{
    "componentChunkName": "component---src-templates-trial-trial-js",
    "path": "/trials/NCT07549087",
    "result": {"pageContext":{"pagePath":"/trials/NCT07549087","trial":{"nct_id":"NCT07549087","brief_title":"Motor Imagery Reaction Time in Individuals With Paraplegic Spinal Cord Injury","official_title":"Upper and Lower Extremity Motor Imagery Reaction Time in Individuals With Paraplegic Spinal Cord Injury: A Comparative Study With Healthy Controls","about_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.\n\nMotor 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.","age_from":18,"age_to":65,"ais_a":false,"ais_b":false,"ais_c":false,"ais_d":false,"ais_e":false,"time_since_injury_from":3,"time_since_injury_from_unit":"months","time_since_injury_to":null,"time_since_injury_to_unit":null,"healthy_volunteers":null,"inclusion_criteria":null,"study_type":"observational","allocation":null,"brief_description":"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.\n\nMotor 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.","detailed_description":null,"final_testing_performed":"0 days","version_id":3,"emsci_trial":false,"curation_status":"uncurated","overall_recruitment_status":"recruiting-soon","primary_intervention":null,"primary_benefit":{"id":5,"name":"General health","parent_id":null,"icon_name":"general-health"},"sex":"All","injury_level_from":"T2","injury_level_to":"S5","start_date":"2026-04-20","organization":"Istanbul Physical Medicine Rehabilitation Training and Research Hospital","benefits":[{"id":1,"name":"Arm/hand function","parent_id":null,"icon_name":"hand-expand"},{"id":5,"name":"General health","parent_id":null,"icon_name":"general-health"},{"id":6,"name":"Mental health and psychosocial factors","parent_id":null,"icon_name":"mental-health"},{"id":12,"name":"Standing/walking/mobility","parent_id":null,"icon_name":"walking"}],"injuries":[],"interventions":[],"outcome_measures":[{"id":67,"name":"Hospital Anxiety and Depression Scale (HADS)","short_name":"HADS","pivot":{"trial_id":8014,"outcome_measure_id":67}}],"recovery_mechanisms":[],"published_at":"2026-05-05T13:44:21.000000Z","modified_at":"2026-05-05T13:44:21.000000Z"},"layout":"trial"}},
    "staticQueryHashes": ["1748999444"]}