Not yet recruiting NCT06830447
Test-retest Reliability of Myocene
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: low-frequency fatigue.
- Who it may be relevant to
- Registry conditions: Reliability, Fatigue. Basic parameters: 18 years — 40 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Test-retest Reliability of Low-frequency Fatigue Assessed Using Myocene
Overview
The test retest reliability of Myocene will be tested.
Interventions
- Other low-frequency fatigue
Low frequency fatigue tested with myocene
Primary outcome measures
- low-frequency fatigue [Time frame: baseline and 30 minutes post baseline.]
Eligibility criteria
Inclusion criteria
- active individuals
Exclusion criteria
- injured participants
- unhealthy volunteers
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06830447 · Myo_testretest