ClinicalTrials.gg
RecruitingNCT06993454ACELERATE-PUpdated Aug 12, 2026

Acute Exercise and Endogenous Glucose Production in Type 2 Diabetes: Implications for Glycemic Control and Treatment of Hepatic Steatosis

An interventional study of Magnetic Resonance Liver Assessment and Bike Exercise VO2max in Type 2 Diabetes and Hepatic Steatosis, sponsored by AdventHealth Translational Research Institute. Recruiting at 1 site in United States. Open to participants aged 25 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-12.

Sponsored by AdventHealth Translational Research Institute · Not applicable, Interventional, and Other

From the registry’s dates

  • Started Apr 2025; still recruiting 1 year 6 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
12
Allocation
Non-randomized
Ages
25 Years to 55 Years
Sex
All
01

Study summary

The overall aim of this study is to investigate the effects of exercise on the amount of glucose that is made by the liver in people with and without Type 2 diabetes (T2D) and hepatic steatosis (fatty liver).

02

Conditions studied

  • Type 2 Diabetes
  • Hepatic Steatosis
03

In context

Diabetes Mellitus, Type 2

10,371 studies on the registry are indexed under Diabetes Mellitus, Type 2; 1,406 are open to participants now.

This study's planned enrollment of 12 is below the median of 80 across 8,350 interventional studies indexed under Diabetes Mellitus, Type 2.

Browse Diabetes Mellitus, Type 2 studies →

Lead sponsor

AdventHealth Translational Research Institute is the lead sponsor of 57 studies on the registry; 11 are open to participants now.

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

04

Who can participate

Ages eligible
25 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion criteria for individuals with T2D and elevated liver fat ≥5.6%

  1. Provision of signed and dated form
  2. Stated willingness to comply with all study procedures and availability for the duration of the study
  3. Male or (pre-menopausal) female, aged 25-55 years
  4. (BMI) between 25 and 45 kg/m2
  5. Sedentary (1 day or less per week of structured exercise)
  6. Type 2 diabetes mellitus: ≥7.5%
  7. Liver fat ≥5.6% based on MRI
  8. Weight stable (± 2 kg) for prior 3 months

Inclusion criteria for lean, healthy controls

  1. Provision of signed and dated informed consent form
  2. Stated willingness to comply with all study procedures and availability for the duration of the study
  3. Male or (pre-menopausal) female, aged 25-55 years
  4. Body mass index (BMI) between 18.5 and 27.5 kg/m2
  5. Normal liver fat (FibroScan CAP \<249dB/m, \<5.6% liver fat based on MRI)
  6. Weight stable (± 2 kg) for prior 3 months
  7. Active (≥3 day/week of structured exercise)

Exclusion Criteria

  1. Exclusion criteria for individuals with T2D and elevated liver fat ≥5.6% Currently taking insulin, incretin mimetics, and/or thiazolidinediones
  2. Any change in glucose-lowering medications within the previous three months.
  3. Inability to stop any medications which interfere with glucose metabolism for visits 4 and 7.
  4. Resting blood pressure ≥ 160/100 mm Hg
  5. Triglycerides ≥ 500 mg/dL
  6. Any renal, cardiac, liver, lung, or neurological disease that in the opinion of the principal investigator would compromise participant safety or the participants' ability to complete the exercise protocol
  7. Any significant disease or unstable medical condition (i.e., coronary heart disease, chronic renal failure, chronic hepatic disease, severe pulmonary disease)
  8. Presence of abnormalities on (ECG) that is a to exercise testing
  9. Cancer (active with or without concurrent chemotherapy; except for basal cell carcinoma)
  10. Pregnancy during the previous 6 months, lactating, or planned pregnancy in the next 6 months
  11. Post- or peri-menopausal women
  12. Partial and/or full hysterectomy (self-report)
  13. Use of drugs known to affect energy metabolism or body weight: including, but not limited to orlistat, sibutramine, ephedrine, phenylpropanolamine, corticosterone, etc
  14. Hyperthyroidism including those with normal TSH (0.35-4.5) on pharmacological treatment; individuals with hypothyroidism may be referred to their primary care provider for evaluation and retested; any medication change for hypothyroidism must be stable for ≥3 months prior to retesting
  15. Current treatment with blood thinners or anti- medications that cannot be safely stopped for testing procedures
  16. New onset (\<3 months on a stable regime) hormone replacement therapy
  17. Current use of beta-adrenergic blocking agents
  18. Major surgery on the abdomen, pelvis, or lower extremities within previous 3 months
  19. Previous bariatric or other surgery for obesity
  20. Abnormal blood count/anemia ( \<12 g/dl in men or 11 g/dl in women; Hct \<34%), blood transfusion or blood donation within the last 2 months
  21. Current smokers (smoking within the past 3 months prior to screening visit, including any/all tobacco products)
  22. Current drug or alcohol abuse/dependence, or positive urine toxicology screen
  23. Alcohol consumption >7 drinks per week for women or 14 drinks per week for men or history of binge drinking (≥5 drinks for males or 4 drinks for females in a 2-hour period more than once per month)
  24. Metal implants (pacemaker, aneurysm clips) based on investigator's judgment at screening
  25. Not physically capable of performing the exercise required of the study protocols
  26. Unable to participate in Magnetic Resonance Imaging (MRI) assessments due to physical limitations of equipment tolerances (e.g. MRI bore size) based on investigator's judgment at screening.
  27. Unable to tolerate MRI or claustrophobia.
  28. Diagnosed psychotic or psychiatric conditions prohibiting adherence to study protocol; hospitalization for any psychotic or psychiatric condition within one year
  29. Self-reported chronic, active, or latent infection requiring chronic antibiotic or anti-viral treatment; (HIV); active or C undergoing antiviral therapy
  30. Unable or unwilling to communicate with staff or to provide written informed consent

Exclusion criteria for lean, healthy controls

  1. Currently taking insulin, injectable incretin mimetics, and/or thiazolidinediones
  2. Taking glucose-lowering medications
  3. HbA1c ≥ 5.7%; pre-diabetes, type 2 diabetes, or type 1 diabetes
  4. Resting blood pressure ≥ 160/100 mm Hg
  5. Triglycerides ≥ 500 mg/dL
  6. Any renal, cardiac, liver, lung, or neurological disease that in the opinion of the principal investigator would compromise participant safety or the participants' ability to complete the exercise protocol
  7. Any significant disease or unstable medical condition (i.e., coronary heart disease, chronic renal failure, chronic hepatic disease, severe pulmonary disease)
  8. Presence of clinically significant abnormalities on electrocardiogram (ECG) that is a contra-indication to exercise testing
  9. Cancer (active malignancy with or without concurrent chemotherapy; except for basal cell carcinoma)
  10. Pregnancy during the previous 6 months, lactating, or planned pregnancy in the next year
  11. Post- or peri-menopausal women
  12. Partial and/or full hysterectomy (self-report)
  13. Use of drugs known to affect energy metabolism or body weight: including, but not limited to orlistat, sibutramine, ephedrine, phenylpropanolamine, corticosterone, etc
  14. Hyperthyroidism including those with normal TSH (0.35-4.5) on pharmacological treatment; individuals with hypothyroidism may be referred to their primary care provider for evaluation and retested; any medication change for hypothyroidism must be stable for ≥3 months prior to retesting
  15. Current treatment with blood thinners or anti-platelet medications that cannot be safely stopped for testing procedures
  16. New onset (\<3 months on a stable regime) hormone replacement therapy
  17. Current use of beta-adrenergic blocking agents
  18. Major surgery on the abdomen, pelvis, or lower extremities within previous 3 months
  19. Previous bariatric or other surgery for obesity
  20. Increased liver function tests (/ALT/GGT/or alkaline phosphatase greater than 2.5 times the )
  21. Abnormal blood count/anemia (hemoglobin \<12 g/dl in men or 11 g/dl in women; Hct \<34%), blood transfusion or blood donation within the last 2 months
  22. Current smokers (smoking within the past 3 months prior to screening visit, including any/all tobacco products)
  23. Current drug or alcohol abuse/dependence, or positive urine toxicology screen
  24. Alcohol consumption >7 drinks per week for women or 14 drinks per week for men or history of binge drinking (≥5 drinks for males or 4 drinks for females in a 2-hour period more than once per month)
  25. Metal implants (pacemaker, aneurysm clips) based on investigator's judgment at screening
  26. Not physically capable of performing the exercise required of the study protocols
  27. Unable to participate in Magnetic Resonance Imaging (MRI) assessments due to physical limitations of equipment tolerances (e.g. MRI bore size) based on investigator's judgment at screening.
  28. Unable to tolerate MRI or claustrophobia.
  29. Diagnosed psychotic or psychiatric conditions prohibiting adherence to study protocol; hospitalization for any psychotic or psychiatric condition within one year
  30. Self-reported chronic, active, or latent infection requiring chronic antibiotic or anti-viral treatment; Human Immunodeficiency Virus (HIV); active hepatitis B or C undergoing antiviral therapy
  31. Unable or unwilling to communicate with staff or to provide written informed consent
Terms in these criteria, in plain language(13)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

HbA1c

A blood test of average blood sugar over the past two to three months, given as a percentage or in mmol/mol. 6.5% (48 mmol/mol) or more is the usual threshold for diabetes, normally confirmed by a second test.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
12 participants (estimated)

Study arms

  • Other
    Lean, healthy controls

    Control group.

    Other: Magnetic Resonance Liver Assessment · Other: Bike Exercise VO2max · Other: DEXA

  • Other
    Individuals with T2D and hepatic steatosis

    T2D group.

    Other: Magnetic Resonance Liver Assessment · Other: Bike Exercise VO2max · Other: DEXA

Interventions

  • OtherMagnetic Resonance Liver Assessment

    Liver fat will be measured by MR imaging to assess level of hepatic steatosis.

  • OtherBike Exercise VO2max

    Maximal fitness measured by cycle ergometer.

  • OtherDEXA

    Measure body composition (fat and lean body mass).

06

What researchers measure

Primary outcomes

  1. Measurement of Endogenous Glucose Production (EGP)

    Bulk EGP will be measured during resting and exercise conditions to determine how Endogenous Glucose Production (EGP) differs during exercise (compared to no exercise) in T2D and Metabolic dysfunction associated steatotic liver disease (MASLD).

    Time frame: Day 14

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Apr 2025 (actual). Primary completion is estimated for Dec 2028, 44 months after the start.

Of 2,066 non-industry interventional studies with no phase under Diabetes Mellitus, Type 2, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 40. This study's planned 44 months is above that.

Counting every sponsor, half of 2,243 studies reached it within 21 months; a quarter within 10 and three quarters within 39.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 11, 2025
First posted
May 28, 2025
StartActual
Apr 25, 2025
Primary completionEst.
Dec 2028
CompletionEst.
Dec 2028
Last update
Aug 12, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06993454
Lead sponsor
AdventHealth Translational Research Institute
Responsible party
Sponsor
First posted
May 28, 2025
Start date
Apr 25, 2025
Primary completion
Dec 2028 (estimated)
Completion
Dec 2028 (estimated)
Last update
Aug 12, 2026

Study contacts

Recruitment Department
Contact
CFD.TRI.Recruitment@AdventHealth.com
407-303-7100
Justine Mucinski, PhD
principal investigator · AdventHealth

Oversight

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

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