Paralysis Clinical Trial
Official title:
Feasibility Study of the Instrumented Evaluation of Eccentric Strengthening in Paresis Patients
he aim of the "RE PAR EX" research is to evaluate the feasibility of the instrumented examination of the effects of eccentric muscle strengthening in paralytic patients. This project is part of the research axis of the movement analysis laboratory. Following a stroke or spinal cord injury, patients develop a spastic paresis syndrome, which is characterized by the appearance of paresis, musculo-tendinous retractions and muscular hyperactivities. If the traditional treatments proposed (stretching, motor work) show limits, the use of eccentric muscle strengthening in paresis patients has been developing for about ten years, with results superior to the usual treatments. The results of the studies evaluating it are focused on clinical evaluations and do not make it possible to identify the precise origin of the observed responses. A pathophysiological understanding of the therapeutic effects of eccentric strengthening would be possible through instrumented examination of muscle structure and function, combining dynamometry, ultrasound, elastrography and electromyography (EMG). However, the feasibility of this quantified instrumental examination in paretic patients during a strengthening protocol has not been evaluated. The feasibility of a quantified instrumented examination in this setting is the aim of this research, a necessary prerequisite for a larger interventional study to evaluate the biomechanical and neurophysiological effects of eccentric muscle strengthening in paretic patients.
n/a
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03780296 -
Implementing Technology Enhanced Real Time Action Observation Therapy in Persons With Chronic Stroke
|
N/A | |
Completed |
NCT00116337 -
Spinal Cord Stimulation to Restore Cough
|
N/A | |
Recruiting |
NCT04736849 -
Epidural and Dorsal Root Stimulation in Humans With Spinal Cord Injury
|
N/A | |
Completed |
NCT00001520 -
The Early Reversibility of Rocuronium After Different Doses of Neostigmine
|
Phase 4 | |
Recruiting |
NCT01556802 -
Use of Minocicline in Patients With Stroke
|
Phase 1 | |
Completed |
NCT00995215 -
Sub-study to Spinal Cord Stimulation to Restore Cough
|
N/A | |
Recruiting |
NCT06069128 -
Evaluate the Usability of the Neuro-trigger Artificial Eye Blinking Stimulation Device in Patients With Paralysis of the Facial Nerve.
|
N/A | |
Completed |
NCT05139732 -
Exploring Functional Paralysis With Advanced Magnetic Resonance Modalities
|
||
Recruiting |
NCT01474148 -
A Neuroprosthesis for Seated Posture and Balance
|
N/A | |
Not yet recruiting |
NCT06169696 -
EMPOWER Early Feasibility Study: Non-invasive BCI to Control a Wheelchair for People With Paralysis
|
N/A | |
Terminated |
NCT04265560 -
Progressive Resistance Training in Acute Spinal Cord Injury
|
N/A | |
Recruiting |
NCT05898334 -
Impact of Biophoton Generator on Chronic-Stroke Patients' Recovery
|
N/A | |
Completed |
NCT05095454 -
Short-Term Transcutaneous or Epidural Spinal Stimulation for Enabling Motor Function in Humans With SCI
|
N/A | |
Recruiting |
NCT01806233 -
Lu's Acupuncture and Moxibustion Treatment on Stroke
|
N/A | |
Recruiting |
NCT05644522 -
Nomad P-KAFO Study
|
N/A | |
Recruiting |
NCT04520373 -
Autologous Adipose Derived Mesenchymal Stem Cells for Spinal Cord Injury Patients
|
Phase 2 | |
Recruiting |
NCT03567239 -
Impact of Custom Assistive and Adaptive Technology in Rehabilitation
|
N/A | |
Recruiting |
NCT00623389 -
Evaluation of an Advanced Lower Extremity Neuroprostheses
|
N/A | |
Withdrawn |
NCT02899858 -
Restoration of Standing and Walking With ISMS in Humans
|
N/A | |
Recruiting |
NCT03827187 -
Awareness Detection and Communication in Disorders of Consciousness
|
N/A |