Training Adaptations With and Without Ventilatory Training Device
NCT ID: NCT06356181
Last Updated: 2024-12-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
32 participants
INTERVENTIONAL
2024-03-18
2024-10-29
Brief Summary
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Detailed Description
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* Does the device improve fitness parameters: high-intensity functional training, anaerobic capacity, anaerobic peak and mean power output, maximal oxygen uptake, ventilatory threshold, and blood lactate responses to training?
* Does the device improve spirometry measures?
Researchers will compare 6 weeks of training with the ventilatory training device to those without the training device.
Participants will:
* Take part in a total of 8 weeks of study-related activity.
* Complete six total one- to two-hour pre- and post-testing sessions, which include a maximal oxygen uptake test, high-intensity functional training, body composition, spirometry, anaerobic power and capacity testing.
* Complete six weeks of 45-minute high-intensity functional training, three days per week.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Experimental
Participants in this group will undergo 6 weeks of high-intensity functional training using the respiratory muscle training device.
Respiratory Maximus Training Device
Those in the intervention group will wear the respiratory training device for 3 days per week of high-intensity functional training over 6-weeks.
Control
Participants in this group will undergo 6 weeks of high-intensity functional training without using the respiratory muscle training device.
No Respiratory Training Device
Those in the control group will train for 3 days per week of high-intensity functional training over 6-weeks.
Interventions
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Respiratory Maximus Training Device
Those in the intervention group will wear the respiratory training device for 3 days per week of high-intensity functional training over 6-weeks.
No Respiratory Training Device
Those in the control group will train for 3 days per week of high-intensity functional training over 6-weeks.
Eligibility Criteria
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Inclusion Criteria
* Have not participated in HIFT training in the last 6 months.
* Provided written and dated informed consent to participate in the study.
* In good health as determined by medical history and is cleared for exercise.
* Participant will be asked about dietary supplementation use within the past 6 months.
* If participant began taking a supplement within the past month, subject will be asked to discontinue supplement use followed by a 2-week washout prior to participation.
* In all other cases, we will request that participant maintain supplement use.
Exclusion Criteria
* Any metabolic disorder including known electrolyte abnormalities, diabetes, uncontrolled thyroid disease, adrenal disease or hypogonadism.
* Any inborn error of metabolism.
* History of hepatorenal, musculoskeletal, autoimmune, or neurologic disease.
* Participants with a personal history of heart disease, high blood pressure (systolic \>140 mm Hg \& diastolic \>90 mm Hg),
* Participants who are pregnant, planning to become pregnant, or lactating.
18 Years
35 Years
ALL
Yes
Sponsors
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MAXIMUS
UNKNOWN
University of South Carolina
OTHER
Responsible Party
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Shawn M. Arent
Professor and Chair of Exercise Science Department
Locations
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University of South Carolina Sport Science Lab
Columbia, South Carolina, United States
Countries
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Other Identifiers
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Pro00135143
Identifier Type: -
Identifier Source: org_study_id