Performance and Safety of the PHENIX LIBERTY, a Medical Device for Electrostimulation and Biofeedback, in the Treatment of Musculoskeletal Disorders

NACompletedINTERVENTIONAL
Enrollment

27

Participants

Timeline

Start Date

August 19, 2024

Primary Completion Date

December 18, 2024

Study Completion Date

December 18, 2024

Conditions
Musculoskeletal Disorder
Interventions
DEVICE

Electrical stimulation and biofeedback with Phenix Liberty medical device

"12 sessions of electrical stimulation and biofeedback performed between 6 and 8 weeks at regular intervals according to a schedule drawn up by the physiotherapist.~The patient will undergo 12 therapeutic functional reeducation sessions, at regular intervals according to a schedule drawn up by the physiotherapist, during which the PHENIX LIBERTY device may be used. The patients will complete questionnaires at the end of the care.~Overall, the functional rehabilitation sessions will include muscle testing, electrostimulation and biofeedback.~The follow up will be conduct as follow :~* 12 sessions between 6 and 8 weeks~* 1 end visit, within the week after the 12th session"

Trial Locations (1)

30000

Human Physio, Nîmes

All Listed Sponsors
collaborator

CEISO

INDUSTRY

collaborator

Human Physio

UNKNOWN

lead

Vivaltis

INDUSTRY

NCT05926739 - Performance and Safety of the PHENIX LIBERTY, a Medical Device for Electrostimulation and Biofeedback, in the Treatment of Musculoskeletal Disorders | Biotech Hunter | Biotech Hunter