Scalable Intervention for Stress Management
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-30
SponsorLivotion, LLC
About this trial
The purpose of this research is to measure the acceptance of a resistance breathing intervention and to assess whether it produces physiological and subjective effects in a laboratory setting.
Eligibility criteria
Qualifiers
Be at least 18 years old
Be currently enrolled in a college or university
Be able to read, speak, and comprehend English
Be able and willing to complete a 60-minute study involving heart rate monitoring, survey completion, training, a stress test, and device utilization
Disqualifiers
None
Trial design
Treatments tested in this trial
- Resistance Breathing Device
- Electronic Resistance Breathing Device
Treatment groups
60 Participants
are divided into 3 treatment groupsSponsors and collaborators
Livotion, LLC
Lead sponsor
Purdue University
Collaborator
National Center for Complementary and Integrative Health (NCCIH)
Collaborator
Source ClinicalTrials.gov