Test-retest Reliability of Myocene
- Conditions
- FatigueReliability
- Registration Number
- NCT06830447
- Lead Sponsor
- University of Maia
- Brief Summary
The test retest reliability of Myocene will be tested.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 50
- active individuals
- injured participants
- unhealthy volunteers
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method low-frequency fatigue baseline and 30 minutes post baseline. 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
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.