[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100620094":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":21,"centralContacts":29,"locations":20,"responsibleParty":35,"collaborators":20,"id":37,"slug":38,"hasResults":39,"nctId":40,"briefTitle":41,"officialTitle":41,"acronym":42,"eligibilityCriteria":43,"healthyVolunteers":39,"sex":44,"minAge":45,"maxAge":20,"enrollmentInfo":46,"targetDuration":20,"studyType":49,"phases":50,"briefSummary":52,"conditions":53,"keywords":56,"overallStatus":67,"whyStopped":20,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":20},{"fullName":5,"class":6},"King's College London","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"OASIS VR + Treatment as Usual (TAU)","EXPERIMENTAL","Single-group, open-label feasibility arm. Participants receive a brief virtual reality (VR) program (OASIS) alongside treatment as usual. The VR program is delivered as five supervised sessions over one week (≈20-30 minutes per session) in inpatient, day service, or outpatient settings.",[13],"Behavioral: OASIS virtual reality (VR) program",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"BEHAVIORAL","OASIS virtual reality (VR) program","Immersive VR sessions including (a) food-related exposure scenes, (b) relaxing music, and (c) motivational prompts and goal-setting. Delivered once daily on weekdays for one week (five sessions; ≈20-30 minutes each), supervised by a clinician or trained researcher. Sessions may be paused or stopped at any time.",[9],null,[22,26],{"name":23,"affiliation":24,"role":25},"Hubertus Himmerich, MD, PhD","South London and Maudsley NHS Foundation Trust; King's College London","PRINCIPAL_INVESTIGATOR",{"name":27,"affiliation":24,"role":28},"Janet Treasure, MD, PhD","STUDY_CHAIR",[30],{"name":31,"role":32,"phone":33,"phoneExt":20,"email":34},"Wafa A Alharbi","CONTACT","+447404450403","wafa.alharbi@kcl.ac.uk",{"type":36,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR","100620094","artificial-intelligence-based-virtual-reality-application-to-provide-data--driven-patient-centred-treatment-for-people-with-eating-disorders-100620094",false,"NCT07353151","Artificial Intelligence-based, Virtual Reality Application to Provide Data- Driven, Patient-centred Treatment for People With Eating Disorders","OASIS","Inclusion Criteria:\n\n* Adults ≥18 years.\n* Anorexia nervosa receiving or awaiting treatment as usual (TAU) within South London and Maudsley NHS Foundation Trust (inpatient, day service, or outpatient).\n* Medically stable and clinically suitable to take part in brief VR sessions alongside TAU (as judged by the treating team).\n* Able to give informed consent.\n\nExclusion Criteria:\n\n* Current or recent (within 12 months) serious self-harm with suicidal intent, or behaviour that posed a risk to life (e.g., overdose, deep cutting, swallowing sharp objects), or self-harm likely to cause lasting impairment.\n* Active suicidality or high risk of suicide.\n* Untreated or unstable epilepsy.\n* Psychotic disorder.\n* Outpatient participants with BMI \\\u003C 10.\n* Current participation in another research study or clinical trial.","ALL","18 Years",{"count":47,"type":48},45,"ESTIMATED","INTERVENTIONAL",[51],"NA","The goal of this clinical trial is to see if a short virtual reality (VR) program can be used safely and comfortably with people receiving care for anorexia nervosa. The study will also check if people are willing to take part and complete the full week of VR sessions.\n\nThe main questions the study will answer are:\n\nCan the investigators recruit and keep participants in the study? Do participants complete most of the VR sessions? Do they find the experience helpful and acceptable? Are there any side effects, like nausea or dizziness?\n\nParticipants will:\n\n* Take part in one VR session each weekday (about 20 to 30 minutes) for one week\n* Continue their usual care during this time\n* Answer questions before and after the VR sessions about their anxiety, mood, motivation, and experience\n* Some participants may join a short interview or focus group to share feedback\n\nThe VR program includes scenes for food-related exposure, calming music, motivational phrases, and goal setting. The app was designed with help from people with lived experience of anorexia and based on psychological therapies used in treatment.\n\nWho can take part:\n\n* Adults aged 18 or older\n* People receiving or waiting for care for anorexia nervosa at South London and Maudsley NHS Foundation Trust (SLaM)\n* People who are medically stable and able to give informed consent\n\nWhy this matters:\n\nThis study will help researchers understand if using VR in eating disorder services is practical, safe, and acceptable. The results will help plan a larger trial in the future to see if this type of VR treatment can support recovery from anorexia nervosa. Taking part is voluntary, and participants can stop at any time.",[54,55],"Anorexia Nervosa","Feeding and Eating Disorders",[57,58,59,60,61,62,63,64,65,66],"Anorexia nervosa (AN)","Virtual reality (VR)","Eating disorders","Food exposure","Feasibility study","Food-related anxiety","Exposure-based intervention","South London and Maudsley (SLaM)","King's College London (KCL)","United Kingdom","NOT_YET_RECRUITING","2026-01-19",{"date":70,"type":71},"2026-01-21","ACTUAL",{"date":73,"type":48},"2026-01",{"date":75,"type":48},"2027-08",{"name":5,"class":6}]