[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100612949":3},{"organization":4,"armGroups":7,"interventions":23,"overallOfficials":30,"centralContacts":34,"locations":38,"responsibleParty":40,"collaborators":38,"id":42,"slug":43,"hasResults":44,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":48,"eligibilityCriteria":49,"healthyVolunteers":44,"sex":50,"minAge":51,"maxAge":38,"enrollmentInfo":52,"targetDuration":38,"studyType":55,"phases":56,"briefSummary":58,"conditions":59,"keywords":38,"overallStatus":63,"whyStopped":38,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":38},{"fullName":5,"class":6},"Fondazione Policlinico Universitario Agostino Gemelli IRCCS","OTHER",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Study Group","EXPERIMENTAL","patients who resulted anxious at psychological tests who accepted the intensive psychological support",[13],"Other: HADS (Hospital Anxiety and Depression Scale)",{"label":15,"type":16,"description":17,"interventionNames":18},"Pathological Control Group","ACTIVE_COMPARATOR","patients who resulted anxious at psychological tests who refused the intensive psychological support",[13],{"label":20,"type":16,"description":21,"interventionNames":22},"Healthy Control Group","patients who resulted not anxious at psychological tests",[13],[24],{"type":6,"name":25,"description":26,"armGroupLabels":27,"otherNames":28},"HADS (Hospital Anxiety and Depression Scale)","The psychological treatment, for those patients who accepted the enrollment, consists of a weekly 45-minute psychological session for 4 weeks before the recovery in the thoracic department for lung resection. Measurement of psychological test will be collected at the first visit (T0), the day before surgery (T1) and 30 day after surgery (T3); VAS and ISI measurements were collected at T1, the day after surgery (T2) and 30 day after surgery (T3).",[20,15,9],[29],"psychological evaluation",[31],{"name":32,"affiliation":5,"role":33},"Maria Teresa Congedo","PRINCIPAL_INVESTIGATOR",[35],{"name":32,"role":36,"phone":37,"phoneExt":38,"email":39},"CONTACT","+ 390630156845",null,"mariateresa.congedo@policlinicogemelli.it",{"type":41,"investigatorFullName":38,"investigatorTitle":38,"investigatorAffiliation":38,"oldNameTitle":38,"oldOrganization":38},"SPONSOR","100612949","influence-of-a-psychological-intensive-support-program-for-lung-cancer-patients-on-post-operative-outcomes-100612949",false,"NCT07260227","Influence of a PSychological Intensive Support Program for Lung Cancer Patients ON Post-operative Outcomes.","Influence of a PSychological Intensive Support Program for Lung Cancer Patients ON Post-operative Outcomes: a Prospective Clinical Trial (IPSILON Trial).","IPSILON","Inclusion Criteria:\n\n* age more than 18\n* candidate to thoracic resection for lung cancer with radical intent\n* consent to participate in the research study.\n\nExclusion Criteria:\n\n* synchronous cancer requiring chemo or radiotherapy\n* history of chronic pain, vulnerable patients (e.g., minors and\u002For incapacitated subjects)\n* patients with severe psychiatric conditions (psychosis and\u002For personality disorders).","ALL","18 Years",{"count":53,"type":54},138,"ESTIMATED","INTERVENTIONAL",[57],"NA","Anxiety is common among patients diagnosed with lung cancer, affecting 50-60% of cases, and over 30% report moderate to severe psychological distress. This distress includes symptoms such as depression, anxiety and social withdrawal. The waiting period before lung resection often heightens emotional tension due to fears about reduced respiratory function and postoperative dyspnea. Persistent anxiety may continue during follow-up because of the risk of recurrence and the potential need for adjuvant therapy. Previous studies have shown that high perioperative anxiety is associated with longer hospitalization, increased complications, particularly delirium and cardiac arrhythmias, and poorer adherence to treatment.\n\nThis study aims to assess whether a brief, intensive preoperative psychological intervention reduces anxiety levels in lung cancer patients, measured using the Hospital Anxiety and Depression Scale (HADS). Scores of 0-7 indicate normal levels, ≥ 8 probable anxiety or depression. Additional tools include the Visual Analogue Scale (VAS) for pain (0 = no pain, 10 = worst pain imaginable) and the Insomnia Severity Index (ISI) (0-7 no insomnia, 8-14 subthreshold, 15-21 moderate, 22-28 severe). At hospital discharge, patients were invited to complete a questionnaire about satisfaction. Measurement of psychological test will be collected at the first visit (T0), the day before surgery (T1) and 30 day after surgery (T3); VAS and ISI measurements were collected at T1, the day after surgery (T2) and 30 day after surgery (T3).\n\nPatients are divided into three groups: an intervention group receiving four weekly 45-minute psychological sessions, a pathological control group refusing support, and a healthy control group without anxiety. Primary outcomes are changes in HADS scores between T0 and T1; secondary outcomes include complications, pain, insomnia, length of stay, and patient satisfaction. The study is a twelve-month prospective controlled trial with an estimated 46 patients per group",[60,61,62],"NSCLC","Anxiety Postoperative","Depression","NOT_YET_RECRUITING","2025-11-21",{"date":66,"type":67},"2025-12-03","ACTUAL",{"date":69,"type":54},"2025-12-01",{"date":71,"type":54},"2027-04-30",{"name":5,"class":6}]