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Experimental for Healthy Subjects

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

Study 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.Check my eligibility
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.See study design
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

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

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.

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Who is running the clinical trial?

University of South CarolinaLead Sponsor
211 Previous Clinical Trials
120,429 Total Patients Enrolled
MAXIMUSUNKNOWN
1 Previous Clinical Trials
55,095 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is there an inclusion criteria specifying that only those younger than 55 years old are eligible for participation in this study?

"Individuals aged between 18 and 35 are eligible for participation in this study. There are currently 71 studies targeting participants below 18 years old and 395 studies focusing on those above the age of 65."

Answered by AI

What are the specific criteria for eligible participants to be enrolled in this medical study?

"To qualify for participation in this research, individuals must be deemed healthy and fall between the ages of 18 to 35. The study aims to enroll approximately 30 eligible participants."

Answered by AI

What is the upper limit of participants that can enroll in this study?

"Indeed, clinicaltrials.gov confirms that this trial is actively enrolling subjects. The study was initially listed on March 18th, 2024 and last revised on April 3rd, 2024. A total of 30 participants are sought from a single site for inclusion in the trial."

Answered by AI

Are patients currently being actively enrolled in this ongoing medical study?

"As per the details found on clinicaltrials.gov, this research project is presently in need of volunteers. The initial posting date for this trial was 3/18/2024, with the most recent revision made on 4/3/2024."

Answered by AI

What are the primary objectives of this medical study?

"The primary objective of this investigation, to be assessed at both Baseline and Week 8, is the alteration in countermovement jump performance. Secondary endpoints encompass variations in positive mood and emotion as evaluated by the Positive and Negative Affect Schedule with a possible range from 0 to 50 - higher values indicate heightened positivity; alterations in body composition including fat percentage, lean mass, and adipose tissue through air-displacement plethysmography; alongside fluctuations in overall mood disruptions determined via the Profile of Mood States (POMS). The composite mood score includes subtracting favorable aspects like vigor and esteem-related emotions from adverse factors such as"

Answered by AI
~20 spots leftby Sep 2024