CrossFit Exercise to Improve Glucose Control for Overweight and Obese Adults
The Influence of a CrossFit Exercise Program on Glucose Control in Overweight and Obese Individuals
1 other identifier
interventional
23
1 country
1
Brief Summary
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:
- 1.Both groups would improve glucose control, with the CrossFit group improving significantly more than the aerobic and resistance training group.
- 2.Both groups would improve fitness, with the CrossFit group improving significantly more than the aerobic and resistance training group.
- 3.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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2012
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2012
CompletedFirst Submitted
Initial submission to the registry
July 3, 2014
CompletedFirst Posted
Study publicly available on registry
July 10, 2014
CompletedMarch 31, 2015
March 1, 2015
3 months
July 3, 2014
March 30, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change from baseline in glucose control.
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: \[(Time 45 - Time 30) \* ½ (OGTT 30 + OGTT 45)\] + \[(Time 60 - Time 45) \* ½ (OGTT 60 + OGTT 45)\]
Baseline, Week 10
Secondary Outcomes (9)
Change from baseline in peak aerobic capacity
Baseline, Week 10
Change from baseline in sit and reach
Baseline, Week 10
Change from baseline in standing broad jump
Baseline, Week 10
Change from baseline in vertical jump
Baseline, Week 10
Change from baseline in pushups
Baseline, Week 10
- +4 more secondary outcomes
Other Outcomes (1)
Time spent completing daily workouts
24 exercise sessions over 8 weeks
Study Arms (2)
Aerobic and Resistance Training
ACTIVE COMPARATORParticipants 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.
High-intensity functional training
EXPERIMENTALParticipants 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.
Interventions
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.
The protocol was based upon current guidelines of 150 minutes moderate-intensity aerobic activity and 2 days of muscle strengthening per week.
Eligibility Criteria
You may qualify if:
- 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)
You may not qualify if:
- current smoker, pregnant, taking blood glucose altering medications, heart disease, type 1 or 2 diabetes mellitus, total cholesterol 200 mg/dL or higher
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Kansas State University
Manhattan, Kansas, 66506, United States
Related Publications (1)
Heinrich KM, Patel PM, O'Neal JL, Heinrich BS. High-intensity compared to moderate-intensity training for exercise initiation, enjoyment, adherence, and intentions: an intervention study. BMC Public Health. 2014 Aug 3;14:789. doi: 10.1186/1471-2458-14-789.
PMID: 25086646RESULT
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Katie M Heinrich, PhD
Kansas State University
- STUDY DIRECTOR
Pratik Patel, MS, RD
Kansas State University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
July 3, 2014
First Posted
July 10, 2014
Study Start
February 1, 2012
Primary Completion
May 1, 2012
Study Completion
May 1, 2012
Last Updated
March 31, 2015
Record last verified: 2015-03