocol analysis and intention-to-treat analysis
Actigraph wrist wear time during all predefined time blocks
Per protocol analysis and intention-to-treat analysis
Actigraph wrist wear time during all predefined time blocks
Per protocol analysis and intention-to-treat analysis
Actigraph wrist wear time during all predefined time blocks
Per protocol analysis and intention-to-treat analysis
Actigraph wrist wear time during all predefined time blocks
Per protocol analysis and intention-to-treat analysis
Actigraph wrist wear time during all predefined time blocks
Per protocol analysis and intention-to-treat analysis
Physical activity energy expenditure (accelerometer and heart rate based) measured as kcal during all predefined time blocks
Per protocol analysis and intention-to-treat analysis
Physical activity energy expenditure (accelerometer and heart rate based) measured as kcal during all predefined time blocks
Per protocol analysis and intention-to-treat analysis
Physical activity energy expenditure (accelerometer and heart rate based) measured as kcal during all predefined time blocks
Per protocol analysis and intention-to-treat analysis
Physical activity energy expenditure (accelerometer and heart rate based) measured as kcal during all predefined time blocks
Per protocol analysis and intention-to-treat analysis
Physical activity energy expenditure (accelerometer and heart rate based) measured as kcal during all predefined time blocks
Per protocol analysis and intention-to-treat analysis
Metabolic expenditure rate for the primary intervention periods
Per protocol analysis and intention-to-treat analysis
Metabolic expenditure rate for the primary intervention periods
Per protocol analysis and intention-to-treat analysis
Number of exercise (light to vigorous) and sedentary bouts in the primary intervention period
Per protocol analysis and intention-to-treat analysis
Number of exercise (light to vigorous) and sedentary bouts in the primary intervention period
Per protocol analysis and intention-to-treat analysis
Time in sedentary during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in sedentary during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in sedentary during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in sedentary during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in sedentary during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in light physical activity during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in light physical activity during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in light physical activity during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in light physical activity during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in moderate physical activity during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in moderate physical activity during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in moderate physical activity during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in moderate physical activity during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in vigorous physical activity during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in vigorous physical activity during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in vigorous physical activity during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Time in vigorous physical activity during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Number of steps during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Number of steps during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Number of steps during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Number of steps during predefined time blocks
Per protocol analysis and intention-to-treat analysis
Heart rate during exercise sessions
Per protocol analysis and intention-to-treat analysis
R-R intervals during exercise sessions (f)
Per protocol analysis and intention-to-treat analysis
Sleep latency (min) during the primary and total intervention period
Per protocol analysis and intention-to-treat analysis
Sleep latency (min) during the primary and total intervention period
Per protocol analysis and intention-to-treat analysis
Total sleep time (min) during the primary and total intervention period
Per protocol analysis and intention-to-treat analysis
Total sleep time (min) during the primary and total intervention period
Per protocol analysis and intention-to-treat analysis
Sleep efficiency (%) during the primary and total intervention period
Per protocol analysis and intention-to-treat analysis
Sleep efficiency (%) during the primary and total intervention period
Per protocol analysis and intention-to-treat analysis
Number of awakening during sleep in the primary and total intervention period
Per protocol analysis and intention-to-treat analysis
Number of awakening during sleep in the primary and total intervention period
Per protocol analysis and intention-to-treat analysis
Time of awakening during sleep in the primary and total intervention period
Per protocol analysis and intention-to-treat analysis
Time of awakening during sleep in the primary and total intervention period
Per protocol analysis and intention-to-treat analysis
Question about patient preference regarding the two study arms
Per protocol analysis and intention-to-treat analysis

Full Information

First Posted
September 5, 2019
Last Updated
September 27, 2021
Sponsor
Steno Diabetes Center Copenhagen
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1. Study Identification

Unique Protocol Identification Number
NCT04089462
Brief Title
Effects of Frequency and Duration of Exercise in People With Type 1 Diabetes A Randomized Crossover Study
Official Title
Effects of Frequency and Duration of Exercise in People With Type 1 Diabetes - A Randomized Crossover Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
September 30, 2019 (Actual)
Primary Completion Date
October 15, 2020 (Actual)
Study Completion Date
January 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Steno Diabetes Center Copenhagen

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
According to the Standards of Medical Care in Diabetes by the American Diabetes Association, people with diabetes should aim for 30 minutes of moderate-to-vigorous intensity aerobic exercise at least 5 days a week or a total of 150 minutes per week and doing some type of strength training at least 2 times per week in addition to aerobic activity. However, the effects of different forms and intervals of exercise on glycemic control are not well established. Exercise increases the risk of hypoglycemia both during and several hours after exercise. There are several strategies to avoid hypoglycemia during exercise. The most common strategy is to reduce insulin and to take carbohydrates before the exercise starts. Short-acting insulin analogs have a duration of approximately four hours, thus reductions need to be planned and done well in advance before the exercise starts. Since different types of exercise (aerobic, strength training or high intensity training) affect blood glucose in different ways and most exercise sessions include a combination of the types, these strategies are often associated with difficulties in obtaining stable blood glucose. The American Diabetes Association guidelines do not explicitly recommend a daily workout routine but outline recommendations for weekly amounts of exercise as there is currently insufficient evidence on the ideal timing, frequency and duration of exercise for preventing hypoglycemia. Hypothesis: in people with type 1 diabetes, time in hypoglycemia can be reduced if exercise is performed daily over five consecutive days compared to the same total amount of exercise performed at 2 days with at least 2 days interval. Aim: to evaluate the impact of the same total amount of exercise split into either five consecutive sessions or two sessions with at least 2 days in between on percentage of time spent in hypoglycemia and other glycemic parameters in people with type 1 diabetes.
Detailed Description
The participants will go through two interventions: Exercise one session per day for five consecutive days and Exercise one session per day for two days within five days. The exercise session will start with anaerobic (push-ups, back-curls, sit-ups, triceps-dips and jumps) exercise followed by aerobic exercise (moderate intensity of running, walking or cycling). Between the two intervention periods, there will be a wash-out period. Intervention: 'Exercise one session per day for five consecutive days'. Duration per session: Anaerobic: 4 min, Aerobic: 30 min. Sessions per intervention period: Five. Total duration per intervention period: Anaerobic: 20 min. Aerobic: 150 min. Total: 170 min Intervention:Exercise one session per day for two days within five days. Duration per session: Anaerobe: 10 min, Aerobe: 75 min. Sessions per intervention period: 2. Total duration per intervention period: Anaerob: 20 min Aerobe: 150 min Total: 170 min

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 1, Insulin Hypoglycemia
Keywords
Exercise, Insulin pump, Diabetes Mellitus, Type 1, Guidelines

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
An open-labelled randomized controlled crossover study will be performed. The participants will go through the following elements: Screening day Run-in period Intervention period Wash-out period Intervention period
Masking
None (Open Label)
Allocation
Randomized
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1. "Five sessions per period" - "Two sessions per period"
Arm Type
Other
Arm Title
2. "Two sessions per period" - "Five sessions per period"
Arm Type
Other
Intervention Type
Behavioral
Intervention Name(s)
"Five sessions per period" - "Two sessions per period"
Intervention Description
Period 1: 5 exercise sessions on 5 consecutive days (4 min anaerobic exercise and 30 min aerobic exercise per session) Period 2: 2 exercise sessions within a 5-day period (10 min anaerobic exercise and 75 min aerobic exercise per session)
Intervention Type
Behavioral
Intervention Name(s)
"Two sessions per period" - "Five sessions per period"
Intervention Description
Period 1: 2 exercise sessions within a 5-day period (10 min anaerobic exercise and 75 min aerobic exercise per session) Period 2: 5 exercise sessions on 5 consecutive days (4 min anaerobic exercise and 30 min aerobic exercise per session)
Primary Outcome Measure Information:
Title
Percentage of time spent in the hypoglycemic range (CGM <3.9 mmol/l)
Description
Intention-to-treat analysis (ITT).
Time Frame
The primary intervention period from 06:00h study day 1 - 06:00h study day 6 (ITT)
Secondary Outcome Measure Information:
Title
Percentage of time spent in the hypoglycemic range (CGM <3.9 mmol/l)
Description
Per protocol analysis (PP)
Time Frame
Primary intervention period from 06:00h study day 1 - 06:00h study day 6 PP
Title
Percentage of time spent in the alert and clinical hypoglycemic range
Description
Level 1 (alert): CGM or SMBG value of 3.0-3.9 mmol/l with or without symptoms. Level 2 (clinical): CGM or SMBG value of < 3.0 mmol/l with or without symptoms. Outcome is compared between the two intervention periods in a per protocol analysis (PP) and intention-to-treat analysis (ITT)
Time Frame
Study day 1: The day when the first exercise session is performed and registered.
Title
Percentage of time spent in the alert and clinical hypoglycemic range
Description
Level 1 (alert): CGM or SMBG value of 3.0-3.9 mmol/l with or without symptoms. Level 2 (clinical): CGM or SMBG value of < 3.0 mmol/l with or without symptoms. Outcome is also compared between the two intervention periods in a per protocol analysis (PP) and intention-to-treat analysis (ITT)
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Percentage of time spent in the alert and clinical hypoglycemic range
Description
Level 1 (alert): CGM or SMBG value of 3.0-3.9 mmol/l with or without symptoms. Level 2 (clinical): CGM or SMBG value of < 3.0 mmol/l with or without symptoms. Outcome is also compared between the two intervention periods in a per protocol analysis (PP) and intention-to-treat analysis (ITT)
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Percentage of time spent in the alert and clinical hypoglycemic range
Description
Level 1 (alert): CGM or SMBG value of 3.0-3.9 mmol/l with or without symptoms. Level 2 (clinical): CGM or SMBG value of < 3.0 mmol/l with or without symptoms. Outcome is also compared between the two intervention periods in a per protocol analysis (PP) and intention-to-treat analysis (ITT)
Time Frame
Day time: 06:00-22:00h from during study day 1 to study day 6.
Title
Percentage of time spent in the alert and clinical hypoglycemic range
Description
Level 1 (alert): CGM or SMBG value of 3.0-3.9 mmol/l with or without symptoms. Level 2 (clinical): CGM or SMBG value of < 3.0 mmol/l with or without symptoms. Outcome is compared between the two intervention periods in a per protocol analysis (PP) and intention-to-treat analysis (ITT)
Time Frame
Night time: 22:00-06:00h from during study day 1 to study day 6.
Title
Percentage of time spent in the alert and clinical hypoglycemic range
Description
Level 1 (alert): CGM or SMBG value of 3.0-3.9 mmol/l with or without symptoms. Level 2 (clinical): CGM or SMBG value of < 3.0 mmol/l with or without symptoms. Outcome is compared between the two intervention periods in a per protocol analysis (PP) and intention-to-treat analysis (ITT)
Time Frame
The time the participant has recorded start and end of exercise session during study day 1 to study day 6
Title
Number of alert and clinical hypoglycemia events
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Number of alert and clinical hypoglycemia events
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Number of alert and clinical hypoglycemia events
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h during study day 1 - study day 6
Title
Number of alert and clinical hypoglycemia events
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Night time: 22:00-06:00h during study day 1 - study day 6
Title
Number of alert and clinical hypoglycemia events
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 study day 6
Title
Number of severe hypoglycemia events during
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Study day 1: The day when the first exercise session is performed and registered
Title
Number of severe hypoglycemia events
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Number of severe hypoglycemia events
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Number of severe hypoglycemia events
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h during study day 1 - study day 6
Title
Number of severe hypoglycemia events
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Night time: 22:00-06:00h during study day 1 - study day 6
Title
Number of severe hypoglycemia events
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 - study day 6
Title
Percentage of time in range (3.9-10 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Study day 1: The day when the first exercise session is performed and registered
Title
Percentage of time in range (3.9-10 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Percentage of time in range (3.9-10 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Percentage of time in range (3.9-10 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h during study day 1-study day 6
Title
Percentage of time in range (3.9-10 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Night time: 22:00-06:00h during study day 1 -study day 6
Title
Percentage of time in range (3.9-10 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 -study day 6
Title
Percentage of time in good range (3.9-7.8 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Study day 1: The day when the first exercise session is performed and registered.
Title
Percentage of time in good range (3.9-7.8 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Percentage of time in good range (3.9-7.8 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Percentage of time in good range (3.9-7.8 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h and Night time: 22:00-06:00h during study day 1-study day 6
Title
Percentage of time in good range (3.9-7.8 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1-study day 6
Title
Percentage of time in hyperglycemia (>10 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Study day 1: The day when the first exercise session is performed and registered.
Title
Percentage of time in hyperglycemia (>10 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Percentage of time in hyperglycemia (>10 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h during study day 1-study day 6
Title
Percentage of time in hyperglycemia (>10 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Night time: 22:00-06:00h during study day 1 -study day 6
Title
Percentage of time in hyperglycemia (>10 mmol/l)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1-study day 6
Title
Percentage of time in hyperglycemia (>10 mmol/l) during all the predefined time blocks. Per protocol analysis and intention-to-treat analysis
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Glycemic variability measured as standard deviation (SD), coefficient of variation (CV) and low and high blood glucose index (LBGI/HBGI) during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Study day 1: The day when the first exercise session is performed and registered.
Title
Glycemic variability measured as standard deviation (SD), coefficient of variation (CV) and low and high blood glucose index (LBGI/HBGI) during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Glycemic variability measured as standard deviation (SD), coefficient of variation (CV) and low and high blood glucose index (LBGI/HBGI) during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h during study day 1-study day 6
Title
Glycemic variability measured as standard deviation (SD), coefficient of variation (CV) and low and high blood glucose index (LBGI/HBGI) during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Night time: 22:00-06:00h during study day 1 -study day 6
Title
Glycemic variability measured as standard deviation (SD), coefficient of variation (CV) and low and high blood glucose index (LBGI/HBGI) during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 -study day 6
Title
Mean CGM glucose level du during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Study day 1: The day when the first exercise session is performed and registered.
Title
Mean CGM glucose level du during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Mean CGM glucose level du during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Mean CGM glucose level du during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h during study day 1-study day 6
Title
Mean CGM glucose level du during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Night time: 22:00-06:00h during study day 1 -study day 6
Title
Mean CGM glucose level du during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 -study day 6
Title
CGM estimated eA1c during the primary intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
The Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Total carbohydrate intake registered from the insulin pumps during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Study day 1: The day when the first exercise session is performed and registered.
Title
Total carbohydrate intake registered from the insulin pumps during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Total carbohydrate intake registered from the insulin pumps during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Total carbohydrate intake registered from the insulin pumps during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h during study day 1-study day 6
Title
Total carbohydrate intake registered from the insulin pumps during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Night time: 22:00-06:00h during study day 1 -study day 6
Title
Total carbohydrate intake registered from the insulin pumps during all the predefined time blocks in the intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 -study day 6
Title
Carbohydrate interventions for prevention and treatment of hypoglycemia registered by the participants in the booklet for the primary and total intervention period
Description
Per protocol analysis and intention-to-treat analysis c) Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Carbohydrate interventions for prevention and treatment of hypoglycemia registered by the participants in the booklet for the primary and total intervention period
Description
Per protocol analysis and intention-to-treat analysis c) Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days)
Title
Change in total daily insulin dose (basal and bolus insulin) of 7 days prior to screening day and during the primary and total intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Change in total daily insulin dose (basal and bolus insulin) of 7 days prior to screening day and during the primary and total intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Actigraph wrist wear time during all predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Actigraph wrist wear time during all predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Actigraph wrist wear time during all predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h during study day 1-study day 6
Title
Actigraph wrist wear time during all predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Night time: 22:00-06:00h during study day 1 -study day 6
Title
Actigraph wrist wear time during all predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 -study day 6
Title
Physical activity energy expenditure (accelerometer and heart rate based) measured as kcal during all predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Physical activity energy expenditure (accelerometer and heart rate based) measured as kcal during all predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Physical activity energy expenditure (accelerometer and heart rate based) measured as kcal during all predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h during study day 1-study day 6
Title
Physical activity energy expenditure (accelerometer and heart rate based) measured as kcal during all predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Night time: 22:00-06:00h during study day 1 -study day 6
Title
Physical activity energy expenditure (accelerometer and heart rate based) measured as kcal during all predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 -study day 6
Title
Metabolic expenditure rate for the primary intervention periods
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Metabolic expenditure rate for the primary intervention periods
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Number of exercise (light to vigorous) and sedentary bouts in the primary intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Number of exercise (light to vigorous) and sedentary bouts in the primary intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days)
Title
Time in sedentary during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Time in sedentary during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Time in sedentary during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h during study day 1-study day 6
Title
Time in sedentary during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Night time: 22:00-06:00h during study day 1 -study day 6
Title
Time in sedentary during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 -study day 6
Title
Time in light physical activity during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Time in light physical activity during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Time in light physical activity during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h during study day 1-study day 6
Title
Time in light physical activity during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 -study day 6
Title
Time in moderate physical activity during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Time in moderate physical activity during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days).
Title
Time in moderate physical activity during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h during study day 1-study day 6
Title
Time in moderate physical activity during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 -study day 6
Title
Time in vigorous physical activity during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Time in vigorous physical activity during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days)
Title
Time in vigorous physical activity during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h during study day 1-study day 6
Title
Time in vigorous physical activity during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 -study day 6
Title
Number of steps during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Number of steps during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days)
Title
Number of steps during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Day time: 06:00-22:00h during study day 1-study day 6
Title
Number of steps during predefined time blocks
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 -study day 6
Title
Heart rate during exercise sessions
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 -study day 6
Title
R-R intervals during exercise sessions (f)
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Exercise time: The time the participant has recorded start and end of exercise session during study day 1 -study day 6
Title
Sleep latency (min) during the primary and total intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Sleep latency (min) during the primary and total intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days)
Title
Total sleep time (min) during the primary and total intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Total sleep time (min) during the primary and total intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days)
Title
Sleep efficiency (%) during the primary and total intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Sleep efficiency (%) during the primary and total intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days)
Title
Number of awakening during sleep in the primary and total intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Number of awakening during sleep in the primary and total intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days)
Title
Time of awakening during sleep in the primary and total intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Primary intervention period: 06:00h study day 1 - 06:00h study day 6 (= 5 x 24-hour days)
Title
Time of awakening during sleep in the primary and total intervention period
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
Secondary intervention period: 08:00h day 1 - 08:00h day 8 (= 7 x 24-hour days)
Title
Question about patient preference regarding the two study arms
Description
Per protocol analysis and intention-to-treat analysis
Time Frame
At the end of study. Study day 6 the last interventions period.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Type 1 Diabetes ≥ 2 year Insulin pump ≥ 1 year. Use of carbohydrate counting and the insulin pump bolus calculator for all meals Exclusion Criteria: Use of anti-diabetic medicine (other than insulin), per oral or injected corticosteroids or other drugs affecting glucose metabolism during the intervention period or within 30 days prior to study start Known or suspected alcohol or drug abuse Other concomitant medical or psychological condition that according to the investigator's assessment makes the participant unsuitable for study participation Females who are pregnant, breast-feeding or intend to become pregnant or are not using adequate contraceptive methods Inability to understand the participants' information and to give informed consent Chronic use or unable to stop acetaminophen (paracetamol) use Allergy to the patch of CGM Hypoglycemia unawareness, quantified by Pedersen-Bjergaard Severe hypoglycemia within the last year Vigorous-intensity exercise for more than 60 minutes on 3 days or more per week
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Isabelle IK Steineck, MD
Organizational Affiliation
Steno Diabetes Center Copenhagen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Steno Diabetes Center Copenhagen
City
Gentofte
ZIP/Postal Code
2820
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data are processed and merged into at least one scientific article published in international peer-reviewed scientific journal. Positive, negative and inconclusive results will be published as soon as scientifically justifiable.
IPD Sharing Time Frame
21 oktober 2020
Citations:
PubMed Identifier
33509935
Citation
Steineck IIK, Ranjan AG, Schmidt S, Norgaard K. Time spent in hypoglycemia is comparable when the same amount of exercise is performed 5 or 2 days weekly: a randomized crossover study in people with type 1 diabetes. BMJ Open Diabetes Res Care. 2021 Jan;9(1):e001919. doi: 10.1136/bmjdrc-2020-001919.
Results Reference
derived

Learn more about this trial

Effects of Frequency and Duration of Exercise in People With Type 1 Diabetes A Randomized Crossover Study

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