[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"joint-knee-or-hip-replacement\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:joint-knee-or-hip-replacement":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,50,82],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100659961","virtual-reality-therapy-to-improve-arthroplasty-outcomes-100659961",false,"NCT07872670","Virtual Reality Therapy to Improve Arthroplasty Outcomes","Pilot Randomised Controlled Trial of Virtual Reality Immersive Therapy (VRIT) in Addition to Usual Care Compared to Usual Care in Patients Undergoing Joint Arthroplasty - VROOM Trial","VROOM","Inclusion Criteria:\n\n* NHS Highland patients\n* Able to provide written informed consent (remotely)\n* ASA Grade 1 and 2\n* Listed for elective surgery at NHSH NTC\n* Adults\\>18 years undergoing joint arthroplasty surgery (hip and knee) will be included\n* Fluent in English\n* Able to receive and write emails\n* Willing to comply with study protocols\u002Ftraining\n* Access to Wi-Fi to undertake VRIT and complete questionnaires online\n\nExclusion Criteria:\n\n* Not able to provide written informed consent\n* Considered unsuitable by Clinician (with reason)\n* Vision \u002Fhearing difficulties which preclude interaction with immersive environment\n* Unable or unwilling to comply with study procedures and activities\n* Participation in another interventional trial which undermines the scientific basis of the study\n* Have a history of alcohol or substance abuse or Parkinson's disease or Multiple Sclerosis or Labyrinthitis (Ménière's disease), history of seizures, motion sickness or dementia\n* Non NHS Highland patients\n* Photosensitive epilepsy\n* Patients with surgery scheduled for a Friday","ALL","18 Years",{"count":20,"type":21},40,"ESTIMATED","INTERVENTIONAL",[24],"NA","Virtual reality (VR) has recently emerged as a non-medication-based method to manage anxiety. The patient wears a VR headset and is offered an immersive environment with hypnotic components with sound and imagery in a 3D environment. VR creates an immersive 3D environment and diverts attention away from worrying thoughts (anxiety) and pain and has been found useful to manage minor procedural pain and related anxiety.\n\nThis is a pilot feasibility trial to evaluate the effectiveness of VR in improving patient related outcomes (PROM) after joint replacement surgery.",[27,28,29,30],"Surgical","Anxiety","Pain Management","Joint (Knee or Hip Replacement)",[32,33,28,34,35,36],"Psychology","Surgery","Perioperative","Virtual reality","Joint arthroplasty","RECRUITING","2026-10-08",{"date":40,"type":41},"2026-10-13","ACTUAL",{"date":43,"type":41},"2026-03-05",{"date":45,"type":21},"2026-12-01",{"name":47,"class":48},"NHS Highland Research, Development and Innovation Organisation","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":58,"targetDuration":60,"studyType":61,"phases":4,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":81},"100629316","swiss-revision-cohort-100629316","NCT07473089","Swiss Revision Cohort","Swiss Revision Cohort: a Nationwide, Multi-center, Prospective Periprosthetic Joint Infection Cohort Study","REVCO","Inclusion Criteria:\n\n* ≥18 years of age\n* Revision surgery of any large prosthetic joint (i.e., hip, knee, shoulder, ankle, or elbow) performed for a suspected or confirmed periprosthetic joint infections at any of the participating study centres. This includes patients who were previously treated at another hospital and referred to a participating study centre if data on a transferred patient from the previous institution are available, complete, and archived in the institutional patient information system, and the patient underwent at least one surgery at a participating institution.\n* Obtained written informed consent\n* Periprosthetic joint infections diagnosis likely or confirmed according to European Bone and Joint Infection Society criteria\n\nExclusion Criteria:\n\n* Documented objection to subsequent use of personal health data\n* Patient follow-up outside of Switzerland\n* Diagnosis \"periprosthetic joint infections unlikely\" according to European Bone and Joint Infection Society criteria",{"count":59,"type":21},329,"10 Years","OBSERVATIONAL","This study follows patients with infections after a joint replacement over time. During follow-up, treatment outcomes are carefully measured to determine whether the infection can be cured. In addition, factors that may change infection cure rates are examined, including the patient's overall health, the type of bacteria causing the infection, and the surgical and antibiotic treatments used. The goal is to understand what leads to more frequent cure and to improve future care.",[30,64],"Infection as Complication of Medical Care",[66,67,68,69,70,71],"total joint arthroplasty","periprosthetic joint infection","antimicrobial therapy","infection","functional outcomes","patient-reported outcome measures","2026-03-10",{"date":74,"type":41},"2026-03-16",{"date":76,"type":41},"2022-09-23",{"date":78,"type":21},"2030-01",{"name":80,"class":48},"Insel Gruppe AG, University Hospital Bern",5,{"id":83,"slug":84,"hasResults":11,"nctId":85,"briefTitle":86,"officialTitle":87,"acronym":4,"eligibilityCriteria":88,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":89,"enrollmentInfo":90,"targetDuration":4,"studyType":22,"phases":92,"briefSummary":93,"conditions":94,"keywords":95,"overallStatus":100,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":49},"100622435","the-impact-of-extending-sleep-before-joint-replacement-surgery-on-post-surgical-pain-100622435","NCT07383584","The Impact of Extending Sleep Before Joint-replacement Surgery on Post-surgical Pain","Sleep Banking Pre-Surgery for Improved Chronic Post-Surgical Pain: A Pilot Study","Inclusion Criteria:\n\n* Individuals scheduled for a joint replacement surgery (knee or hip) at Naval Medical Center San Diego\n* Aged 18-74 years\n\nExclusion Criteria:\n\n* Individuals \\\u003C 18 or \\>74 years of age at enrollment\n* Individuals diagnosed with untreated sleep disorders\n* Individuals with scheduled timezone travel or work schedule changes (\\>\u002F= 3 hour time change) in the two weeks before surgery","74 Years",{"count":91,"type":21},22,[24],"This study will evaluate the impact of sleep banking on joint replacement surgery recovery.",[30],[96,97,98,99],"sleep banking","sleep extension","chronic pain","recovery","NOT_YET_RECRUITING","2026-02-11",{"date":103,"type":41},"2026-02-12",{"date":105,"type":21},"2026-02-15",{"date":107,"type":21},"2028-01-01",{"name":109,"class":48},"Defense and Veterans Center for Integrative Pain Management"]