A Validation Study of Force Sense Measurement

CompletedOBSERVATIONAL
Enrollment

30

Participants

Timeline

Start Date

October 1, 2018

Primary Completion Date

March 15, 2019

Study Completion Date

December 15, 2019

Conditions
Knee InjuriesProprioceptive Disorders
Interventions
OTHER

Test protocol for proprioceptive force sense in case group

"* The FS in the knee region was measured by the pressure, biofeedback device (Stabilizer ™, Chattanooga Group Inc., Chattanooga, TN).~* Surface EMG device (Noraxon USA, Inc., Scottsdale, AZ) was used to measure activation levels of M. Vastus Medialis Obliquus (VMO), M. Vastus Lateralis (VL) and M. Rectus Femoris (RF) muscles. Due to the characteristics of the Bipolar Ag/AgCl surface electrodes, the distance between the electrodes was set to 1 cm and the electrode width to 2 cm. The electrode placement was determined according to the SENIAM (Surface ElectroMyoGraphy for the Non-Invasive Assessment of Muscles) criteria."

Trial Locations (1)

06030

Ceyhun Türkmen, Ankara

All Listed Sponsors
lead

Hacettepe University

OTHER

NCT03852199 - A Validation Study of Force Sense Measurement | Biotech Hunter | Biotech Hunter