[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100627913":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":29,"locations":35,"responsibleParty":53,"collaborators":26,"id":56,"slug":57,"hasResults":58,"nctId":59,"briefTitle":60,"officialTitle":61,"acronym":26,"eligibilityCriteria":62,"healthyVolunteers":58,"sex":63,"minAge":64,"maxAge":65,"enrollmentInfo":66,"targetDuration":26,"studyType":69,"phases":70,"briefSummary":72,"conditions":73,"keywords":77,"overallStatus":82,"whyStopped":26,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":92},{"fullName":5,"class":6},"Osijek University Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Standard Multidisciplinary Treatment + Digital Monitoring","EXPERIMENTAL","The intervention group will receive the same multidisciplinary treatment and assessment schedule. In addition, participants will use a smartwatch to continuously monitor physical activity and heart rate and a mobile application to record daily pain intensity, timing of regular analgesic therapy, and use of rescue medication. Study questionnaires will also be completed through the mobile application. Physicians will have continuous access to patient-reported data during the study period.",[13],"Behavioral: tandard Treatment + Digital Monitoring (Intervention Group)",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard Multidisciplinary Treatment (Control Group)","ACTIVE_COMPARATOR","The control group will receive the usual four-week multidisciplinary intervention and complete validated outcome measures at baseline, week 2, and week 4. These measures will assess pain intensity, pain-related disability, quality of life, sleep quality, anxiety, depression, and treatment satisfaction.",[19],"Behavioral: Standard Multidisciplinary Treatment (Control Group)",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"BEHAVIORAL","tandard Treatment + Digital Monitoring (Intervention Group)","The intervention group will receive the same multidisciplinary treatment and assessment schedule. Participants will use a smartwatch to continuously monitor physical activity and heart rate",[9],null,{"type":22,"name":15,"description":17,"armGroupLabels":28,"otherNames":26},[15],[30],{"name":31,"role":32,"phone":33,"phoneExt":26,"email":34},"Ivan Radoš, assoc.prof","CONTACT","00385917974306","irados11@gmail.com",[36],{"facility":37,"status":26,"city":38,"state":26,"zip":39,"country":40,"countryCode":41,"cosmosGeoPoint":42,"geoPoint":47,"contacts":48},"Clinical Hospital Center Osijek","Osijek","31000","Croatia","HR",{"type":43,"coordinates":44},"Point",[45,46],18.6942,45.55066,{"lat":46,"lon":45},[49,50],{"name":31,"role":32,"phone":33,"phoneExt":26,"email":34},{"name":51,"role":52,"phone":26,"phoneExt":26,"email":26},"Ivan Radoš, assoc.prof.","PRINCIPAL_INVESTIGATOR",{"type":52,"investigatorFullName":54,"investigatorTitle":55,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"Ivan Radoš","Principal Investigator","100627913","real-time-treatment-of-chronic-pain-using-digital-intelligence-100627913",false,"NCT07454811","Real-time Treatment of Chronic Pain Using Digital Intelligence","Effectiveness of Digital Intelligence-Supported Real-Time Management in Adults With Chronic Pain: A Randomised Controlled Trial","Inclusion Criteria:\n\n* Age 18-65 years Chronic low back pain significantly affecting disability and\u002For emotional distress\n\n  * Active use of Croatian language\n  * Signed informed consent\n\nExclusion Criteria:\n\n* Age \\\u003C18 or \\>65\n\n  * Acute pain\n  * Previous participation in multidisciplinary program\n  * Pregnancy or cancer-related pain\n  * Psychotic disorders, moderate-severe cognitive impairment, urgent psychiatric conditions\n  * PTSD symptoms, extreme fatigue, low motivation, low literacy\n  * Allergic reactions to metal or silicone","ALL","18 Years","65 Years",{"count":67,"type":68},80,"ESTIMATED","INTERVENTIONAL",[71],"NA","This randomized controlled study will evaluate the effectiveness of real-time digital intelligence in the treatment of chronic pain. A total of 80 adult patients enrolled in a four-week multidisciplinary chronic pain programme will be randomly assigned to either standard treatment alone or standard treatment supported by a smartwatch and a mobile application for real-time monitoring of pain intensity, analgesic use, physical activity, and heart rate.\n\nBoth groups will complete validated questionnaires assessing pain intensity, disability, quality of life, sleep, anxiety, depression, and treatment satisfaction at baseline, two weeks, and four weeks. The intervention group will additionally record daily pain scores and medication use via a mobile application and wear a smartwatch for continuous activity and heart rate monitoring.\n\nThe study aims to determine whether real-time digital monitoring and physician availability improve clinical outcomes compared with standard multidisciplinary care alone.",[74,75,76],"Chronic Pain","Multidisciplinary Biopsychosocial Program","Quality of Life",[78,79,80,81],"digital intelligence","real-time pain treatment","chronic pain","pain management","NOT_YET_RECRUITING","2026-03-02",{"date":85,"type":86},"2026-03-06","ACTUAL",{"date":88,"type":68},"2026-03-09",{"date":90,"type":68},"2028-03-09",{"name":5,"class":6},1]