[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"lumbar-disease\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:lumbar-disease":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":27,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100610744","the-effect-of-mobilization-training-given-to-patients-undergoing-lumbar-stabilization-surgery-on-postoperative-pain-anxiety-kinesiophobia-fear-of-falling-and-mobility-100610744",false,"NCT07231562","The Effect of Mobilization Training Given to Patients Undergoing Lumbar Stabilization Surgery on Postoperative Pain, Anxiety, Kinesiophobia, Fear of Falling, and Mobility","İnclusion Criteria\n\n* The patient must be over 18 years of age\n* Participate in the study voluntarily,\n* Be undergoing lumbar surgery for the first time\n* Be undergoing lumbar stabilization surgery\n* Be oriented to person, place, and time\n* Not have taken any oral or parenteral analgesic medication other than the routine treatment ordered before mobilization\n* Have no restrictions (physical disability, etc.) that would prevent mobilization,\n* Be able to understand and speak Turkish\n* Have no vision or hearing problems,\n* Have no psychiatric illness, ağrı var\n* Be in ASA 1 or 2,\n* Patients planned to be included in the intervention and control groups must not be in the same rooms.\n\nExclusion Criteria\n\n* Having a neurological (such as dementia\u002FAlzheimer's) or psychiatric (such as schizophrenia) medical diagnosis that affects cognitive status.\n* Having a chronic pain disorder.","ALL","18 Years",{"count":18,"type":19},60,"ESTIMATED","INTERVENTIONAL",[22],"NA","In this study, the researcher will examine the effects of preoperative mobilization training (video viewing with VR glasses and brochure methods) given to patients undergoing surgery in the lumbar region on pain, anxiety, fear of movement, fear of falling, and mobility levels in the postoperative period, using specific scales.",[25,26],"Lumbar Disease","Lumbar Surgery",[28,29,30,31,32],"Lumbar region","kinesiophobia","mobilization","nursing care and education","perioperative period","NOT_YET_RECRUITING","2025-11-14",{"date":36,"type":37},"2025-11-17","ACTUAL",{"date":39,"type":19},"2025-11",{"date":41,"type":19},"2026-07",{"name":43,"class":44},"Suleyman Demirel University","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":15,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":45},"100587793","long-term-clinical-follow-up-analysis-of-patients-with-lumbar-disease-100587793","NCT06933004","Long-term Clinical Follow-up Analysis of Patients With Lumbar Disease.","Inclusion Criteria:\n\n1. Aged between 20 and 80 years.\n2. Patients with lumbar spine disorders requiring surgical treatment.\n3. Able to understand the study content after explanation, capable of expressing their experiences, and willing to sign the written informed consent form.\n\nExclusion Criteria:\n\n1. Individuals with impaired decision-making capacity or from vulnerable populations.\n2. Individuals who are unable or unwilling to return for follow-up assessments.","20 Years","80 Years",{"count":55,"type":19},120,"OBSERVATIONAL","This study is a long-term follow-up of postoperative clinical outcomes in patients with lumbar spine disorders, monitoring spine implants SmartMIS Spinal Fixation System and ASA Spinal Fixation System.\n\nPatients will be selected based on inclusion and exclusion criteria. The informed consent process will be initiated by the physician. A questionnaire-based survey will be conducted, which includes the Visual Analog Scale (VAS), Oswestry Disability Index (ODI), and Fusion Rate. Subjects will complete the same questionnaire assessments preoperatively and at 6 ± 3 months, 12 ± 3 months, and 24 ± 3 months postoperatively.\n\nThe total number of subjects to be enrolled is 120. The total duration of the study is expected to be 4 years.",[25],"RECRUITING","2025-04-10",{"date":62,"type":37},"2025-04-17",{"date":64,"type":19},"2025-05",{"date":66,"type":19},"2028-03-31",{"name":68,"class":44},"National Taiwan University Hospital"]