About this trial
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.
Eligibility criteria
Qualifiers
Aged between 18 and 65 years
Clinically diagnosed with spinal cord injury
Presence of paraplegia
Injury duration of at least 3 months
Disqualifiers
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
Trial design
Treatments tested in this trial
- No intervention