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Status unknownNCT03773731Updated Jan 9, 2019

High Intensity Interval Training in Prediabetes

An interventional study of High intensity interval training (HIIT) and Moderate intensity continuous training (MICT) in Prediabetic State, sponsored by Medical University of Vienna. Status unknown at 1 site in Austria. Open to male participants aged 19 Years to 75 Years. Per ClinicalTrials.gov, last updated 2019-01-09.

Sponsored by Medical University of Vienna · Not applicable, Interventional, and Basic science

The sponsor has not verified this record recently (last verified Jan 2019), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
44
Allocation
Randomized
Ages
19 Years to 75 Years
Sex
Male
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Study summary

This trial investigates if high intensity interval training is more effective than moderate intensity continuous training in suppressing platelet reactivity and hepatic fat content in prediabetic individuals.

Read the detailed description

Background:

The prevalence of type 2 diabetes mellitus (T2DM) is rising dramatically. T2DM represents a major cause for cardiovascular disease -related mortality and morbidity and increasingly burdens healthcare systems. While the fundamental pathomechanism of T2DM is insulin resistance of muscle and adipose tissue, recent studies demonstrate that insulin resistance in T2DM also occurs in platelets. As insulin directly inhibits platelet function, this mechanism might contribute to platelet activation and platelet hyperreactivity, which were in fact detected in diabetic patients. Since (inadvertent) platelet activation is causally linked to the development of atherosclerosis and atherothrombosis, regulation of platelet function is of utmost importance. Exercise training, performed on a regular basis has been shown to reduce morbidity and mortality in sedentary and diseased populations. Furthermore, exercise training improves whole body insulin sensitivity - however, it is currently unclear, if exercise training also affects insulin sensitivity of platelets. Recently, a time-saving interval training protocol has been adapted for T2DM-patients. Since this adapted high intensity interval training (HIIT) needs a fractional time commitment of exercise training according to current guidelines, HIIT possibly represents a promising instrument to increase adherence to exercise and thereby reduce T2DM morbidity.

Aims:

The primary aim of this study is to investigate the effect of 12 weeks of HIIT vs. continuous training (CT) on platelet insulin sensitivity and platelet (hyper)reactivity in prediabetic patients.

Secondary aims are to assess the effect of HIIT and CT on whole body insulin sensitivity and fitness in prediabetic patients as well as on various parameters of platelet function and on the hepatic fat content.

Hypotheses:

Our main hypothesis is that HIIT increases platelet insulin sensitivity and thereby decreases platelet activation/reactivity in patients with prediabetes. Methods: 44 prediabetic (see inclusion criteria) patients will be enrolled in this study. Patients will randomly be assigned to a HIIT group (committed to a supervised training program) or a CT group. After initial examinations (supervised graded exercise test, platelet function tests, oral glucose tolerance test, measurement of the hepatic fat content via FibroScan®), supervised training will be performed over a period of 12 weeks. Tests performed at the beginning of the study will be repeated after the training period.

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Conditions studied

  • Prediabetic State

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In context

Prediabetic State

999 studies on the registry are indexed under Prediabetic State; 238 are open to participants now.

This study's planned enrollment of 44 is below the median of 65 across 844 interventional studies indexed under Prediabetic State.

Browse Prediabetic State studies →

Lead sponsor

Medical University of Vienna is the lead sponsor of 1,076 studies on the registry; 176 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
19 Years to 75 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Inclusion criteria

  • prediabetic (insulin-insensitive) patients
  • either fasting plasma glucose 100- 125 mg/dl or HbA1c 5.7 - 6.4
  • \< 3kg bodyweight change within the last 6 months

Exclusion criteria

Exclusion Criteria:

  • Any contraindications for exercise
  • resulting from anamnesis ( e.g. history of angina pectoris, peripheral arterial disease), ECG at rest or during graded exercise test, echocardiogram, echocardiography or lung function test
  • chronical joint pain that makes exercise training on bicycle ergometers impossible
  • any conditions that make the successful participation in the study unlikely
  • islet cell autoantibodies
  • Medication: insulin, thiazolidindiones, statins, antidepressants
  • Secondary diseases: History of end-stage liver or kidney disease; pronounced neuropathy or retinopathy
  • drug or alcohol abuse
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Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
44 participants (estimated)

Study arms

  • Experimental
    High intensity interval training

    3x/week the following 45 min training protocol on bicycle ergometer for 12 weeks: * 5 minutes warm-up phase with a power output of 40% of the maximal power output achieved in an incremental exercise test * 30 minutes: intensive cycling bouts of 60s interspersed with 60s of recovery intervals. Power output will be 90% (week 1-6) or 95% (week 7-12) of the maximal power output of the exercise test during the intensive cycling bouts. During recovery intervals, subjects will pedal with a power output of 30% (week 1-6) or 35% (week 7-12) of the maximal power output of the exercise test. * 10 minutes with 30% of maximal power output.

    Behavioral: High intensity interval training (HIIT)

  • Active comparator
    Moderate intensity continuous training

    3x/week the following 45 min training protocol on bicycle ergometer for 12 weeks: * 5 minutes warm-up phase with a power output of 40% of the maximal power output achieved in an incremental exercise test * 30 minutes: Continuous training with 60% (week 1-6) or 65% (week 7-12) of maximal power output * 10 minutes with 30% of maximal power output.

    Behavioral: Moderate intensity continuous training (MICT)

Interventions

  • BehavioralHigh intensity interval training (HIIT)

    Exercise training on bicycle ergometer with high intensity bouts of 1 min interspersed by low intensity recovery intervals

  • BehavioralModerate intensity continuous training (MICT)

    Exercise training on bicycle ergometer with moderate intensity (60 - 65 % of individual maximal power output)

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What researchers measure

Primary outcomes

  1. EC50 (half-maximal effective concentration) of TRAP-6 (thrombin-receptor activating peptide) in terms of surface CD62P (=platelet selectin, P-selectin) expression: group differences after 12 weeks of training

    Time frame: 12 weeks

  2. EC50 of insulin in terms of intraplatelet VASP (vasodilator-stimulated phosphoprotein)-phosphorylation: group differences after 12 weeks of training

    Time frame: 12 weeks

Secondary outcomes

  1. whole body insulin sensitivity

    Time frame: 12 weeks

  2. Maximal oxygen consumption

    Unit: ml/min/kg bodymass

    Time frame: 12 weeks

  3. EC50 of other platelet agonists in terms of various platelet activation markers

    Time frame: 12 weeks

  4. EC50 of prostacyclin in terms of intraplatelet VASP-phosphorylation

    Time frame: 12 weeks

  5. Transient elastography (FibroScan®) controlled attenuation parameter (CAP)

    The controlled attenuation parameter (CAP) has demonstrated good accuracy in quantifying the levels of liver steatosis and fibrosis in patients with NAFLD

    Time frame: 12 weeks

  6. Fatty Liver Index (FLI)

    Time frame: 12 weeks

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Study locations

1 of 1 sites recruiting
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 9, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03773731
Lead sponsor
Medical University of Vienna
Collaborators
University of Vienna, Institute for Sport Science, Sanatorium Hera Vienna
Responsible party
Stefan Heber (Dr.med.univ. Dr.rer.nat., Medical University of Vienna) — Principal investigator
First posted
Dec 12, 2018
Start date
Jan 4, 2019
Primary completion
Dec 2020 (estimated)
Completion
Feb 2021 (estimated)
Last update
Jan 9, 2019

Study contacts

Ivo Volf, PhD
Contact
ivo.volf@meduniwien.ac.at
+43 40160 ext. 31421
Rochus Pokan, MD
Contact
rochus.pokan@univie.ac.at
+43 4277 4887225

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Jan 2019. You cannot join it, but the record below documents what was studied.

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