[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"virtual-reality-therapy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:virtual-reality-therapy":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,52,87,109,156,185],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":30,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":51},"100607443","virtual-reality-enhanced-behavioral-activation-for-older-adults-with-depression-100607443",false,"NCT07188623","Virtual Reality-Enhanced Behavioral Activation for Older Adults With Depression","VR-Enhanced BA for Older Adults With Major Depressive Disorder","Inclusion Criteria:\n\n* Patient must meet DSM V criteria for MDD\n* Patient must be at least 65 years of age\n* Patient must be English speaking\n* Without cognitive impairment\n\nExclusion Criteria:\n\n* Substance Use Disorders in past year\n* Any psychosis or bipolar I disorder\n* Any seizure in the last 6 months or untreated epilepsy\n* Current nonsuicidal self-injury or parasuicidal behavior\n* Current suicidal urges and intent\n* Changing psychotherapy treatment within three months of study entry\n* Changing psychotropic medication(s) within two months of study entry","ALL","65 Years",{"count":19,"type":20},30,"ESTIMATED","INTERVENTIONAL",[23],"NA","The primary aims of this study are to assess the feasibility, acceptability, and tolerability of using an immersive virtual reality (VR) headset to engage in behavioral activation (BA) for older adults diagnosed with major depressive disorder (MDD). The secondary aim of this study is to explore the efficacy of using VR to enhance BA therapy in a clinical MDD older adult population.",[26,27,28,29],"Depression - Major Depressive Disorder","Older Adults (65 Years and Older)","Behavioral Activation Treatment","Virtual Reality Therapy",[31,32,33,34,35,36,37,38],"Depression","Older adult","major depressive disorder","MDD","behavioral activation","VR","virtual reality","older adults","RECRUITING","2026-02-18",{"date":42,"type":43},"2026-02-20","ACTUAL",{"date":45,"type":43},"2025-09-30",{"date":47,"type":20},"2026-08",{"name":49,"class":50},"Stanford University","OTHER",1,{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":4,"eligibilityCriteria":58,"healthyVolunteers":11,"sex":16,"minAge":59,"maxAge":4,"enrollmentInfo":60,"targetDuration":4,"studyType":21,"phases":62,"briefSummary":63,"conditions":64,"keywords":70,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":51},"100602565","immersive-virtual-reality-in-cognitive-rehabilitation-of-patients-with-post-stroke-cognitive-impairment-100602565","NCT07125170","Immersive Virtual Reality in Cognitive Rehabilitation of Patients With Post-Stroke Cognitive Impairment","Immersive Virtual Reality in Cognitive Rehabilitation of Patients With Post-Stroke Cognitive Impairment: A Pilot Study at the Department of Physical Medicine and Rehabilitation, Clinical Hospital of the University of Chile","Inclusion Criteria:\n\n* Patients over 18 years of age\n* Patients with a cerebrovascular accident of any etiology with less than 3 months of progression\n* Patients with mild to moderate cognitive impairment post-stroke (impairment in at least one cognitive domain)\n* MoCA score of less than 24 points\n* Referred for cognitive rehabilitation at the Occupational Therapy Unit of HCUCH\n\nExclusion Criteria:\n\n* Patients with refractive errors that prevent the use of the headset\n* Patients with any type of aphasia that prevents the administration of the MoCA test\n* Patients with severe psychiatric disorders (presence of psychotic symptoms or derealization)\n* Patients with severe motor impairments (lack of trunk control or global strength of both upper limbs \\\u003C M3)","18 Years",{"count":61,"type":20},20,[23],"This pilot study aims to evaluate the feasibility of implementing immersive virtual reality (VR) in cognitive rehabilitation for adults with post-stroke cognitive impairment receiving outpatient therapy. Participants will use a head-mounted display and interactive software to engage in gamified cognitive exercises that simulate memory, attention, and executive function tasks. The intervention consists of 10 sessions, delivered two to three times per week over a period of approximately four weeks. The study will assess multiple feasibility indicators, including the recruitment rate based on eligibility criteria, the safety and tolerability of VR sessions for participants, and the usability and satisfaction reported by occupational therapists administering the intervention. Additionally, exploratory outcomes include changes in global cognition and specific cognitive domains, as well as self-reported quality of life. Adverse effects related to VR use will be tracked. This pilot study will help inform the design and implementation of future, larger-scale clinical trials.",[65,66,67,29,68,69],"Stroke","Post-Stroke Cognitive Impairment (PSCI)","Cognitive Dysfunction","Virtual Reality Cognitive Training","Cognitive Rehabilitation",[37,71,72,73,74,75,76,77],"Cognitive rehabilitation","Immersive Therapy","Meta Quest 3","Kinesix XR","Occupational Therapy","Montreal Cognitive Assessment (MoCA)","Simulator Sickness Questionnaire (SSQ)","2025-08-08",{"date":80,"type":43},"2025-08-15",{"date":82,"type":43},"2025-08-06",{"date":84,"type":20},"2026-05-01",{"name":86,"class":50},"University of Chile",{"id":88,"slug":89,"hasResults":11,"nctId":90,"briefTitle":91,"officialTitle":92,"acronym":4,"eligibilityCriteria":93,"healthyVolunteers":11,"sex":16,"minAge":59,"maxAge":4,"enrollmentInfo":94,"targetDuration":4,"studyType":21,"phases":95,"briefSummary":96,"conditions":97,"keywords":4,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":51},"100592902","assessment-and-treat-neglect-patients-with-a-vr-application-100592902","NCT06999473","Assessment and Treat Neglect Patients With a VR Application","Assess and Treat Visuospatial Neglect in Central Neurological Conditions Via an Innovative Virtual Reality Software","Inclusion Criteria:\n\n1. Age 18 years or older\n2. Able to provide informed consent\n3. have had a hemispheric stroke\n\nExclusion Criteria:\n\n1. Have a severe comorbid psychiatric (E.g. psychotic symptoms) disorder\n2. Have a premorbid neurodegenerative disease (E.g. Alzheimer's dementia, vascular dementia)\n3. Have severe written language comprehension deficits\n4. Have a medical implant, such as a cochlear implant or a pacemaker\n5. Have a severe visual impairment that cannot be corrected by wearing glasses while training\n6. Have a history of epileptic seizures The following exclusion criteria do not apply to the Non-VSN stroke group.\n7. Do not show signs of a spatial asymmetry in performance on a battery of screening tasks\n8. Having visual field deficits or lesions in the occipital lobe",{"count":19,"type":20},[23],"The objective of this project is to investigate the effectiveness of neglect training in our self-developed VR application \"SpatialSense\". The investigators aim to reach the following goals:\n\ni. Compare conventional neglect therapy for neglect training with SpatialSense to evaluate the impacts on neglect recovery to see whether the VR therapy improves the clinical outcomes, such as balance recovery, perception of verticality, quality of life, independence in daily activities, and cognitive impairment, after rehabilitation training.\n\nii. Analyze and compare the search strategies employed by stroke patients with VSN and those without VSN during the execution of the search task with SpatialSense to summarize typical visual scanning strategies for facilitation, rehabilitation training, and improving the transfer effect in daily activities.\n\nThe experimental group will receive both conventional OT and PT treatment, but 3 days a week, half an hour of conventional treatment will be replaced by treatment with SpatialSense software. The control group will receive their regular dose-matched conventional OT and PT sessions without interference. The experimental group will receive SpatialSense training 3 times a week for a consecutive 4 weeks (12 sessions in total of 30 minutes).",[98,65,29],"Neglect, Hemispatial","NOT_YET_RECRUITING","2025-05-22",{"date":102,"type":43},"2025-05-31",{"date":104,"type":20},"2025-06-01",{"date":106,"type":20},"2027-07-01",{"name":108,"class":50},"Universiteit Antwerpen",{"id":110,"slug":111,"hasResults":11,"nctId":112,"briefTitle":113,"officialTitle":114,"acronym":4,"eligibilityCriteria":115,"healthyVolunteers":11,"sex":16,"minAge":116,"maxAge":117,"enrollmentInfo":118,"targetDuration":4,"studyType":21,"phases":120,"briefSummary":121,"conditions":122,"keywords":133,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":147,"lastUpdatePostDateStruct":148,"startDateStruct":150,"completionDateStruct":152,"leadSponsor":154,"locationsCount":51},"100520408","the-effect-of-motor-image-training-on-balance-performance-in-geriatric-individuals-100520408","NCT06056180","The Effect of Motor Image Training on Balance Performance in Geriatric Individuals","Investigation of the Effects of Motor Imagery Training Given With Action Observation on Balance Performance in Geriatric Individuals","Inclusion Criteria:\n\n1. To be between 60-80 years old\n2. Having the ability to speak, read, understand and write Turkish\n3. To have the cognitive skills to understand and apply the trainings to be applied in the study (with ≥ 24 points from the Mini Mental State Test)\n4. Being able to do activities of daily living independently\n5. Being able to walk independently (without using a walking aid and at least 10 meters)\n6. Having a body mass index of \\\u003C35 kg\u002Fm2 (not being severely obese or morbidly obese)\n\nExclusion Criteria:\n\n1. Having visual, hearing and sensory impairment\n2. To have had a trauma, lesion or surgery that may affect balance and musculoskeletal system in the last 6 months\n3. Having a history of 2 ≥ falls in the last 6 months\n4. Having any chronic lower extremity pain\n5. Having an acute or chronic illness that may cause problems with balance and falling\n6. Being diagnosed with sensory, vestibular and cerebellar ataxia\n7. Being on any medication that may cause problems with balance, focus, attention and falling.\n8. Exercising regularly, which may affect performance results\n9. To stop participating in the study for any reason","60 Years","80 Years",{"count":119,"type":20},46,[23],"The goal of this study \\[type of study: clinical trial\\] is to was planned to investigate the effect of motor imagery training given to geriatric individuals with action observation on their balance performance and to compare these two methods.\n\nThe main questions it aims to answer are:\n\n1. Is virtual reality-based balance training given together with action observation and motor imagery for six weeks in geriatric individuals more effective in improving static balance than virtual reality-based balance training given alone?\n2. Is virtual reality-based balance training given together with action observation and motor imagery for six weeks in geriatric individuals more effective in improving dynamic balance than virtual reality-based balance training given alone?\n3. Is virtual reality-based balance training given together with motor imagery for six weeks in geriatric individuals more effective in increasing balance confidence than virtual reality-based balance training given alone?\n\n46 geriatric individuals will be randomized into 2 groups. Along with action observation, motor imagery training and virtual reality-based balance training will be given to the study group. On the other hand, only virtual reality-based balance training will be given to the control group. All assessments will be repeated before and after the trainings. The trainings will be applied 2 days a week for 6 weeks. Each training session; 25 minutes for the control group and 45 minutes for the study group.",[123,124,125,29,126,127,128,129,130,131,132],"Imagery (Psychotherapy)","Postural Control","Postural Balance","Surface Electromyography","Geriatric Assessment","Physical Therapy Techniques","Physical Therapy","Healthy Ageing","Healthy Aging","Falling",[134,135,136,137,138,139,140,141,142,143,144,145,146],"visual motor imagery","kinesthetic motor imagery","postural control","virtual reality therapy","interactive video games","balance platform with pressure sensor","surface electromyography","balance confidence","fall risk","mobility","cognitive processing speed","smartphone gyroscope sensor dataset","action observation","2025-05-05",{"date":149,"type":43},"2025-05-08",{"date":151,"type":43},"2023-11-01",{"date":153,"type":20},"2025-12",{"name":155,"class":50},"Muğla Sıtkı Koçman University",{"id":157,"slug":158,"hasResults":11,"nctId":159,"briefTitle":160,"officialTitle":161,"acronym":4,"eligibilityCriteria":162,"healthyVolunteers":11,"sex":16,"minAge":59,"maxAge":163,"enrollmentInfo":164,"targetDuration":4,"studyType":21,"phases":166,"briefSummary":167,"conditions":168,"keywords":173,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":176,"lastUpdatePostDateStruct":177,"startDateStruct":179,"completionDateStruct":181,"leadSponsor":183,"locationsCount":51},"100577025","the-effect-of-virtual-reality-applications-100577025","NCT06792929","The Effect of Virtual Reality Applications","The Effect of Virtual Reality Applications on Diagnostic Procedures Performed in Patients With Suspicious Thyroid Cancer","Inclusion Criteria:\n\n* Patients with suspected thyroid mass\n* No dizziness problem\n* No vision problems\n\nExclusion Criteria:\n\n* Mental health problems that may prevent wearing virtual reality glasses","75 Years",{"count":165,"type":20},100,[23],"Thyroid nodules are a common health problem in the adult population. The majority of cancers are diagnosed by thyroid fine needle aspiration biopsy. Thyroid nodules generally show clinical findings in 1-5% of cases on physical examination and 20-70% on ultrasound examination. In diagnosis; Ultrasonography, fine needle aspiration biopsy, ultrasonography-guided fine needle aspiration biopsy, scintigraphy, computed tomography and magnetic resonance imaging are widely used. The fact that the thyroid fine needle aspiration biopsy procedure is painful, there is no speaking or coughing during the procedure, and in case of insufficient sample, the procedure must be performed several times. Its repetition causes fear and anxiety in patients. A combination of pharmacological and nonpharmacological methods for pain control likely provides the most effective pain relief for the patient. Distraction is one of the non-pharmacological methods used in pain control. Distraction is one of the most preferred methods to reduce pain in patients during diagnosis and treatment procedures. It is a method that allows patients to control and reduce the symptoms they experience by focusing their attention on a different point.The aim of this study is to examine the effect of using a motivational video with virtual reality glasses to distract attention during the biopsy procedure on pain, stress and fear in individuals with suspected thyroid cancer.",[169,29,170,171,172],"Thyroid Cancer","Ultrasound","Fine Needle Aspiration Biopsy","Thyroid Nodule (Diagnosis)",[169,29,170,174,175],"Thyroid Nodule","Fine needle aspiration biopsy","2025-01-24",{"date":178,"type":43},"2025-01-27",{"date":180,"type":20},"2025-02-25",{"date":182,"type":20},"2025-08-30",{"name":184,"class":50},"Dicle University",{"id":186,"slug":187,"hasResults":11,"nctId":188,"briefTitle":189,"officialTitle":190,"acronym":4,"eligibilityCriteria":191,"healthyVolunteers":11,"sex":16,"minAge":59,"maxAge":192,"enrollmentInfo":193,"targetDuration":4,"studyType":21,"phases":195,"briefSummary":196,"conditions":197,"keywords":200,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":205,"lastUpdatePostDateStruct":206,"startDateStruct":208,"completionDateStruct":210,"leadSponsor":212,"locationsCount":51},"100545720","technological-based-rehabilitation-on-individuals-with-rheumatic-disease-100545720","NCT06385574","Technological Based Rehabilitation on Individuals With Rheumatic Disease","The Effects of Technological Based Rehabilitation on Individuals With Rheumatic Disease With Hand Involvement","Inclusion Criteria:\n\n* Having been diagnosed with a rheumatic disease that meets the latest criteria by a rheumatologist\n* Involvement in hand joints (pain, swelling, tenderness)\n* Being 18 years or older\n* Being on stable drug treatment for the last 6 months\n* Having sufficient cooperation to participate in the study\n* Volunteering to participate in the study\n\nExclusion Criteria:\n\n* Not volunteering to participate in the study\n* Having difficulty in cooperating at work\n* Having an additional orthopedic and\u002For neurological disease that will affect hand functions","64 Years",{"count":194,"type":20},45,[23],"Affects such as pain, swelling, tenderness, deformities, limitations, strength and function losses, skill and coordination deficiencies in the hand joints, which are frequently seen in rheumatism patients with hand involvement, are included in body structure and function disorders within the framework of International Classification of Function System. Leap Motion Controller is used in hand rehabilitation because it is small in size, low-cost, portable, non-contact, easy to use and provides visual and auditory feedback. The aim of our study is to examine the effect of technology-based rehabilitation on joint range of motion, grip strength, functionality and disease activity in adult individuals with rheumatic disease with hand involvement; and also to compare these effects with the effects of the hand rehabilitation program implemented under the guidance of a physiotherapist and the control group that continues its routine life.",[198,199,29],"Rheumatic Diseases","Hand Rheumatism",[201,202,203,204],"rheumatic diseases","hand exercises","leap motion","functionality","2024-06-07",{"date":207,"type":43},"2024-06-10",{"date":209,"type":43},"2024-03-15",{"date":211,"type":20},"2024-06-20",{"name":213,"class":50},"Akdeniz University"]