Test-retest Reliability of Myocene
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-40
SponsorUniversity of Maia
About this trial
The test retest reliability of Myocene will be tested.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
active individuals
Disqualifiers
injured participants
unhealthy volunteers
Trial population
Participants will be sports science students, physically active.
Trial design
Design model
Cohort
Time perspective
Cross-sectional
Treatments tested in this trial
low-frequency fatigue
Other interventionLow frequency fatigue tested with myocene
Treatment groups
50 Participants
are divided into 1 treatment groupGroup A: Single group1 intervention
Trial outcomes
Primary outcomes
1
low-frequency fatigue
Low frequency fatigue will be assessed using myocene. Participants will seat on the device with their leg positioned against the "Myo-sensor". Electrical muscle stimulation will be applied using biphasic square waves with a pulse width of 400 µs, delivered through three electrodes. A pre-programmed Myocene protocol, which has a duration of about 2 minutes will be applied
Time frame
baseline and 30 minutes post baseline.Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: