[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"scoliosis-patients\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:scoliosis-patients":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,57],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":35,"overallStatus":44,"whyStopped":4,"lastUpdateSubmitDate":45,"lastUpdatePostDateStruct":46,"startDateStruct":49,"completionDateStruct":51,"leadSponsor":53,"locationsCount":56},"100651966","early-phase-1-evaluation-of-an-online-peri-operative-health-education-platform-for-patients-undergoing-spine-surgery-ready-set-recover-100651966",false,"NCT07766824","Evaluation of an Online Peri-operative Health Education Platform for Patients Undergoing Spine Surgery: Ready Set Recover","Inclusion Criteria:\n\n* Patients deemed candidates for medium-\u002Flong-segment spinal fusion\n* Patients who score a \\> 4 on a 0-10 NRS for the question \"How motivated are you to participate in this research study?\"\n* At least 18 years of age and not older than 80 at the time of study enrollment •Ability to read and understand English\n* Daily access to the internet via cell phone, tablet, or computer\n\nExclusion Criteria:\n\n* Have received epidural steroid injection for low back pain, lumbosacral radiculopathy, or scoliosis in the prior 3 months\n* Have received a surgical intervention for low back pain, lumbosacral radiculopathy, or scoliosis in the previous 6 months\n* Concurrent diagnosis of cancer\n* Cognitive impairment\n* Severe comorbidities (e.g., terminal illness, severe organ failure)\n* Non-elective\u002Femergency surgery in the past","ALL","18 Years","80 Years",{"count":19,"type":20},60,"ESTIMATED","INTERVENTIONAL",[23],"EARLY_PHASE1","Chronic back pain is the world's leading cause of disability, with spine surgery being a common yet costly intervention. However, many patients experience suboptimal recovery, with persistent pain and functional limitations contributing to high healthcare utilization and costs. Traditional surgical pathways often overlook the role of mental well-being and patient engagement in recovery. However, research indicates that interventions promoting self-management and stress reduction can lead to improvements in pain, faster recovery, and reduced hospital readmissions.\n\nEvidence shows that preoperative psychosocial factors, such as anxiety and depression, significantly predict post-surgical outcomes, yet structured perioperative support is lacking. To address this gap, Ready Set Recover (RSR), a mobile health (mHealth) intervention, provides education, behavioral strategies, and psychosocial support to enhance surgical preparedness and optimize post-surgical recovery. By addressing both psychological and behavioral factors, RSR has the potential to fill a critical gap in perioperative care. As a scalable digital platform, RSR offers an accessible, cost-effective solution that can be easily integrated into existing surgical care models, reducing the burden on healthcare providers while empowering patients to take an active role in their healing process.\n\nRSR aims to accomplish this by integrating evidence-based components such as cognitive behavioral therapy, mindfulness, gratitude practices, and guided movement to foster patient empowerment and sustainable health practices in the pre- and post-surgical periods. The platform provides patients with a structured and flexible tool to improve self-efficacy, adherence to post-surgical recommendations, and the overall surgical recovery experience.\n\nThis study aims to evaluate the feasibility and acceptability of RSR through an explanatory mixed-methods pilot randomized controlled trial (RCT) in patients undergoing medium-to-long segment spinal fusion at Oregon Health \\& Science University.\n\nAim 1 assesses feasibility and acceptability by measuring patient engagement, intervention completion rates, and satisfaction.\n\nAim 2 qualitatively evaluate barriers and facilitators to implementation of RSR within the clinic setting via provider, patient, and clinic stakeholder semi-structured interviews.\n\nAim 3 establishes a patient community advisory board (CAB) to guide future research and the development of a Phase II Small Business Technology Transfer (STTR) efficacy trial.\n\nFindings from this study will inform the refinement and scalability of RSR as a low-burden, cost-effective solution to improve surgical outcomes. Insights gained from this research may extend beyond spine surgery, informing the development of digital health interventions for other surgical populations, ultimately advancing patient-centered, technology-driven approaches to perioperative care.",[26,27,28,29,30,31,32,33,34],"Medium-\u002FLong-segment Spinal Fusion Patients","Spine Surgeons","Chronic Low Back Pain","Scoliosis Patients","Lumbar Spondylosis","Lumbar Spondylolisthesis","Cervical Spondylosis and Spondylolisthesis","Post Laminectomy Cervical Syndrome","Cervical Myelopathy",[36,37,38,39,40,41,42,43],"back surgery","medium-\u002Flong-segment spinal fusion","mindfulness","Perioperative Care","Whole Person Care","Chronic low back pain","Feasibility","Qualitative","NOT_YET_RECRUITING","2026-08-10",{"date":47,"type":48},"2026-08-17","ACTUAL",{"date":50,"type":20},"2026-09-30",{"date":52,"type":20},"2027-09-30",{"name":54,"class":55},"National University of Natural Medicine","OTHER",1,{"id":58,"slug":59,"hasResults":11,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":63,"eligibilityCriteria":64,"healthyVolunteers":11,"sex":15,"minAge":65,"maxAge":66,"enrollmentInfo":67,"targetDuration":4,"studyType":21,"phases":69,"briefSummary":71,"conditions":72,"keywords":73,"overallStatus":44,"whyStopped":4,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":56},"100649696","feasibility-acceptability-and-preliminary-effects-of-virtual-reality-for-pain-anxiety-and-recovery-enhancement-of-children-post-scoliosis-surgical-repair-100649696","NCT07737886","Feasibility, Acceptability, and Preliminary Effects of Virtual Reality for Pain, Anxiety and Recovery Enhancement of Children Post-scoliosis Surgical Repair","Feasibility, Acceptability, and Preliminary Effects of Virtual Reality for Pain, Anxiety and Recovery Enhancement of Children Post-Scoliosis Surgical Repair: A Pilot Randomized Controlled Parallel Trial (VR-SPINE)","VR-SPINE","Inclusion Criteria:\n\n* Adolescents aged 10 to 17 years hospitalized for corrective scoliosis surgery\n* Stable medical condition\n* Able to communicate in both French and English.\n\nExclusion Criteria:\n\n* Documented photosensitive epilepsy\n* Severe cognitive deficits, preventing assent\n* Prone to motion sickness.\n\nThe investigators will also recruit a sample of (HCP):\n\nInclusion:\n\n-Closely implicated in the care of participants.","10 Years","17 Years",{"count":68,"type":20},24,[70],"NA","Adolescent idiopathic scoliosis is the most common spinal deformity in adolescents and frequently requires surgical intervention when curvature becomes severe. Although surgical correction improves long-term outcomes, the immediate postoperative period is often characterized by significant pain and anxiety, particularly during early mobilization, which can delay participation in physiotherapy and recovery. Virtual reality (VR) has emerged as a promising non-pharmacological intervention for reducing pain and anxiety in pediatric medical settings through immersive distraction and guided engagement.\n\nThe VR-SPINE study is a mixed-methods pilot randomized controlled trial designed to evaluate the feasibility, acceptability, and preliminary clinical effects of a VR-based intervention during early postoperative mobilization in adolescents undergoing scoliosis surgery. 24 participants aged 10-17 years undergoing corrective scoliosis surgery will be recruited at CHU Sainte-Justine and randomized to either VR plus standard postoperative care or standard care alone. The VR intervention consists of a collaborative therapeutic game played during the first postoperative mobilization to an armchair, designed to promote relaxation, distraction, and engagement with physiotherapy.\n\nPrimary outcomes include the feasibility of recruitment and implementation, as well as acceptability and satisfaction among participants and healthcare professionals. Secondary outcomes include postoperative pain, anxiety, tolerance to mobilization, analgesic use, and adverse effects. Qualitative interviews with a subset of participants and healthcare professionals will further explore perceived barriers, facilitators, and the clinical experience of using VR during early recovery.",[29],[74,75,76,77,78,79],"virtual reality","scoliosis","children","pain","anxiety","mobilization","2026-07-27",{"date":82,"type":48},"2026-07-30",{"date":84,"type":20},"2026-07",{"date":86,"type":20},"2028-06-30",{"name":88,"class":55},"St. Justine's Hospital"]