Bâtiment Synathlon, quartier UNIL-Centre
Lausanne, 1015, Switzerland
Location status: Recruiting
NCT Number: NCT05908214
In the present project, the investigators aim at proposing innovative ways of investigating spinal motoneuron hyperexcitability to counteract the associated impairments by using wide pulse high frequency neuromuscular electrical stimulation (WPHF NMES) in various populations. The investigators will use WPHF NMES contractions as a model to gain insights into the mechanisms underlying muscle cramps, restless legs syndrome or stroke-induced spasticity as there is evidence that they share common underlying mechanisms. The investigators will then use WPHF NMES as a training modality to improve plantar flexor neuromuscular function in stroke patients by taking advantage of their motoneuronal hyperexcitability.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Lausanne, 1015, Switzerland
Location status: Recruiting
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
STROKE PATIENTS:
Contraindications for stroke patients:
PEOPLE PRONE TO MUSCLE CRAMPS:
PATIENTS WITH RESTLESS LEGS SYNDROME:
To be included in the study, RLS patients will have to satisfy the Diagnostic criteria for RLS published by the International Restless Legs Syndrome StudyGroup (IRLSSG). All five key clinical features are required for the diagnosis:
They will also have to satisfy the following criteria:
HEALTHY PARTICIPANTS:
Plantar flexors will be stimulated with wide pulse high frequency neuromuscular electrical stimulation 3 times a week for 6 weeks
Time frame: through study completion, an average of 8 weeks
Change from baseline maximal voluntary contraction force after the six-week training period in stroke patients
Time frame: through study completion, an average of 8 weeks
Change from baseline NMES-evoked force after the six-week training period
Time frame: through study completion, an average of 2 weeks
Comparison of NMES-evoked force in plantar flexor muscles between patients (prone to cramps or restless legs) and healthy volunteers
Time frame: through study completion, an average of 8 weeks
Change from baseline estimates of persistent inward current after the six-week training period in stroke patients
Time frame: through study completion, an average of 8 weeks
comparison of estimates of persistent inward current strength in plantar flexor muscles between patients (prone to cramps or restless legs) and healthy volunteers
Time frame: through study completion, an average of 8 weeks
Change from baseline voluntary activation level and contractile properties of the plantar flexor muscles after the six-week training period in stroke patients
Time frame: through study completion, an average of 2 weeks
comparison of voluntary activation level and contractile properties of the plantar flexor muscles between patients (prone to cramps or restless legs) and healthy volunteers
Time frame: through study completion, an average of 8 weeks
Change from baseline Ashworth scale score (minimal score 0, maximal score 4, a higher score means a worst outcome) after the six-week training period in stroke patients
Time frame: through study completion, an average of 8 weeks
functional test
Time frame: through study completion, an average of 8 weeks
functional test
Time frame: through study completion, an average of 8 weeks
functional test
Time frame: through study completion, an average of 8 weeks
change from baseline soleus Hoffmann reflex amplitude after the six-week training period in stroke patients
Time frame: through study completion, an average of 2 weeks
comparison of soleus Hoffmann reflex amplitude between patients (prone to cramps or restless legs) and healthy volunteers
Time frame: through study completion, an average of 2 weeks
comparison between participants reporting muscle cramps and healthy volunteers
Contact information is provided by the study sponsor or research team.
University of Lausanne
Other
Acronym: MnHyperex
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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