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Real World Assessment of Resistance Breathing Device

NCT07187349 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 73

Last updated 2026-04-13

No results posted yet for this study

Summary

The purpose of this study is to examine the usability and effectiveness of a stress management device during an academic exam period and asks the following questions:

* To what extent is a resistance breathing device (AIRpen) utilized by participants during the study period?
* What impact does utilizing a resistance breathing device have on participant's well-being when used during a stressful academic period?
* To what extent is a diaphragmatic breathing device acceptable for use when utilized during a noted stress-inducing period such as academic examinations?

Conditions

  • Stress
  • Breathing Exercise
  • Stress Management

Sponsors & Collaborators

  • Purdue University

    collaborator OTHER

  • National Center for Complementary and Integrative Health (NCCIH)

    collaborator NIH

  • Livotion, LLC

    lead INDUSTRY

Eligibility

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

Timeline & Regulatory

Start
2025-12-01
Primary Completion
2026-01-05
Completion
2026-01-05

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 NCT07187349 on ClinicalTrials.gov