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HealthyNCT05821504

High-Intensity Interval Training and Performance

A study testing High-Intensity Interval Training in people with Healthy, run by Kennesaw State University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this clinical trial was to compare to different types of high-intensity interval training in young, healthy females. The main questions were: Will changes in body composition differ between the two interventions? Will changes in endurance and muscle performance differ between the two interventions?… Read more about this study

Who is it for?
Ages 18 to 35 years, women onlyHealthy volunteers can take part
Conditions the study is for
Healthy
What is being tested?
High-Intensity Interval Training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteUnited States
Study dates
1 Aug 2018to 21 Nov 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 35 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Between 18-35 years of age
  • Female
  • Currently participating in 2-4 days of structured exercise for 30-75 minutes for the last 6 months

Who cannot join

  • Currently participating in these exercise formats (2x/week within last 3 months)
  • Engaging in high intensity interval training for more than 30 min/week
  • Have diagnosed disorders/diseases in the following: cardiovascular, pulmonary, immunological, or metabolic
  • Current musculoskeletal injuries
  • Pregnant or think you may be pregnant
  • Currently taking any non-steroidal anti-inflammatory drug(s) or steroidal drug(s)
Show all 10Show fewer
  • Currently a smoker or has consistently smoked within the last year
  • Has a positive written or verbal pre-study drug screen including alcohol (more than 7 drinks/week), THC/cannabinoids, amphetamines, benzodiazepines, cocaine, opioids, phencyclidine, barbiturates, cotinine.
  • Currently taking any medication that will significantly affect your heart rate response to exercise
  • If you miss four or more classes, you will be excluded from the study

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Kennesaw State University

    Kennesaw, Georgia, 30144

Other trials in United States

About this study

Official title: Effects of Plyometric- and Cycle-Based High-Intensity Interval Training on Body Composition, Aerobic Capacity, and Muscle Function in Young Females: a Field-based Group Fitness Assessment

The goal of this clinical trial was to compare to different types of high-intensity interval training in young, healthy females. The main questions were: Will changes in body composition differ between the two interventions? Will changes in endurance and muscle performance differ between the two interventions? Participants were randomized to 8 weeks of high-intensity interval training involving body weight, plyometric exercises or cycling only. Researchers compared changes in endurance performance, body composition, and muscle performance to determine if there were differences between groups.

Read the detailed description

The purpose of this study was to compare the effects of plyometric- and cycle-oriented high-intensity interval training on body composition, aerobic capacity, and skeletal muscle size, quality, and function in recreationally trained females. Young (21.7 ± 3.1 yrs), recreationally active females were randomly assigned to 8 weeks of twice weekly plyometric (n = 15) or cycling (n = 15) high-intensity interval training. The plyometric-oriented Les Mills BODYATTACK program was used for the plyometric group whereas Les Mills SPRINT, which exclusively involves stationary cycling, represented the cycling group. Both protocols involved alternating high-intensity and recovery intervals, and participants were consistently instructed to give maximal effort during the 'work' periods.

The 30 min plyometric routines included four blocks of high-intensity exercise intervals. The 'work' portions consisted of the following exercises: high-knee runs, plyometric lunges, jumping jacks, squat jumps, burpees, and speed-agility patterns. The recovery periods consisted of complete rest (transitioning between exercises), a light jog, or a low impact stepping motion. On average, participants were instructed to give maximal effort for 1-2 min, with recovery intervals of 15-45 sec. Four separate routines were used throughout the duration of the study, keeping one routine per week; participants completed each routine a total of 4 times within a session.

The 30 min cycling routines were performed on upright stationary bikes (Schwinn, AC Performance, Chicago, IL). Protocols involved 'work' ranging from 20-80 sec with recovery intervals between 10-60 sec. Recovery intervals consisted of complete rest on bike or particularly slow cycling. Resistance and cycling speed were relatively variable across sessions, with some intervals of higher resistance and lower speed and others involving lower resistance and higher speed (e.g., >120 RPMs). The same four workouts were used throughout the duration of the study alternating each week.

Body composition (4-compartment model), VO2peak, countermovement jump performance, muscle size and echo intensity (muscle quality) as well as strength and power of the knee extensors and plantar flexors were measured before and after training. Body composition testing was completing using dual-energy x-ray absorpiometry, air displacement plethysmogrphay, and bioeletrical impedance. VO2peak was measured using a standardized maximal exercise test on a treadmill. Countermovement jump height and power was recorded with participants performing jumps on a force plate. Muscle size and quality were determined using non-invasive ultrasonography. Finally, serum growth hormone responses to the VO2peak test were measured before and after the protocols.

Conditions
Healthy
Being tested
High-Intensity Interval Training

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • High-Intensity Interval TrainingBehavioural

    The training intervention is a popular exercise format that consist of alternating brief bouts of high-intensity efforts with bouts of light effort or complete rest.

Study groups in NCT05821504
Study groupRoleWhat they receive
Plyometric High-Intensity Interval TrainingExperimentalThis group performed high-intensity interval training consisting of body-weight, plyometric exercises involving jumping.
Receives: Behavioral: High-Intensity Interval Training
Cycling High-Intensity Interval TrainingExperimentalThis group performed high-intensity interval training consisting of cycling exercise.
Receives: Behavioral: High-Intensity Interval Training

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Muscle composition at baseline

    echo-intensity value derived from ultrasound that indicates the amount of fat infiltration in muscle

    Measured: Pre-intervention

  2. Muscle composition after 8-week intervention

    echo-intensity value derived from ultrasound that indicates the amount of fat infiltration in muscle

    Measured: At week 9

Secondary outcomes (20)
  1. Fat mass at baseline

    Amount of fat tissue a person possesses

    Measured: Pre-intervention

  2. Fat mass after 8-week intervention

    Amount of fat tissue a person possesses

    Measured: At week 9

  3. Group average growth hormone response (concentration at microLiters/Liters) at baseline

    The acute, exercise-induced response for growth hormone

    Measured: Pre-intervention

  4. Group average growth hormone response (concentration at microLiters/Liters) after 8-week intervention

    The acute, exercise-induced response for growth hormone

    Measured: At week 9

  5. Countermovement jump height at baseline

    Height of jump

    Measured: Pre-intervention

  6. Countermovement jump height after 8-week intervention

    Height of jump

    Measured: At week 9

  7. Time to peak torque at baseline

    How quickly muscle torque is generated

    Measured: Pre-intervention

  8. Time to peak torque after 8-week intervention

    How quickly muscle torque is generated

    Measured: At week 9

  9. Maximal oxygen consumption at baseline

    Standard measure of maximal oxygen consumption or peak aerobic capacity during exercise

    Measured: Pre-intervention

  10. Maximal oxygen consumption after 8-week intervention

    Standard measure of maximal oxygen consumption or peak aerobic capacity during exercise

    Measured: At week 9

  11. Body fat percentage at baseline

    Relative amount of body fat a person possesses

    Measured: Pre-intervention

  12. Body fat percentage after 8-week intervention

    Relative amount of body fat a person possesses

    Measured: At week 9

  13. Fat-free mass at baseline

    Amount of non-fat tissue a person possesses

    Measured: Pre-intervention

  14. Fat-free mass after 8-week intervention

    Amount of non-fat tissue a person possesses

    Measured: At week 9

  15. Peak torque at baseline

    Strength of a muscle

    Measured: Pre-intervention

  16. Peak torque after 8-week intervention

    Strength of a muscle

    Measured: At week 9

  17. Muscle cross-sectional area at baseline

    The size of a muscle

    Measured: Pre-intervention

  18. Muscle cross-sectional area after 8-week intervention

    The size of a muscle

    Measured: At week 9

  19. Muscle power at baseline

    Product of torque and velocity as determined on a dynamometer

    Measured: Pre-intervention

  20. Muscle power after 8-week intervention

    Product of torque and velocity as determined on a dynamometer

    Measured: At week 9

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Apr 2023
  2. Study start1 Aug 2018
  3. Primary completion21 Nov 2018
  4. Study completion21 Nov 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
Two groups performed different types of high-intensity interval training
Masking
None (open label)
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05821504
Sponsor's protocol ID
2022-0465
Status last verified
Jun 2023
First submitted
14 Mar 2023
Last updated
13 Jun 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: There is no plan to share.

Publications

  • Holmes AJ, Stratton MT, Bailly AR, Gottschall JS, Feito Y, Ha PL, Lavigne A, Persaud K, Gagnon HL, Krueger A, Modjeski A, Esmat TA, Harper LN, VanDusseldorp TA, Hester GM. Effects of plyometric- and cycle-based high-intensity interval training on body composition, aerobic capacity, and muscle function in young females: a field-based group fitness assessment. Appl Physiol Nutr Metab. 2023 Dec 1;48(12):932-945. doi: 10.1139/apnm-2022-0465. Epub 2023 Aug 9.

    PubMed 37556856

Questions about this trial

What is this clinical trial studying?

A study testing High-Intensity Interval Training in people with Healthy, run by Kennesaw State University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 13 Jun 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Muscle composition at baseline (time frame: Pre-intervention). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05821504, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Jun 2023.

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High-Intensity Interval Training and Performance | AzTrials