[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100618349":3},{"organization":4,"armGroups":7,"interventions":30,"overallOfficials":36,"centralContacts":49,"locations":58,"responsibleParty":77,"collaborators":36,"id":81,"slug":82,"hasResults":83,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":36,"eligibilityCriteria":87,"healthyVolunteers":83,"sex":88,"minAge":89,"maxAge":36,"enrollmentInfo":90,"targetDuration":36,"studyType":93,"phases":94,"briefSummary":96,"conditions":97,"keywords":99,"overallStatus":61,"whyStopped":36,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":110},{"fullName":5,"class":6},"University of Aarhus","OTHER",[8,15,21,26],{"label":9,"type":10,"description":11,"interventionNames":12},"Placebo condition","PLACEBO_COMPARATOR","The patient is incorrectly told that stimulation is on",[13,14],"Device: Stimulation OFF","Device: Told ON",{"label":16,"type":17,"description":18,"interventionNames":19},"Total treatment","ACTIVE_COMPARATOR","The patient is correctly told that stimulation is on",[20,14],"Device: Stimulation ON",{"label":22,"type":6,"description":23,"interventionNames":24},"Stimulation treatment","The patient is incorrectly told that stimulation is off",[20,25],"Device: Told OFF",{"label":27,"type":6,"description":28,"interventionNames":29},"Control condition","The patient is correctly told that stimulation is off",[13,25],[31,37,41,45],{"type":32,"name":33,"description":34,"armGroupLabels":35,"otherNames":36},"DEVICE","Stimulation ON","Stimulator will be turned on",[22,16],null,{"type":32,"name":38,"description":39,"armGroupLabels":40,"otherNames":36},"Stimulation OFF","Stimulation is turned off",[27,9],{"type":32,"name":42,"description":43,"armGroupLabels":44,"otherNames":36},"Told ON","Verbal suggestion that stimulation is on",[9,16],{"type":32,"name":46,"description":47,"armGroupLabels":48,"otherNames":36},"Told OFF","Verbal suggestion that stimulation is off",[27,22],[50,55],{"name":51,"role":52,"phone":53,"phoneExt":36,"email":54},"Christina Emborg, Postdoc","CONTACT","+4520910215","chrisemb@psy.au.dk",{"name":56,"role":52,"phone":36,"phoneExt":36,"email":57},"Lene Vase, Professor","lenevase@psy.au.dk",[59],{"facility":60,"status":61,"city":62,"state":36,"zip":63,"country":64,"countryCode":65,"cosmosGeoPoint":66,"geoPoint":71,"contacts":72},"Aarhus University Hospital","RECRUITING","Aarhus N","8200","Denmark","DK",{"type":67,"coordinates":68},"Point",[69,70],10.17317,56.20367,{"lat":70,"lon":69},[73],{"name":74,"role":52,"phone":75,"phoneExt":36,"email":76},"Kaare Meier","+45 24 99 50 34","kaare.meier@clin.au.dk",{"type":78,"investigatorFullName":79,"investigatorTitle":80,"investigatorAffiliation":5,"oldNameTitle":36,"oldOrganization":36},"PRINCIPAL_INVESTIGATOR","Christina Emborg","Postdoc","100618349","does-spinal-cord-stimulation-have-an-effect-beyond-patients-expectations-an-investigation-of-treatment-and-placebo-effects-100618349",false,"NCT07330466","Does Spinal Cord Stimulation Have an Effect Beyond Patients' Expectations? An Investigation of Treatment and Placebo Effects","Does Spinal Cord Stimulation (SCS) Have an Effect Beyond Patients' Expectations? An Investigation of Treatment and Placebo Effects","Inclusion Criteria:\n\n* Patients (\\>18 years of age) with SCS implanted to treat chronic pain.\n* Patients who consent to participation and can cooperate in the study.\n* Use of continuous paresthesia-free SCS for minimum 6 months prior to participation in the study.\n* Pain score of 7 or less on a 0-10 scale in the most painful area treated with SCS, rated upon inclusion.\n* Patients not receiving other neuromodulation treatment.\n* Patients who have not undergone changes in their (pain relevant) medication during the last 30 days (pro necessitate medication allowed).","ALL","18 Years",{"count":91,"type":92},25,"ESTIMATED","INTERVENTIONAL",[95],"NA","The aim of the study is to evaluate treatment outcomes of Spinal Cord Stimulation. In the study each patient participates in four test sessions of 4-5 hours. Patients arrive for test days with their stimulation on. In each test session, baseline pain is first evaluated. Then, SCS is regulated (on\u002Foff) and patients evaluate their pain intensity immidiately and every 15 minutes during the test sessions. Patients are blinded to the treatment conditions during their participation in the study. At all times, patients can resume their usual treatment.",[98],"Spinal Cord Stimulation",[98,100],"Chronic pain","2026-01-04",{"date":103,"type":104},"2026-01-09","ACTUAL",{"date":106,"type":104},"2024-09-01",{"date":108,"type":92},"2027-07",{"name":5,"class":6},1]