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Resistance Training for Type 1 Diabetes
N/A
Recruiting
Research Sponsored by University of Louisville
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Actively utilizing continuous glucose monitoring for diabetes management
≥ 13 years of age
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 months
Awards & highlights
No Placebo-Only Group
Summary
This trial looks at how different resistance training programs can help regulate blood sugar in young athletes with Type 1 Diabetes Mellitus.
Who is the study for?
This trial is for young athletes who have had Type 1 Diabetes (T1DM) for at least two years, use continuous glucose monitoring, and are familiar with strength training. They must be over 13 years old and have an HbA1C level of 10% or lower. It's not suitable for those with physical limitations that affect exercise or non-English speakers.
What is being tested?
The study is examining how different resistance training programs impact blood sugar control in individuals with T1DM. Participants will engage in various strength-training exercises to see which regimen might be most beneficial.
What are the potential side effects?
While the trial itself does not involve medication and thus has no direct side effects like drugs do, participants may experience typical exercise-related discomforts such as muscle soreness or fatigue.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I use a continuous glucose monitor for my diabetes.
Select...
I am 13 years old or older.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Assess glucose response to different resistance training methods
Secondary study objectives
To assess for correlation between lactate and glucose using different resistance training methods
Side effects data
From 2010 Phase 2 trial • 167 Patients • NCT0011215166%
Other noncardiovascular serious adverse events
13%
Other nonserious adverse events
11%
Persistently elevated PSA
4%
Total serious cardiovascular adverse events
4%
Persistently elevated HCT >= 54%
2%
Elevated AUA
100%
80%
60%
40%
20%
0%
Study treatment Arm
Placebo
Lower-range T
Higher-range T
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Resistance TrainingExperimental Treatment1 Intervention
Bench press, Deadlift, Seated overhead press machine
Find a Location
Who is running the clinical trial?
University of LouisvilleLead Sponsor
348 Previous Clinical Trials
77,363 Total Patients Enrolled
Norton HealthcareOTHER
16 Previous Clinical Trials
2,846 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I use a continuous glucose monitor for my diabetes.Your HbA1C level is less than or equal to 10%.I am 13 years old or older.You have previously participated in strength and conditioning exercises.I was diagnosed with type 1 diabetes over 2 years ago.I have a physical condition that might stop me from completing study tasks.
Research Study Groups:
This trial has the following groups:- Group 1: Resistance Training
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.