Actively Recruiting

Phase Not Applicable
Age: 30Years - 75Years
All Genders
NCT06382246

The Acute Effect of "Exercise Snacks" on Glycemic Responses in Individuals With Type 2 Diabetes.

Led by University of British Columbia · Updated on 2024-05-08

30

Participants Needed

1

Research Sites

64 weeks

Total Duration

On this page

Sponsors

U

University of British Columbia

Lead Sponsor

M

McMaster University

Collaborating Sponsor

AI-Summary

What this Trial Is About

To conduct a randomized crossover trial to determine the acute impact of exercise snacks on glycemic control in physically inactive individuals living with type 2 diabetes using continuous glucose monitoring.

CONDITIONS

Official Title

The Acute Effect of "Exercise Snacks" on Glycemic Responses in Individuals With Type 2 Diabetes.

Who Can Participate

Age: 30Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 30-75 years old.
  • Physician-diagnosed type 2 diabetes.
  • Currently participating in less than 150 minutes of moderate-to-vigorous intensity aerobic exercise per week.
  • Body mass index between 18.5 and 40 kg/m2.
  • Stable medication dosage with no changes for at least 6 months.
  • Able to maintain current medication doses during the study.
  • Able to maintain current physical activity patterns during the study.
  • HbA1c less than or equal to 8.5%.
  • Access to a computer, tablet, or smartphone for intervention delivery and tracking.
  • Can travel to McMaster University for laboratory visits.
  • Can read, write, and understand English.
  • Anticipate having internet access for the next 3-4 months.
  • Cleared for exercise participation based on the CSEP Get Active Questionnaire and the Rose Angina Questionnaire.
Not Eligible

You will not qualify if you...

  • Taking 4 or more glucose-lowering medications.
  • Taking insulin.
  • Taking beta-blockers.
  • Taking 3 or more medications for cardiovascular disease prevention.
  • Had severe hypoglycemia in the past 6 months.
  • Currently a cigarette smoker.
  • Have a chronic musculoskeletal condition preventing exercise.
  • Had a recent cardiovascular event within 2 years preventing exercise.
  • Experience angina upon exertion.
  • Have uncontrolled high blood pressure or abnormal pulse at rest or during exercise.
  • Scheduled for surgery in the next 3-4 months preventing exercise.
  • Diagnosed with cardiac or pulmonary diseases preventing exercise.
  • Have a psychiatric disorder preventing study completion.
  • Donated more than 0.5 L of blood in the last 4 weeks.
  • Following an extreme diet or taking supplements affecting glucose control.
  • Have diabetic ulcers, peripheral vascular disease, or neuropathy preventing exercise.
  • Currently on dialysis.
  • Participating in another interfering clinical trial.
  • Currently pregnant or planning pregnancy during the intervention.

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of British Columbia Okanagan

Kelowna, British Columbia, Canada, V1V 3G1

Actively Recruiting

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Research Team

J

Jonathan P Little, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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