A Comparison of High-intensity Interval Training Protocols on Health and Fitness
1 other identifier
interventional
16
1 country
1
Brief Summary
Recently, it has been demonstrated that multimodal high-intensity interval training (MM-HIIT) (utilizing resistance-based and functional movements) can produce similar aerobic adaptations compared to high-intensity interval training (HIIT) using rowing but with greater muscle performance in females. In addition, HIIT has been shown to be more enjoyable than continuous training, and this may lead to enhanced self-efficacy and increased physical activity. To the investigators' knowledge, however, the cardiometabolic effects (blood pressure, abdominal/visceral fat, blood sugar, blood lipids/fats) of MM-HIIT have not been reported. The investigators aim to compare MM-HIIT with HIIT using a traditional aerobic fitness exercise (rowing) for the degree of cardiometabolic, physical performance (strength, endurance, power), and psychosocial (self-efficacy and enjoyment) adaptations. They will also determined sustained effects of the intervention by completing a 9-month follow-up.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable healthy
Started Jul 2017
Typical duration for not_applicable healthy
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
First Submitted
Initial submission to the registry
March 17, 2017
CompletedFirst Posted
Study publicly available on registry
March 28, 2017
CompletedStudy Start
First participant enrolled
July 17, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 23, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
August 23, 2018
CompletedMarch 13, 2019
March 1, 2019
1.1 years
March 17, 2017
March 11, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Aerobic fitness
Aerobic fitness will be directly assessed by a VO2max bicycle test. Each participant will be allowed to warm-up on the bicycle for 5 minutes at a low intensity. The VO2max bicycle test will include 3 minute stages with increasing intensity each stage of 30 - 60 watts. The required cadence will be maintained at 60 RPMs (revolutions per minute) for each stage. The test will be terminated at volitional fatigue defined as the participant no longer able to maintain 60 RPMs for 20 seconds after encouragement from the testers. For most people, the test will take approximately 10 minutes.
15 minutes
Secondary Outcomes (2)
Triglycerides
10 minutes
Physical Activity Enjoyment scale
5 minutes
Other Outcomes (17)
Muscular Endurance
5 minutes
Total Cholesterol
5 minutes
Visceral Fat
5 minutes
- +14 more other outcomes
Study Arms (3)
Multimodal
EXPERIMENTALMultimodal High-Intensity Interval Training Intervention. This group will train using multimodal exercises for 5 sets of 60 seconds of all out work, followed by 3 minutes of rest. Each session will have the same exercises within each set, but every session will be different than the others for movements utilized. There will be three movements used in each set. The first movement will be a strength movement for 4-6 repetitions. The second movement follows the first immediately and is a faster body weight or light implement power movement for 6-8 repetitions. The third movement follows the second immediately and is a very fast, sprint-like movement for the remainder of the 60 seconds. The intent of each set is to be completed with as much effort as possible across the full 60 seconds.
Rowing
ACTIVE COMPARATORMultimodal High-Intensity Interval Training Intervention. This group will train using a rowing ergometer for 5 sets of 60 seconds of all out work, followed by 3 minutes of rest (a total of 20 minutes each session). Each training session will be the same across the 12 weeks. The intent of each set is to be completed with as much effort as possible across the full 60 seconds.
Control
NO INTERVENTIONMultimodal High-Intensity Interval Training Intervention. This group will be instructed to continue with any activity they were involved in prior to the study and to not begin any new exercise programs during the course of the study. To incentive participation in this group, the control group will be offered the MM-HIIT intervention the following semester at no cost.
Interventions
The intervention will occur 3 times per week for 12 weeks and include a warm-up, MM-HIIT or R-HIIT training protocol, and a cool down.
Eligibility Criteria
You may qualify if:
- Potential participants will be non-obese (waist circumference ≤ 88 cm) recreationally active females aged 18 - 40 years who do not engage in a regular training program. Recreationally active is defined as periodically participating in physical activity or exercise between 1 - 3 hours a week for at least a month, but not involved in a systematic endurance or weight training activity.
You may not qualify if:
- Potential participants will be excluded if they have a history of exercise-limiting cardiovascular, respiratory, metabolic, or musculoskeletal illness/injury or if they are currently taking medication that would alter the physiological responses to exercise. They will also be excluded if they are pregnant or have a history of fainting while giving blood.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Oakland University
Rochester, Michigan, 48309, United States
Related Publications (1)
Rengers TA, Orr SC, Marks CRC, Hew-Butler T, Choi MD, Butcher SJ, Drignei D, Brown EC. Effects of High-Intensity Interval Training Protocols on Liver Enzymes and Wellness in Women. J Sports Med (Hindawi Publ Corp). 2021 Apr 30;2021:5554597. doi: 10.1155/2021/5554597. eCollection 2021.
PMID: 34007845DERIVED
Study Officials
- PRINCIPAL INVESTIGATOR
Elise Brown, PhD
Oakland University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
March 17, 2017
First Posted
March 28, 2017
Study Start
July 17, 2017
Primary Completion
August 23, 2018
Study Completion
August 23, 2018
Last Updated
March 13, 2019
Record last verified: 2019-03
Data Sharing
- IPD Sharing
- Will not share