Comparison of Maximal Oxygen Uptake Obtained Via Seismofit and Cardiopulmonary Exercise Test

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT07554404

Enrollment

Registered

2026-04-28

Start date

2025-10-09

Completion date

2025-12-05

Last updated

2026-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

VO2 Max

Brief summary

This study aims to validate the Ventriject Seismofit device by comparing VO2 Max obtained via the Seismofit and traditional Cardiopulmonary Exercise Testing.

Interventions

OTHERVO2 Max

Comparing maximal oxygen uptake obtained from Cardiopulmonary Exercise Test and Seismofit

Study design

Observational model

COHORT

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

Yes

Inclusion criteria

* Healthy adults 18-65 years old * Provide health history questionnaire and informed consent

Exclusion criteria

* Known chronic disease (cardiovascular, pulmonary, and/or metabolic disease) * Orthopedic Concern * Acute illness during day of test * Severe Hypertension (SBP \>200 and/or DBP \> 110) at rest * Reported pregnancy

Design outcomes

Primary

Measure	Time frame	Description
VO2 Max	Cross-sectional data collected at one time. Total data collection will occur over 3 months.	Maximal oxygen uptake obtained via Cardiopulmonary Exercise Test on a cycle, as well as the Seismofit at rest.

Secondary

Measure	Time frame	Description
Body Fat %	Cross-sectional data collected at one time. Total data collection will occur over 3 months.	Body Fat % will be obtained via Bod Pod.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 29, 2026