Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05179135
Other study ID # BC-09533
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 19, 2022
Est. completion date November 21, 2022

Study information

Verified date December 2021
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A cornerstone in the management and treatment of people living with type 1 diabetes (T1D) is to engage in regular physical exercise for a variety of health and fitness reasons. Despite these well-established benefits, many people with T1D experience their challenging glycaemic condition as a high barrier to exercise. The challenge of managing glycaemia around exercise together with fear of hypoglycaemia (FOH) remain major barriers to exercise in T1D patients, meaning that many are discouraged from exercise. If people with T1D wish to engage in exercise in a safe manner, a certain level of pre-planning before exercise is required in terms of insulin dosing and target glucose concentration. Numerous research projects have been performed in the morning where participants exercise in the fasted state, for logistical reasons, because of easier insulin management in fasting conditions and a lower risk of hypoglycaemia during or after the exercise bout. However, in reality, advanced planning of exercise is not always possible, and many patients may also wish to exercise after their meal. Hence, it is important to take into account the impact of prandial state on blood glucose responses to exercise in patients with T1D. While evidence on the importance of timing of exercise and on the benefits of postprandial exercise for improving glucose control is available in patients with type 2 diabetes, less studies have been conducted in T1D despite this being of high clinical importance. Therefore, more insight is needed into the glycaemic and metabolic effects of different postprandial exercise modalities aiming to reduce the risk of hypoglycaemia and improve glucose control, both during and after exercise. Postprandial exercise can be a useful strategy to improve glycaemic control but research in T1DM is very scarce, with only few studies that have been conducted and optimal exercise regimens remaining unknown. Summarizing, prandial state is an important factor to take into account in exercise in people with T1D, with glycaemic responses that substantially vary between fasted or postprandial exercise. Performing exercise in the postprandial period is of high clinical relevance however there is a scarcity of research in this area. Therefore, more studies that examine the glycaemic and metabolic effects of different modalities of postprandial exercise in people with T1D are needed. All of this aiming to simplify exercise-associated countermeasures and improve (postprandial) glucose control, and thereby reduce barriers to PA in this population.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date November 21, 2022
Est. primary completion date August 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Type 1 diabetes for = 2 years and negative C-peptide (<100pmol/l) - Male and female aged 18-65 years old - HbA1c <9% (at least two values in a row in the past year), based on analysis from the central laboratory unit of Ghent University Hospital. - Insulin treatment: multiple daily injections (MDI) or continuous subcutaneous insulin infusion (CSII): insulin pump alone without connection to sensor, or sensor-augmented pump (SAP) with or without stop at/before low; however no hybrid closed-loop systems will be included). - Able to understand study instructions and to provide written informed consent. Exclusion Criteria: - Physical or psychological disease likely to interfere with the normal conduct of the study as judged by the investigator. - Body mass index >= 35 kg/m2. - Self-monitoring of blood glucose (SBMG) with finger prick - CSII with a hybrid closed-loop insulin pump - Taking any medication that affects heart rate. - Current treatment with drugs known to interfere with metabolism, e.g. systemic corticosteroids, SGLT2 inhibitors, glucagon-like-peptide 1 (GLP-1) receptor agonists, or metformin. - Hypoglycaemic unawareness (Gold score =4) or having experienced any episode of a severe hypoglycaemic event within the last 6 months (i.e. need of third-party assistance). - Known coronary or cerebral artery disease, i.e. history of angina pectoris, myocardial infarction (MI), stroke or any cardiovascular procedure. - Severe non-proliferative and unstable proliferative retinopathy, based on medical record. - Severe diabetic peripheral neuropathy (DPN) or autonomic neuropathy, based on medical record. - Uncontrolled hypertension (>180/100 mmHg). - Pregnant or planning to become pregnant during the study period (females) - Breastfeeding (females).

Study Design


Intervention

Other:
Postprandial exercise of different modalities
Physical exercise performed 60 minutes after a standardized meal, of different modalities (4 different modalities will be examined, as described in the Arms)

Locations

Country Name City State
Belgium Ghent University Hospital Ghent

Sponsors (2)

Lead Sponsor Collaborator
University Hospital, Ghent University Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in blood glucose during exercise Change in BG during exercise, calculated based on the participants' BG at the start of exercise and the last value measured at the end of exercise. (If the exercise is stopped early because of hypoglycaemia, the last exercise glucose value will be used for analysis.) 30 minutes (i.e. during exercise)
Secondary Mean blood glucose during exercise and in the 30 min period after exercise. 180 minutes
Secondary Incremental area under the blood glucose curve (iAUC) during exercise and in the 30 min period after exercise. 180 minutes
Secondary Peak postprandial blood glucose (peak BG) concentration. 120 minutes
Secondary Mean interstitial glucose concentration during the overnight period (12:00 AM - 06:00 AM), and in the 24 hours following exercise. 24 hours
Secondary Incremental area under the interstitial glucose curve during the overnight period (12:00 AM - 06:00 AM), and in the 24 hours following exercise. 24 hours
Secondary Incidence of hypoglycaemia during exercise, in the 30 min period after exercise, up to the late postprandial period (240 minutes after the meal), in the overnight period (12:00 AM - 06:00 AM), and the 24 hours following exercise. 24 hours
Secondary Mean plasma lactate concentration during exercise and in the recovery period after the exercise session. 180 minutes
Secondary Mean plasma free fatty acids concentration during exercise and in the recovery period after the exercise session. 180 minutes
Secondary Mean plasma triglycerides concentration during exercise and in the recovery period after the exercise session. 180 minutes
Secondary Mean plasma insulin concentration during exercise and in the recovery period after the exercise session. 180 minutes
Secondary Plasma insulin area under the curve during exercise and in the recovery period after the exercise session. 180 minutes
Secondary Mean plasma glucagon concentration during exercise and in the recovery period after the exercise session. 180 minutes
Secondary Plasma glucagon area under the curve during exercise and in the recovery period after the exercise session. 180 minutes
Secondary Mean plasma adrenaline concentration during exercise and in the recovery period after the exercise session. 180 minutes
Secondary Plasma adrenaline area under the curve during exercise and in the recovery period after the exercise session. 180 minutes
Secondary Mean plasma noradrenaline concentration during exercise and in the recovery period after the exercise session. 180 minutes
Secondary Plasma noradrenaline area under the curve during exercise and in the recovery period after the exercise session. 180 minutes
Secondary Mean plasma cortisol concentration during exercise and in the recovery period after the exercise session. 180 minutes
Secondary Plasma cortisol area under the curve during exercise and in the recovery period after the exercise session. 180 minutes
Secondary Mean plasma growth hormone concentration during exercise and in the recovery period after the exercise session. 180 minutes
Secondary Plasma growth hormone area under the curve during exercise and in the recovery period after the exercise session. 180 minutes
See also
  Status Clinical Trial Phase
Completed NCT04476472 - Omnipod Horizon™ Automated Glucose Control System Preschool Cohort N/A
Completed NCT03635437 - Evaluation of Safety and Diabetes Status Upon Oral Treatment With GABA in Patients With Longstanding Type-1 Diabetes Phase 1/Phase 2
Completed NCT04909580 - Decision Coaching for Youth and Parents Considering Insulin Delivery Methods for Type 1 Diabetes N/A
Active, not recruiting NCT00679042 - Islet Transplantation in Type 1 Diabetic Patients Using the University of Illinois at Chicago (UIC) Protocol Phase 3
Completed NCT03293082 - Preschool CGM Use and Glucose Variability in Type 1 Diabetes N/A
Completed NCT04016662 - Automated Insulin Delivery in Elderly With Type 1 Diabetes (AIDE T1D) Phase 4
Completed NCT02527265 - Afrezza Safety and Pharmacokinetics Study in Pediatric Patients Phase 2
Completed NCT03738865 - G-Pen Compared to Glucagen Hypokit for Severe Hypoglycemia Rescue in Adults With Type 1 Diabetes Phase 3
Completed NCT03240432 - Wireless Innovation for Seniors With Diabetes Mellitus N/A
Completed NCT03168867 - Effectiveness Trial of an E-Health Intervention To Support Diabetes Care in Minority Youth (3Ms) N/A
Completed NCT03674281 - The VRIF Trial: Hypoglycemia Reduction With Automated-Insulin Delivery System N/A
Completed NCT03669770 - Ultrasound Classification and Grading of Lipohypertrophy and Its Impact on Glucose Variability in Type 1 Diabetes
Recruiting NCT03682640 - Azithromycin Insulin Diet Intervention Trial in Type 1 Diabetes Phase 2
Recruiting NCT04096794 - Chinese Alliance for Type 1 Diabetes Multi-center Collaborative Research
Completed NCT02882737 - The Impact of Subcutaneous Glucagon Before, During and After Exercise a Study in Patients With Type 1 Diabetes Mellitus N/A
Recruiting NCT02745808 - Injectable Collagen Scaffold™ Combined With HUC-MSCs for the Improvement of Erectile Function in Men With Diabetes Phase 1
Completed NCT02562313 - A Trial Investigating the Continuous Subcutaneous Insulin Infusion of a Liquid Formulation of BioChaperone Insulin Lispro in Comparison to Humalog® Phase 1
Completed NCT02596204 - Diabetes Care Transformation: Diabetes Data Registry and Intensive Remote Monitoring N/A
Completed NCT02558491 - Feasibility of a Decision Support System to Reduce Glucose Variability in Subject With T1DM N/A
Withdrawn NCT02518022 - How to be Safe With Alcoholic Drinks in Diabetes N/A