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Training Adaptations With and Without Ventilatory Training Device

NCT06356181 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2024-12-02

No results posted yet for this study

Summary

This project aims to assess the effectiveness of using a Respiratory Muscle Training (RMT) device during high-intensity functional training (HIFT) to improve fitness and ventilatory parameters. Primary outcome measures include aerobic, anaerobic, and HIFT measures. Secondary measures include sleep, affect, and mood state questionnaires. Participants will be randomized into one of two groups: with the RMT device and without the RMT device.

Conditions

  • Healthy

Interventions

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.

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.

Sponsors & Collaborators

  • MAXIMUS

    collaborator UNKNOWN

  • University of South Carolina

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-03-18
Primary Completion
2024-10-28
Completion
2024-10-29

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06356181 on ClinicalTrials.gov