Motor Imagery Reaction Time in Individuals With Paraplegic Spinal Cord Injury

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorIstanbul Physical Medicine Rehabilitation Training and Research Hospital

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

Treatment groups

128 Participants
are divided into 2 treatment groups