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HIT in People With Type 1 Diabetes

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03545841
Enrollment
14
Registered
2018-06-04
Start date
2015-03-09
Completion date
2017-10-10
Last updated
2018-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type1diabetes

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.

Interventions

OTHERHIT

Participants completed 6 weeks of HIT

OTHERMICT

Participants completed 6 weeks of MICT

Sponsors

Liverpool John Moores University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Healthy volunteers
No

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 * unstable proliferative retinopathy

Design outcomes

Primary

MeasureTime frameDescription
Maximal aerobic capacitychange in baseline maximal aerobic capacity at 6 weeksMaximal aerobic capacity test pre and post 6-week training intervention

Secondary

MeasureTime frameDescription
Vascular stiffnesschange in baseline vascular stiffness at 6 weeksAortic pulse wave velocity to measure vascular stiffness

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026