Test-retest Reliability of Myocene | Clinical Trial

Key information

Conditions

Reliability Fatigue Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

active individuals

Exclusion criteria

injured participants
unhealthy volunteers

Treatment and study plan

low-frequency fatigue

Other

Low frequency fatigue tested with myocene

Primary outcomes

low-frequency fatigue

Time frame: 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

Sponsors and collaborators

Lead sponsor

University of Maia

Other

Registry information

Official study title

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

Important dates

Study start: 2025
Primary completion: 2025
Study completion: 2025
First posted: Feb 17, 2025
Registry last updated: Feb 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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