[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Al-Quds University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":99},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,41,69],{"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":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100633654","the-effect-of-psychosocial-support-on-improving-breast-cancer-patients-response-to-medical-treatment-100633654",false,"NCT07529496","The Effect of Psychosocial Support on Improving Breast Cancer Patients Response to Medical Treatment","A Randomized Controlled Trial Assessing the Effect of Psychosocial Support on Improving Breast Cancer's Patients Response to Medical Treatment","Inclusion Criteria:\n\n* age between 20-40 Being Palestinian female from west bank and Jerusalem\n* Diagnosed with stage I-III breast cancer.\n* Currently receiving active medical treatment.\n* Able to provide consent and participate in the intervention.\n\nExclusion Criteria:\n\n* being male.\n* holding other nationalities than Palestinian or living outside the westbank or Jerusalem.\n* Younger than 20 or older than 40 years old.\n* Uncooperative with interviewer\n* Terminally ill (stage IV).\n* Receiving palliative care only.","FEMALE","20 Years","40 Years",{"count":20,"type":21},160,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to evaluate the effect of psychosocial therapy on improving treatment response among breast cancer patients receiving chemotherapy. Participants will be randomized to receive standard medical treatment alone or combined with structured psychosocial therapy. Outcomes include treatment response, psychological well-being, and quality of life.\n\n1. Do psychosocial interventions affect the response to breast cancer treatment?\n2. How do societal attitudes toward psychological and social care influence the willingness of breast cancer patients in Palestine to seek psychosocial interventions?",[27],"Breast Cancer - Female","NOT_YET_RECRUITING","2026-04-07",{"date":31,"type":32},"2026-04-14","ACTUAL",{"date":34,"type":21},"2026-05-01",{"date":36,"type":21},"2027-01-15",{"name":38,"class":39},"Al-Quds University","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":47,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":22,"phases":52,"briefSummary":53,"conditions":54,"keywords":57,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":40},"100580495","assessing-the-impact-of-additional-serratus-anterior-block-within-24-hour-on-postoperative-pain-after-rhomboid-intercostal-block-in-vats-patients-100580495","NCT06838039","Assessing the Impact of Additional Serratus Anterior Block Within 24-Hour on Postoperative Pain After Rhomboid Intercostal Block in VATS Patients","Inclusion Criteria:\n\n1. Adults aged 18-70 years.\n2. Patients undergoing Video-Assisted Thoracoscopic Surgery (VATS).\n3. Classified as ASA physical status I-III (low to moderate surgical risk).\n4. Ability to provide informed consent and follow study protocols.\n\nExclusion Criteria:\n\n1. Known allergy or hypersensitivity to local anesthetics.\n2. Presence of bleeding disorders or anticoagulant use.\n3. History of chronic opioid use or opioid dependence.\n4. Anatomical abnormalities or conditions preventing the application of regional anesthesia (e.g., chest wall deformities).\n5. Presence of neurological disorders affecting pain perception.\n6. Cognitive impairments, language barriers, or inability to communicate effectively.\n7. Pregnancy or breastfeeding.\n8. Refusal or inability to provide informed consent.","ALL","18 Years","70 Years",{"count":51,"type":21},50,[24],"Title: Assessing the Impact of Additional Serratus Anterior Block on Postoperative Pain After Rhomboid Intercostal Block in VATS Patients\n\nPurpose: This randomized controlled trial aims to evaluate whether the addition of a Serratus Anterior Plane Block (SAPB) to the standard Rhomboid Intercostal Block (RIB) improves postoperative pain management in patients undergoing Video-Assisted Thoracoscopic Surgery (VATS).\n\nStudy Design:\n\n* Type: Randomized Controlled Trial (RCT)\n* Participants: 50 patients aged 18 -70 requiring VATS, randomized into two groups: one receiving RIB alone, and the other receiving RIB + SAPB.\n* Duration: Pain and opioid consumption will be measured within 48 hours post-surgery.\n* Outcome Measures: Pain levels using the Visual Analog Scale (VAS), opioid usage, and patient satisfaction.\n\nSignificance:\n\nThe study addresses the gap in research regarding the combined use of SAPB and RIB in pain control for VATS. It hypothesizes that the combination will lead to better pain relief and reduced opioid dependence compared to RIB alone.",[55,56],"Post Operative Pain","VATS",[58,59],"Postoperative Pain Management","Video-Assisted Thoracoscopic Surgery","RECRUITING","2025-08-22",{"date":63,"type":32},"2025-08-28",{"date":65,"type":32},"2025-04-01",{"date":67,"type":21},"2026-12-01",{"name":38,"class":39},{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":56,"eligibilityCriteria":75,"healthyVolunteers":11,"sex":47,"minAge":48,"maxAge":76,"enrollmentInfo":77,"targetDuration":4,"studyType":22,"phases":79,"briefSummary":80,"conditions":81,"keywords":86,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":98},"100580494","intercostal-nerve-block-for-pain-management-after-uniportal-video-assisted-thoracoscopic-surgeries-100580494","NCT06838026","Intercostal Nerve Block for Pain Management After Uniportal Video-assisted Thoracoscopic Surgeries","Internal, External Intercostal Nerve Block and Intercostal Catheter for Pain Management After Uniportal VATS: A Clinical Trial","Inclusion Criteria:\n\n* All participants between the ages of 18 and 80 year-old who have elective or urgent uniportal VATS will be included in the sample.\n\nExclusion Criteria:\n\n* Children - under the age of 18 or participants above the age of 80.\n* Participants with chest wall infections and those with decorticated lungs will be excluded from the study.\n* Participants with pre-existing chest pain or severe renal or hepatic dysfunction\n* Participants with a history of psychiatric disorder or inability to understand the consent form or how to use a Numerical Rating Scale (NRS) for pain measurement\n* Participants who have allergy to any of the given drugs, second thoracic surgery, participation in other clinical trials, obesity with body mass index\\>35 kg\u002Fm2, intake of antiplatelet or anticoagulant agents, spinal deformity and severe bradycardia will also be excluded.\n* Participants will be withdrawn from the study if the technical failure happened in the block or VATS procedure was converted to open procedure.","80 Years",{"count":78,"type":21},90,[24],"The goal of this clinical trial is to compare the safety and effectiveness of the three intercostal nerve blocks used in pain management in uniportal (one port) thoracoscopic surgeries: internal intercostal nerve blocks (ICNB), external ICNB, and Intercostal catheters.\n\nParticipants will be randomly assigned to three groups:\n\n* First group will undergo internal intercostal nerve block\n* Second group will be given external intercostal nerve block\n* Third group will have an intercostal catheter Researchers will compare the three groups to see their impact on post-operative pain management in uniportal VATS.",[82,83,84,85],"Thoracic","Pain, Postoperative","Analgesia","Satisfaction, Patient",[87,88,59,89,90],"Intercostal nerve block","Intercostal Catheter","Post-operative Pain","Patients' Satisfaction","2025-03-26",{"date":65,"type":32},{"date":94,"type":21},"2025-05-05",{"date":96,"type":21},"2026-12-05",{"name":38,"class":39},2,""]