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Respiratory Training Device for Fitness Improvement

N/A
Recruiting
Research Sponsored by University of South Carolina
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up weeks 3, 5, and 7
Awards & highlights
No Placebo-Only Group

Summary

This trial will test whether using a Respiratory Muscle Training device during high-intensity functional training can improve fitness and breathing parameters. They will measure aerobic, anaerobic, and HIFT performance as primary

Who is the study for?
This trial is for healthy individuals interested in testing how a Respiratory Muscle Training (RMT) device might affect their fitness during high-intensity workouts. Participants should be willing to undergo fitness tests and answer questionnaires about sleep, mood, and feelings.
What is being tested?
The study is comparing the effects of using an RMT device versus not using one during intense exercise routines. It's designed to see if the device can improve aerobic capacity, anaerobic power, and overall performance in high-intensity functional training.
What are the potential side effects?
Since this trial involves healthy subjects and non-invasive interventions, significant side effects are not anticipated. However, participants may experience fatigue or muscle soreness due to the intensity of the workouts.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~weeks 3, 5, and 7
This trial's timeline: 3 weeks for screening, Varies for treatment, and weeks 3, 5, and 7 for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Changes in aerobic capacity
Changes in anaerobic capacity
Changes in countermovement jump
+5 more
Secondary study objectives
Change in blood lactate responses
Changes in body composition
Changes in negative mood and emotion
+3 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: ExperimentalExperimental Treatment1 Intervention
Participants in this group will undergo 6 weeks of high-intensity functional training using the respiratory muscle training device.
Group II: ControlActive Control1 Intervention
Participants in this group will undergo 6 weeks of high-intensity functional training without using the respiratory muscle training device.

Find a Location

Who is running the clinical trial?

University of South CarolinaLead Sponsor
222 Previous Clinical Trials
120,373 Total Patients Enrolled
MAXIMUSUNKNOWN
1 Previous Clinical Trials
55,095 Total Patients Enrolled
~19 spots leftby Nov 2025
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