[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pain-catastrophizing\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pain-catastrophizing":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,49,76],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100640046","empowered-relief-for-cancer-survivors-with-chronic-pain-100640046",false,"NCT07578376","Empowered Relief® for Cancer Survivors With Chronic Pain","Feasibility and Preliminary Efficacy of Empowered Relief® for Cancer Survivors With Chronic Pain","Inclusion Criteria:\n\nHistory of cancer diagnosis, completion of active cancer treatment, cancer free at the time of enrollment, experience of body pain most or every day, pain duration at least 3 months, and English fluency.\n\nExclusion Criteria:\n\nSignificant psychological and cognitive impairment that limits one's ability to complete study tasks (completion of online survey, attending the zoom-based ER class). Life-threatening acute illness (e.g., infection, heart attack, injury), and no access to a computer, a smartphone or a tablet.","ALL","18 Years","120 Years",{"count":20,"type":21},215,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized controlled study to examine the efficacy of ER class in cancer survivors with chronic pain. Eligible participants will be randomly assigned to a ER class or a waitlist control condition. We will recruit 250 participants with a goal of having 200 completers (20% attrition). Participants in the control condition will be invited to attend ER class after the 3-month observation period.",[27,28],"Chronic Pain Due to Cancer","Pain Catastrophizing",[30,31,32,33,34,35],"Empowered Relief","Chronic Pain","Cancer survivor","Survey Study","Monthly follow-ups","Zoom class","RECRUITING","2026-05-11",{"date":39,"type":40},"2026-05-14","ACTUAL",{"date":42,"type":21},"2026-06",{"date":44,"type":21},"2030-04-30",{"name":46,"class":47},"University of Oklahoma","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":16,"minAge":56,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":65,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":4},"100612366","music-therapy-to-reduce-anxiety-and-pain-in-chronic-pain-patients-during-procedures-100612366","NCT07252648","Music Therapy to Reduce Anxiety and Pain in Chronic Pain Patients During Procedures","Effect of Peri-Operative Music Therapy on Anxiety, Pain Catastrophising, and Pain in Chronic Pain Patients Undergoing Interventional Pain Procedures - A Randomised Controlled Trial","Inclusion Criteria:\n\n* aged ≥21years\n* chronic pain ≥3 months\n* scheduled for interventional pain procedures\n\nExclusion Criteria:\n\n* presence of hearing impairment\n* lack of capacity to consent\n* non-interventional pain procedures, e.g. lignocaine infusion, ketamine infusion\n* pregnant women","21 Years",{"count":58,"type":21},110,[24],"This study aims to find out whether listening to music before, during, and after pain procedures can help reduce anxiety, pain catastrophising, and acute pain in patients with chronic pain. Music therapy may provide a simple, safe, and non-drug way to help patients relax and feel more comfortable.\n\nIn this study, adult patients with chronic pain who are scheduled for interventional pain procedures at Singapore General Hospital will be randomly assigned to one of two groups. One group will listen to self-selected music through headphones and speakers before, during, and after the procedure. The other group will receive standard care without music.\n\nResearchers will measure anxiety, pain catastrophising, and pain levels before and after the procedure using validated questionnaires. The main outcome will be the level of anxiety after the procedure. Other outcomes include pain catastrophising scores, pain scores during local anaesthetic injection, and overall patient satisfaction.\n\nThis study will help determine if music therapy can be routinely used to improve comfort and emotional well-being for patients undergoing interventional pain procedures.",[31,62,63,64,28],"Anxiety","Music Therapy","Pain Perception",[28,63,62,31],"NOT_YET_RECRUITING","2026-04-23",{"date":69,"type":40},"2026-04-29",{"date":71,"type":21},"2026-03-30",{"date":73,"type":21},"2026-12-31",{"name":75,"class":47},"Singapore General Hospital",{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":80,"acronym":81,"eligibilityCriteria":82,"healthyVolunteers":83,"sex":84,"minAge":56,"maxAge":85,"enrollmentInfo":86,"targetDuration":4,"studyType":22,"phases":88,"briefSummary":90,"conditions":91,"keywords":94,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":48},"100508052","phase-4-self-adjusted-nitrous-oxide-a-feasibility-study-in-the-setting-of-vasectomy-100508052","NCT05895383","Self-Adjusted Nitrous Oxide: A Feasibility Study in the Setting of Vasectomy","SANO-VAS","Inclusion Criteria:\n\n1. Scheduled for vasectomy\n2. Aged 21 to 85 years\n3. Suitable for receipt of inhaled nitrous oxide\u002Foxygen\n4. Access to an email and computer\n\nExclusion Criteria:\n\n1. Perioral facial hair impeding good mask seal\n2. Cognitive impairment that impedes ability to complete survey questions\n3. Intent to use benzodiazepines or opioids \"as needed\" for purposes of vasectomy\n4. Has any of the following medical conditions, which contraindicate use of nitrous oxide:\n\n   1. Inner ear, bariatric or eye surgery within the last 2 weeks,\n   2. Current emphysematous blebs,\n   3. Severe B-12 deficiency,\n   4. Bleomycin chemotherapy within the past year,\n   5. Heart attack within the past year,\n   6. Stroke within the past year,\n   7. Class III or higher heart failure.",true,"MALE","85 Years",{"count":87,"type":21},35,[89],"PHASE4","This study is being done to see if nitrous oxide during vasectomy decreases pain and anxiety, and also assess whether patients have better satisfaction when they control their own level of nitrous oxide during the procedure. If we find that patients experience less pain or anxiety with nitrous oxide, it could be suggested that self-adjusted nitrous oxide (SANO) may be a useful tool for improving experience of care during vasectomy.",[92,28,93],"Procedural Pain","Procedural Anxiety",[95,96,97,98],"vasectomy","nitrous oxide","experience of care","ambulatory","2026-02-04",{"date":101,"type":40},"2026-02-06",{"date":103,"type":40},"2023-05-24",{"date":105,"type":21},"2027-01-30",{"name":107,"class":47},"Beth Israel Deaconess Medical Center"]