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Not yet recruiting NCT07549087

Motor Imagery Reaction Time in Individuals With Paraplegic Spinal Cord Injury

Conditions: Spinal Cord Injuries

Sponsor: Istanbul Physical Medicine Rehabilitation Training and Research Hospital

trial.available_in: БГ
Overview
Individuals aged 18-65 years who have been clinically diagnosed with spinal cord injury and have developed paraplegia will be included in the study. Demographic and clinical data of the participants, including age, sex, height, weight, etiology of injury, level of injury, duration of injury, and comorbidities, will be recorded. In addition, disease-specific characteristics such as ambulation status, wheelchair use, presence of incontinence, and presence and severity of pain will be assessed. For the healthy control group, demographic data including age, sex, height, weight, and comorbidities will be recorded. Motor imagery performance of the participants will be evaluated using a computer-based left/right judgment task. In this context, both upper extremity (hand) and lower extremity (foot) images will be used to record reaction time (motor imagery reaction time) and accuracy rate. All tests will be performed under standardized conditions, in a seated position, and using the same device.
Who can participate
Inclusion Criteria: * Aged between 18 and 65 years * Clinically diagnosed with spinal cord injury * Presence of paraplegia * Injury duration of at least 3 months * Medically stable condition * Ability to understand and follow study instructions * Ability to complete the computer-based left/right judgment task * Willingness to participate and provide written informed consent * For the healthy control group: age- and sex-compatible individuals without a history of neurological or major musculoskeletal disease, willing to participate and provide written informed consent Exclusion Criteria: * Tetraplegia * History of other neurological disorders that may affect motor imagery performance * Severe cognitive impairment or communication problems preventing proper participation * Severe visual impairment uncorrected by glasses or lenses * Upper or lower extremity musculoskeletal disorders, deformities, or recent injuries that may affect task performance * Severe psychiatric disorder * Uncontrolled pain or acute medical condition at the time of assessment * Current participation in another interventional clinical study
Interventions
No intervention
OTHER
Locations 1
Turkey (1)
Istanbul Physical Medicine and Rehabilitation Trainig and Research Hospital
Istanbul , Bahcelievler
Technical details
Status
Not yet recruiting
Study type
OBSERVATIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
65 Years
Healthy volunteers
No
Start date
20.04.2026
Completion date
20.05.2026
Registry ID
NCT07549087
Source
clinicaltrials.gov
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