MedPath

Test-retest Reliability of Myocene

Not yet recruiting
Conditions
Fatigue
Reliability
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
Inclusion Criteria
  • active individuals
Exclusion Criteria
  • injured participants
  • unhealthy volunteers

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
low-frequency fatiguebaseline 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
NameTimeMethod

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