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Development of motor training after brain and spinal cord lesions

Development of the upper limb motor training that facilitates compensatory neural pathways after brain and spinal cord lesions: a pilot study - Motor training after brain and spinal cord lesions

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000054741
Enrollment
50
Registered
2024-06-25
Start date
2024-06-13
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Cerebral Infarction Traumatic Spinal Cord Injury Spinal Cord Infarction Cervical Spondylotic Myelopathy

Interventions

Upper limb reaching exercise for 5 days

Sponsors

Kyorin University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Criteria for healthy participants: [1] Person who is between 18 and 85 years old [2] Person without history of upper motor impairments due to neurological or musculoskeletal diseases [3] Person who is right-handed Criteria for patients: [1] Person who is between 18 and 85 years old [2] Person who has been diagnosed as cerebral infarction, traumatic cervical spinal cord injury, spinal cord infarction, or cervical spondylotic myelopathy, and shows upper motor neuron sign(s) [3] Person without progression of symptoms more than 6 months after onset or decompression surgeries [4] Person who is able to reach out and grasp a 5 cm square object 30 cm away from the body

Exclusion criteria

Exclusion criteria: [1] Person who has uncontrolled medical conditions (severe heart failure, respiratory failure, diabetes mellitus, hypertension, interstitial pneumonia, kidney failure, autoimmune disease, neoplastic disease, psychiatric disease, infection, or dementia) [2] Person who needs respiratory management with ventilators [3] Person who has intracranial metallic or magnetic pieces, or pacemakers [4] Person who has implantable medical devices, person with history of seizures or epilepsy, person who takes medications, which could lower threshold for seizures (e.g. TCAs, neuroleptic agents), person who is suffering from drug abuse or withdrawal symptoms, person who is pregnant [5] Person who is considered inappropriate to become a participant by a physician [6] Person who has participated in other clinical studies within 12 weeks and has taken medication in the studies [7] Person who is participating in other clinical studies [8] Person who is a minor [9] Person without sufficient comprehension and judgement due to disease or disability even if the person is a major

Design outcomes

Primary

MeasureTime frame
Amplitudes of motor-evoked potentials at the end of intervention

Secondary

MeasureTime frame
Amplitudes of somatosensory-evoked potentials at the end of intervention Electroencephalogram-electromyogram coherence at the end of intervention Electromyogram-electromyogram coherence at the end of intervention Action Research Arm Test score at the end of intervention The Graded Redefined Assessment of Strength, Sensibility and Prehension score at the end of intervention Upper extremity motor score of the international standards for neurological classification of spinal cord injury at the end of intervention Maximum grip strength at the end of intervention Maximum pinch strength at the end of intervention Kinematics of the upper limb during prehension movements at the end of intervention Fingertip forces during prehension movements at the end of intervention

Countries

Japan

Contacts

Public ContactShinya Suzuki

Kyorin University School of Medicine

shinya-suzuki@ks.kyorin-u.ac.jp0422-47-5511

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026