Spinal stenosis
Conditions
Interventions
Cognitive behavioral therapy (CBT) will be conducted once preoperatively and twice during postoperative hospitalization, with each session lasting approximately 40-50 minutes. Participants will comple
Sponsors
University of Toyama
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients who will undergo spinal surgery at Toyama University Hospital. Patients whose pain can be evaluated and whose preoperative Visual Analog Scale (VAS) score is greater than 5. Patients who are judged to be eligible for this study by the principal investigator (or sub-investigator) based on medical history, physical examination, and clinical assessment. Patients who have provided written informed consent and who are judged by the principal investigator (or sub-investigator) to be able to comply with the study requirements, undergo the examinations, tests, and surgery necessary for the conduct of this study, and report symptoms during the study period.
Exclusion criteria
Exclusion criteria: Patients who did not provide informed consent to participate in the study. Patients who have difficulty with verbal communication. Patients with a history of cognitive impairment or dementia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Japanese Orthopaedic Association back pain evaluation questionnaire (JOABPEQ) | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain Catastrophizing Scale (PCS) | — |
Countries
Japan
Contacts
Public ContactYuko Mizukami
University of Toyama Department of Orthopaedic Surgery
Outcome results
None listed