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Modelling neuromuscular responses to electro-mechanical stimuli

Modelling human neuromuscular responses to electro-mechanical stimuli after neurological injuries - Modelling neuromuscular responses to electro-mechanical stimuli

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON49185
Enrollment
75
Registered
2020-05-20
Start date
2021-07-02
Completion date
Unknown
Last updated
2026-03-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

incomplete spinal cord injury, stroke incomplete spinal cord injury, stroke

Interventions

None listed

Sponsors

University of Twente
Lead Sponsor

Eligibility

Age
16 Years to 99 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria: • age between 16 and 85, • legal capacity to give the consent at his/her own will; for the stroke individuals: • hemiparesis of the lower limb at chronic stage (> 3 months); • impaired plantar flexion during walking • MRC Grade 3 and above for the calf • FAC score of 3 and above • Ability to walk at least 6 minutes at their self-selected walking speed. for the SCI individuals: • chronic stage: time since SCI > 12 months, • clear walking impairment but able to walk independently (without support), i.e. Walking Index for Spinal Cord Injury (WISCI) > 1 and spinal cord independence measure (SCIM) > 30, • Motor incomplete spinal cord injury (ASIA impairment scale: C or D), • Injury situated superior to the T9 vertebra. • Ability to walk at least 6 minutes at their walking speed.

Exclusion criteria

Exclusion criteria: Individuals fulfilling one of the following criteria will be excluded: Motor complete spinal cord injury (ASIA impairment scale: A or B), • neuromuscular disease, • pregnancy, • addictive or previous addictive behaviour defined as the abuse of cannabis, opioids or other drugs, • carrier of infectious diseases, • degenerative mental impairment, e.g. dementia, • inability to cooperate, e.g. due to cognitive deficits (in understanding instructions) or a level of motor impairment that does not permit execution of the intended tasks, • subjects suffering from known cardiac conditions (e.g., pacemakers, arrhythmias, and cardiac conduction disturbances) or peripheral neuropathy. • skin sensitivity or allergies as these are typical contraindications for the application of surface EMG electrodes via adhesive elements and conductive gels. • Participating in an ongoing study

Design outcomes

Primary

MeasureTime frame
The primary outcome of this study are models capable of estimating the following neuro-mechanical parameters: joint kinematics, human-machine interaction forces, amplitude of mechanically-induced reflexes, and motor neuron parameters (e.g. discharge rate, inter-spike intervals and coherence between spike trains).

Secondary

MeasureTime frame
All the subjects will be asked to fill out a questionnaire that assesses physical and physiological factors that may be of relevance for the analysis. These characteristics are the following: • Sex • Age (years) • Weight (kg) • Height (m) • Leg length (m) • Use of sedatives and analgesics • Other neurological disorders than stroke/SCI • Chronic pain • History of depression • History of diagnosed cognitive deficit

Countries

Netherlands

Contacts

Public ContactM. Sartori

University of Twente

m.sartori@utwente.nl+31534891441

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Mar 20, 2026