Resistance Exercise Effort for Type 2 Diabetes

N/A

Recruiting

Led By Flavio De Castro Magalhaes, PhD

Research Sponsored by University of New Mexico

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Presence of prediabetes (fasting glycemia between 100 and 125 mg/dL or glycated hemoglobin [A1c] between 5.7 and 6.4%) or T2DM (fasting glycemia 126 mg/dL or above or A1c 6.5% or above)

Age between 18 and 65 years

Must not have

Use of oral contraceptives

Non-English speakers

Timeline

Screening 3 weeks

Treatment Varies

Follow Up before and 5 minutes after the resistance exercise sessions.

Summary

This trial is comparing the effect of different levels of effort during a resistance exercise session on blood glucose levels in people with prediabetes or type 2 diabetes. The trial aims to answer whether high effort

Who is the study for?

This trial is for individuals with prediabetes or type 2 diabetes who are interested in how different levels of effort during resistance exercise affect their blood glucose. Participants should be familiar with the exercises and able to commit to multiple sessions.

What is being tested?

The study tests whether a high-effort or low-effort resistance exercise session can improve blood glucose levels compared to no exercise at all. It also examines participants' enjoyment and discomfort after exercising at different intensities.

What are the potential side effects?

Since this trial involves physical exercise, potential side effects may include muscle soreness, fatigue, and general discomfort associated with exertion. The intensity of these side effects could vary based on the level of effort.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

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I have prediabetes or type 2 diabetes based on my blood sugar or A1c levels.

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I am between 18 and 65 years old.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:

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I am currently using oral contraceptives.

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I do not speak English.

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I have kidney failure.

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My blood pressure is not higher than 160/100 mmHg.

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I have had serious heart problems.

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I need someone legally authorized to make decisions for me.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ for 6 hours during the nocturnal period (12 am - 6 am) of each situation (arm) of the study

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~for 6 hours during the nocturnal period (12 am - 6 am) of each situation (arm) of the study

This trial's timeline: 3 weeks for screening, Varies for treatment, and for 6 hours during the nocturnal period (12 am - 6 am) of each situation (arm) of the study for reporting.