ClinicalTrials.Veeva

Menu

Type 2 Diabetes Post Exercise Arterial Stiffness

University of Illinois logo

University of Illinois

Status

Withdrawn

Conditions

Type 2 Diabetes

Treatments

Other: Exercise Test

Study type

Interventional

Funder types

Other

Identifiers

NCT06438874
STUDY2024-0610

Details and patient eligibility

About

The overall aim of this research proposal is to determine the impact of GLP1 agonists on post-exercise arterial stiffness. Therefore, the investigators will examine the cardiovascular responses to exercise in individuals with Type 2 Diabetes mellitus (T2DM) taking these medications during and following a graded maximal exercise test.

Full description

Type 2 diabetes mellitus (T2DM) is a significant public health concern associated with increased cardiovascular morbidity and mortality. Notably, individuals with T2DM often exhibit increased arterial stiffness, a key indicator of cardiovascular risk. Pharmacological interventions such as GLP1 agonists have emerged as crucial treatments for T2DM, offering glycemic control and potential cardiovascular benefits, including improvements in blood pressure and arterial stiffness. However, while the effects of GLP1 agonists on glycemic control and blood pressure regulation have been explored, their impact on arterial stiffness, specifically in response to exercise, remains largely unexplored in individuals with T2DM. Arterial stiffness is a critical marker of cardiovascular health, and its reduction is associated with decreased cardiovascular risk which include lowered blood pressure. Therefore, the overall aim of this research is to investigate whether GLP1 agonists attenuate arterial stiffness post exercise and reduce peak exercise blood pressure in individuals with T2DM.

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Individuals diagnosed with type 2 diabetes mellitus (T2DM).

  • Age between 18 and 60 years old.
  • Currently receiving treatment with a glucagon-like peptide 1 (GLP1) agonist for the management of T2DM for a minimum duration of six months.
  • For control group no current use of a glucagon-like peptide 1 (GLP1) agonist for the management of type 2 diabetes mellitus (T2DM).
  • HbA1c levels between 6.5-8%
  • Body Mass Index (BMI) within the range of 25 to 40 kg/m2.

Exclusion criteria

  • Coronary heart disease.
  • Pulmonary disease (e.g. asthma, chronic obstructive pulmonary disease)
  • Neurological disorders (e.g. Alzheimer's disease, dementia)
  • Congestive heart failure.
  • Peripheral vascular disease.
  • Liver failure.
  • Kidney failure.
  • Alcohol abuse.
  • Drug abuse.
  • Smoking.
  • Hypertension (defined as Systolic Blood Pressure ≥ 140 mmHg or Diastolic Blood Pressure ≥ 90 mmHg)
  • Insulin therapy for the management of T2DM
  • Severe obesity (defined as Body Mass Index >40 kg/m2);
  • Pregnancy
  • Non-English speaking individuals

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

GLP-1 Treatment
Experimental group
Description:
Individuals diagnosed with type 2 diabetes mellitus (T2DM) who are currently receiving treatment with a glucagon-like peptide 1 (GLP1) agonist.
Treatment:
Other: Exercise Test

Trial contacts and locations

0

Loading...

Central trial contact

Philip Clifford, PhD; Ronald E Jackson, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems