- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02185872
CrossFit Exercise to Improve Glucose Control for Overweight and Obese Adults
March 30, 2015 updated by: Katie M. Heinrich, Kansas State University
The Influence of a CrossFit Exercise Program on Glucose Control in Overweight and Obese Individuals
The purpose of this study was to examine the differences in glucose control, fitness, and body composition between a standard aerobic and resistance exercise training program and a shorter-duration, high-intensity CrossFit training program in overweight and obese physically inactive adults.
Hypotheses:
- Both groups would improve glucose control, with the CrossFit group improving significantly more than the aerobic and resistance training group.
- Both groups would improve fitness, with the CrossFit group improving significantly more than the aerobic and resistance training group.
- Both groups would demonstrate decreases in body fat percentage and fat mass and increases in lean body mass, with the CrossFit group improving significantly more than the aerobic and resistance training group.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Overweight or obese participants will take part in an 8-week exercise intervention after clearance from a doctor, that is expected to improve glucose control, fitness (Eurofit and peak aerobic capacity), and body composition (body fat percentage, fat mass, and lean body mass).
After stratification by age and body mass index, participants will be randomized to either a standard aerobic and resistance training exercise program or a relatively higher intensity, shorter duration CrossFit exercise program.
Study Type
Interventional
Enrollment (Actual)
23
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Kansas
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Manhattan, Kansas, United States, 66506
- Kansas State University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 40 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- body mass index (BMI) of 25 - < 40, physically inactive (i.e., not participating in any structured exercise programs for the past 2 months and not exceeding 30 total minutes of physical activity per week)
Exclusion Criteria:
- current smoker, pregnant, taking blood glucose altering medications, heart disease, type 1 or 2 diabetes mellitus, total cholesterol 200 mg/dL or higher
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Aerobic and Resistance Training
Participants completed 24 exercise sessions based on current guidelines.
Aerobic exercise (50 min) was performed on machines every session and resistance training (20 min) was performed on machines two sessions per week.
Aerobic intensity was prescribed at 40-50% of heart rate reserve (HRR) Weeks 1-4 and 50-60% HRR Weeks 5-8.
Resistance training was supervised by an ACE certified personal trainer.
One-repetition maximums (1-RM) were assessed Week 1 (i.e., seated bicep curl, military press, seated lat pulldown, seated leg extension, triceps pulldown, bench press, reverse leg curl, seated leg press).
For Weeks 2-3 participants completed, 3 sets of 15 reps at 50% 1-RM; Weeks 4-5, 3 sets of 12 reps at 60% 1-RM; Weeks 6-7, 3 sets of 10 reps at 70% 1-RM; Week 8, 3 sets of 8 reps at 75% 1-RM.
Three sets of 15 unweighted crunches were completed each day.
One minute of rest was taken between each set and each exercise.
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The protocol was based upon current guidelines of 150 minutes moderate-intensity aerobic activity and 2 days of muscle strengthening per week.
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Experimental: High-intensity functional training
Participants completed a total of 24 sessions that were pre-programmed and led by a certified instructor (CrossFit Level 2), which lasted up to 60 minutes in duration.
The first two class periods were structured as an introduction to common movements used in high-intensity functional training (HIFT; e.g., squats, deadlift, press, jerks, barbell, dumbbell, and medicine ball cleans, pullups, kettlebell swings, among others).
No scheduled workouts were given on days 1 and 2. Beginning on day 3 each HIFT class consisted of 10-15 minutes of stretching and warmup, 10-20 minutes of instruction and practicing techniques and movements, and 5-30 minutes for the workout of the day, performed at vigorous intensity, relative to each person's ability and fitness level.
All weights and movements were individually prescribed and recorded for each participant.
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Participants were instructed to work as hard as they could while maintaining safe technique and proper form to achieve as many reps or rounds as possible in the prescribed time frame.
As HIFT participants became accustomed to specific movements, less time was dedicated to practicing movements and technique.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from baseline in glucose control.
Time Frame: Baseline, Week 10
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Fasting plasma glucose levels were taken after an overnight fast of at least 8 hours.
An oral glucose tolerance test was conducted after ingestion of a 75g oral dextrose solution with finger sticks at 30, 45, and 60 minutes from time 0. The following equation was used to calculate glucose area under the curve which was the metric utilized to ascertain changes in glucose control: [(Time 45 - Time 30) * ½ (OGTT 30 + OGTT 45)] + [(Time 60 - Time 45) * ½ (OGTT 60 + OGTT 45)]
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Baseline, Week 10
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from baseline in peak aerobic capacity
Time Frame: Baseline, Week 10
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Modified Balke protocol
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Baseline, Week 10
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Change from baseline in sit and reach
Time Frame: Baseline, Week 10
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Eurofit protocol for sit and reach distance using flex tester box
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Baseline, Week 10
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Change from baseline in standing broad jump
Time Frame: Baseline, Week 10
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Eurofit protocol
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Baseline, Week 10
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Change from baseline in vertical jump
Time Frame: Baseline, Week 10
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Eurofit protocol
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Baseline, Week 10
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Change from baseline in pushups
Time Frame: Baseline, Week 10
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Eurofit protocol; completed on feet or knees
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Baseline, Week 10
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Change from baseline in situps
Time Frame: Baseline, Week 10
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Eurofit protocol
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Baseline, Week 10
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Change from baseline in 40 meter dash
Time Frame: Baseline, Week 10
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A handheld stopwatch was used to record time from the command "Go" until the participant crossed the line at 40 meters
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Baseline, Week 10
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Change from baseline in stork balance test
Time Frame: Baseline, Week 10
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Baseline, Week 10
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Change from baseline in body composition
Time Frame: Baseline, Week 12
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Dual X-ray absorptiometry scan was used to assess body fat percentage, lean body mass, and fat mass.
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Baseline, Week 12
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Time spent completing daily workouts
Time Frame: 24 exercise sessions over 8 weeks
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Time spent to complete each assigned daily workout was individually recorded for each participant
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24 exercise sessions over 8 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Katie M Heinrich, PhD, Kansas State University
- Study Director: Pratik Patel, MS, RD, Kansas State University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2012
Primary Completion (Actual)
May 1, 2012
Study Completion (Actual)
May 1, 2012
Study Registration Dates
First Submitted
July 3, 2014
First Submitted That Met QC Criteria
July 9, 2014
First Posted (Estimate)
July 10, 2014
Study Record Updates
Last Update Posted (Estimate)
March 31, 2015
Last Update Submitted That Met QC Criteria
March 30, 2015
Last Verified
March 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- #6058
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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