[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100543969":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":32,"centralContacts":36,"locations":26,"responsibleParty":46,"collaborators":48,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":26,"eligibilityCriteria":60,"healthyVolunteers":61,"sex":62,"minAge":63,"maxAge":26,"enrollmentInfo":64,"targetDuration":26,"studyType":67,"phases":68,"briefSummary":70,"conditions":71,"keywords":75,"overallStatus":78,"whyStopped":26,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":26},{"fullName":5,"class":6},"Universidade da Coruña","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"virtual reality","EXPERIMENTAL","The intervention group will perform immersive virtual reality sessions with interactive activities involving functional movements of the spine and limb region in a virtual environment using Meta Quest 3 goggles.",[13],"Device: Virtual Reality",{"label":15,"type":16,"description":17,"interventionNames":18},"Control","ACTIVE_COMPARATOR","The control group will receive conventional physiotherapy treatment based on therapeutic exercise.",[19],"Behavioral: Therapeutic exercise",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","Virtual Reality","The intervention group will engage in immersive virtual reality sessions with interactive activities involving functional movements of the spine and limbs in a virtual environment using Meta Quest 3 goggles. The intervention will last for 6 weeks, comprising a total of 12 sessions, with a maximum duration of 30 minutes of virtual reality and 15 minutes of rest (45 minutes in total per session).",[9],null,{"type":28,"name":29,"description":30,"armGroupLabels":31,"otherNames":26},"BEHAVIORAL","Therapeutic exercise","The control group will receive conventional therapeutic exercise treatment following the recommendations of the Osteoarthritis Research Society International (OARSI), similar to the exercises performed with VR.",[15],[33],{"name":34,"affiliation":5,"role":35},"Beatriz Rodríguez-Romero, PhD","STUDY_DIRECTOR",[37,42],{"name":34,"role":38,"phone":39,"phoneExt":40,"email":41},"CONTACT","00034 981167000","5841","beatriz.romero@udc.es",{"name":43,"role":38,"phone":39,"phoneExt":44,"email":45},"Silvia Rey Abuín","1153","vit@udc.gal",{"type":47,"investigatorFullName":26,"investigatorTitle":26,"investigatorAffiliation":26,"oldNameTitle":26,"oldOrganization":26},"SPONSOR",[49,52],{"name":50,"class":51},"Centre for Information and Communications Technology Research (CITIC)","UNKNOWN",{"name":53,"class":51},"Faculty of Physiotherapy","100543969","knee-osteoarthritis-motor-control-risk-of-falls-and-virtual-reality-100543969",false,"NCT06362785","Knee Osteoarthritis, Motor Control, Risk of Falls and Virtual Reality","Study on the Relationship Between Knee Osteoarthritis, Motor Control and the Risk of Falls, and the Effectiveness of Virtual Reality in Managing It in Older People","Inclusion Criteria:\n\n* Age over 60 years.\n* Non-institutionalized individuals.\n* Subjects who wish and consent through informed consent to participate in the study.\n* Have the ability to walk independently (with or without assistive devices).\n* Diagnosis of primary knee osteoarthritis according to the clinical and radiological criteria of the American College of Rheumatology.\n* Specifically, for phase 1, subjects without a knee osteoarthritis diagnosis will also be included.\n\nExclusion Criteria:\n\n* History of significant previous traumas or surgeries to the spine, pelvis, or legs in the last 12 months.\n* Self-reported presence of dizziness, seizures, or epilepsy, aiming to prevent potential exacerbation of symptoms with VR.\n* Vestibular disorders (balance).\n* Neurological diseases, cardiovascular, or respiratory disorders affecting activity; as well as inflammatory or autoimmune diseases affecting the lower limb joints, and other forms of secondary osteoarthritis.\n* Diagnosis of a terminal illness or a health condition that prevents attendance.\n* To have a medical contraindication for exercise.\n* Body Mass Index (BMI) ≥ 40",true,"ALL","60 Years",{"count":65,"type":66},110,"ESTIMATED","INTERVENTIONAL",[69],"NA","The goal of this clinical trial is to learn about knee osteoarthritis, functionality, and risk of falls in community-dwelling adults aged 60 years and older. The main questions it aims to answer are:\n\n* What are the characteristics of a community-dwelling population over 60 years and older in terms of knee osteoarthritis, functionality, and risk of falls?\n* Does an intervention with virtual reality lower knee osteoarthritis symptoms, raise functionality and prevent falls in community-dwelling adults aged 60 years and older, compared to a control group receiving conventional physiotherapy treatment based on therapeutic exercise?\n\nParticipants will:\n\n* Answer questionnaires.\n* Perform physical laboratory tests through a camera-based motion capture system.\n* Execute task-based exercises in a virtual environment through virtual reality.\n\nResearchers will compare community-dwelling adults aged 60 years and older who execute task based exercises in a virtual environment through virtual reality and community-dwelling adults aged 60 years and older receiving conventional physiotherapy treatment based on therapeutic exercise to see if virtual reality improves knee osteoarthritis symptoms, functionality, and lowers fall risk.",[72,73,74,23],"Knee Osteoarthritis","Task Performance and Analysis","Accidental Falls",[76,73,74,77,23],"Knee osteoarthritis","Aged","NOT_YET_RECRUITING","2025-03-12",{"date":81,"type":82},"2025-03-17","ACTUAL",{"date":84,"type":66},"2025-05-01",{"date":86,"type":66},"2026-06-01",{"name":5,"class":6}]