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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03544684
Other study ID # T1D_PARTA
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 9, 2015
Est. completion date October 10, 2017

Study information

Verified date June 2018
Source Liverpool John Moores University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to compare the effect of a bout of high-intensity interval training (HIT) with a bout of moderate-intensity continuous training (MICT) on glucose concentrations over the subsequent 24h period.


Description:

This study aims to compare the effect of a bout of high-intensity interval training (HIT) with a bout of moderate-intensity continuous training (MICT) on glucose concentrations over the subsequent 24h period. Fourteen people with type 1 diabetes (duration of type 1 diabetes 8.2±1.4 years), all on basal-bolus regimen, completed a randomised, counterbalanced, crossover study. Continuous glucose monitoring was used to assess glycaemic control following a single bout of HIT (6 x 1min intervals) and 30 mins of moderate-intensity continuous training (MICT) on separate days, compared to a non-exercise control day (CON). Exercise was undertaken following an overnight fast with omission of short-acting insulin. Capillary blood glucose samples were recorded pre and post-exercise to assess the acute changes in glycaemia during HIT and MICT.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date October 10, 2017
Est. primary completion date October 10, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 55 Years
Eligibility 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 and

- unstable proliferative retinopathy

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Effects of the type of exercise on blood glucose concentrations
glucose concentrations were assessed over the 24 hour periods following no exercise, a single bout of high intensity interval training and a single bout of moderate intensity continuous training

Locations

Country Name City State
United Kingdom Liverpool John Moores University Liverpool Merseyside

Sponsors (1)

Lead Sponsor Collaborator
Liverpool John Moores University

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary 24 hour glycaemic profile Continuous glucose monitoring will be used to assess the effects of an acute bout of fasted high intensity interval training or moderate intensity continuous training on 24 hour glycaemic profile. 24 hours
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