Scalable Intervention for Stress Management
Livotion, LLC · with Purdue University, National Center for Complementary and Integrative Health (NCCIH) · NCT07127575
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–30 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 60
- US sites recruiting
- 1
- Study start
- August 1, 2025
- Record last updated
- August 17, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: Resistance Breathing Device; Electronic Resistance Breathing Device
Conditions: Stress; Diaphragmatic Breathing
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- 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
Exclusion Criteria
-Individuals diagnosed with anxiety or stress and require professional support to cope with these clinical levels of stress or anxiety should not enroll in the study in place of professional assistance.
Recruiting US locations
Purdue University
West Lafayette, IN 47907
Site contact: Milton Aguirre, PhD · 7654960782 · meaguirr@purdue.edu
Study contacts (from the official record)
- Milton E Aguirre, PhD · 7654960782 · meaguirr@purdue.edu
- Amanda Case, PhD · amanda-case@uiowa.edu
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