Test-retest Reliability of Myocene

Test-retest Reliability of Low-frequency Fatigue Assessed Using Myocene

Status

Not yet recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06830447

Enrollment

Registered

2025-02-17

Start date

2025-03-31

Completion date

2025-05-31

Last updated

2025-02-17

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

Conditions

Fatigue, Reliability

Brief summary

The test retest reliability of Myocene will be tested.

Interventions

OTHERlow-frequency fatigue

Low frequency fatigue tested with myocene

Study design

Observational model

COHORT

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

ALL

Age

18 Years to 40 Years

Healthy volunteers

Yes

Inclusion criteria

* active individuals

Exclusion criteria

* injured participants * unhealthy volunteers

Design outcomes

Primary

Measure	Time frame	Description
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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026