I suggest that you apply a correlation between time contraction (Tc) and displacement (Dm). In any way you should find any differences between these parameters. For the training, normally, we observe a Tc decreasing and the Dm increasing, this involve a good response following the muscle training. However, can be possible to find another response for the fatigue condition. In any way, look these papers which I sent to you, inside them you will can find others interesting references about your question.
You will find the answer to your question after the perusal of these 3 articles:
https://www.ncbi.nlm.nih.gov/pubmed/27317976
https://www.ncbi.nlm.nih.gov/pubmed/27093538
Decreased Dm and increased Tc have been explained by a reduced efficiency of the excitation- contraction coupling, impairment in membrane conducting properties, and cellular structures destruction. This means that Dm and Tc are useful markers to measure peripheral fatigue. In summary, an increase in Tc + a decrease in Dm = fatigue.
You can to see this PAPER 2015 Wiewelhove "Markers for Routine Assessment of Fatigue and Recovery in Male and Female Team Sport Athletes during High-Intensity Interval Training
Hola Alicia, gracias por tu comentario. Sí, existen otros parámetros (Td, Tr, Ts) y derivadas de los parámetros (Vc, V90, V90, Vrn) pero la baja fiabilidad y alto grado de error de Tr y Ts, hace que estos parámetros no sean útiles en investigación. Por otro lado, el grupo de Alemania liderado por Ferrauti está utilizando para evaluar la fatiga los parámetros Dm, Tc y la derivada V10 Y V90. Bajo mi punto de vista, ese es el camino a seguir. Un saludo.
Dm -a mesure of muscle thickness will increase afer subjects are submitted to physical inactivity (e.g., bed rest); while a decresease in Dm is expected following athletic training.
In field, i have being noticed that DM can increase after endurance running, cycling. The fatigue can induce muscle damaged that does not allow the muscle to maintain the stiffness to got a good response (Something similar to inactivity process, theres are not enough actin-miosine bridges available to have a good muscle stiffness-contraction