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Clinical Trials/NCT03545841
NCT03545841
Completed
N/A

High-Intensity Interval Training Improves Aerobic Capacity and Abolishes the Decline in Blood Glucose Observed During Moderate-Intensity Continuous Training Sessions in People With Type 1 Diabetes

Liverpool John Moores University1 site in 1 country14 target enrollmentMarch 9, 2015
ConditionsType1diabetes

Overview

Phase
N/A
Intervention
Not specified
Conditions
Type1diabetes
Sponsor
Liverpool John Moores University
Enrollment
14
Locations
1
Primary Endpoint
Maximal aerobic capacity
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Few people with type 1 diabetes achieve exercise guidelines and many programmes designed to increase physical activity have failed. High-intensity interval training (HIT) has been shown to be a time-efficient alternative to traditional moderate-intensity continuous training (MICT) in various groups without type 1 diabetes. A single bout of HIT does not increase the risk of hypoglycaemia in people with type 1 diabetes. This study aimed to assess whether HIT a safe, effective and time-efficient training strategy to improve cardio-metabolic health and reduce the risk of hypoglycaemia in people with type 1 diabetes.

Detailed Description

This study aimed to investigate whether 1) six weeks of high-intensity interval training (HIT) induces similar improvements in cardio-metabolic health markers as moderate-intensity continuous training (MICT) in people with type 1 diabetes, and 2) whether HIT abolishes acute reductions in plasma glucose observed following MICT sessions. Fourteen sedentary individuals with type 1 diabetes (n=7 per group) completed six weeks of HIT or MICT 3 times per week. Pre- and post-training measurements were made of 24h interstitial glucose profiles (using continuous glucose monitors (CGMS)) and cardio-metabolic health markers (V ̇O2peak, blood lipid profile and aortic pulse wave velocity; aPWV). Capillary blood glucose concentrations were assessed before and after exercise sessions throughout the training programme to investigate changes in blood glucose during exercise in the fed state.

Registry
clinicaltrials.gov
Start Date
March 9, 2015
End Date
October 10, 2017
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sam Shepherd

Dr Sam Shepherd, Principle Investigator

Liverpool John Moores University

Eligibility Criteria

Inclusion Criteria

  • duration of type 1 diabetes \>6 months
  • basal bolus regimen
  • no significant history of hyper- or hypoglycaemia (determined from medical history)

Exclusion Criteria

  • duration of type 1 diabetes \<6 months,
  • insulin pump therapy
  • significant history of hyper- or hypoglycaemia (determined from medical history)
  • obesity (BMI \>30 kg∙m-2)
  • pregnancy or planning pregnancy
  • uncontrolled hypertension (\>180/100 mmHg)
  • angina, autonomic neuropathy
  • taking any medication that affects heart rate
  • major surgery planned within 6 weeks of the study
  • severe nonproliferative

Outcomes

Primary Outcomes

Maximal aerobic capacity

Time Frame: change in baseline maximal aerobic capacity at 6 weeks

Maximal aerobic capacity test pre and post 6-week training intervention

Secondary Outcomes

  • Vascular stiffness(change in baseline vascular stiffness at 6 weeks)

Study Sites (1)

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