Validation of Ventriject Determined Maximal Oxygen Uptake

University of Copenhagen

Status: Completed

Conditions: Healthy

Treatments: Other: Ventriject validation

Study type: Observational

Funder types: Other

Identifiers

NCT03504306

Ventriject1

Details and patient eligibility

About

This study aims to validate the use of the Ventriject product to estimate VO2 max, through a non-physically active test using ECG, echoseismography and echosonography.

Full description

this study will be composed of the following tests:

• blood sample for measurement of blood values
• blood pressure measurement to rule out risks affiliated with maximal effort testing
• DXA body composition scanning
• Measurement on ECG, echosonography and echoseismography with accelerometer, microphone and ECG wires
• Measurements with phone (iPhone)
• VO2 max assessment by maximal oxygen uptake testing on a training bike, using online oxygenmeasurement equipment
• Hand-grip strength assessment

Enrollment: 100 patients

Sex: All

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• healthy adults between 18 and 45 years of age

Exclusion criteria

• current or previous cardiovascular disease
• chronic use of medicine
• pregnancy
• illnesses which prohibits the testing of maximal oxygen uptake