Clinical Trial

Real World Assessment of Resistance Breathing Device

Completed
View on ClinicalTrials.gov →
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?
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-09-18.
Status change: Not Yet Recruiting → Completed 2026-04-08
Trial Details
NCT Number NCT07187349
Lead Sponsor Livotion, LLC
Collaborators: Purdue University, National Center for Complementary and Integrative Health (NCCIH)
Conditions Stress, Breathing Exercise, Stress Management
Enrollment 73 participants
Start Date 2025-12-01
Primary Completion 2026-01-05 (estimated)
Study Completion 2026-01-05 (estimated)
Updated on ClinicalTrials.gov 2026-04-13