[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"oncology-patients\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:oncology-patients":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,73],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100577573","focus-on-us-adapting-the-focus-program-for-sexual-and-gender-minority-sgm-cancer-patients-and-caregivers-100577573",false,"NCT06800053","FOCUS ON US: Adapting the FOCUS Program for Sexual and Gender Minority (SGM) Cancer Patients and Caregivers","Inclusion Criteria:\n\nPatients must:\n\n1. have been diagnosed or had a biochemical recurrence or progression of any invasive (e.g., Stage ≥1) cancer within the past 24 months;\n2. have at least one informal (unpaid) caregiver willing to participate in the program;\n3. identify as a sexual and\u002For gender minority (SGM) OR have a caregiver who identifies as SGM (e.g., either the patient or caregiver(s) must be SGM);\n4. be age 18 or older;\n5. be able to complete all written and oral components of the study in English;\n6. provide informed consent;\n7. live in the United States.\n\nCaregivers must:\n\n1. self-report having provided support for a cancer patient as an informal (unpaid) caregiver;\n2. have a cancer patient for whom they provided support willing to participate in the program;\n3. identify as a sexual and\u002For gender minority (SGM) OR have provided support to a patient who identifies as SGM (e.g., either the patient or caregiver(s) must be SGM);\n4. be age 18 or older;\n5. be able to complete all written and oral components of the study in English;\n6. provide informed consent;\n7. live in the United States",true,"ALL","18 Years","100 Years",{"count":20,"type":21},160,"ESTIMATED","INTERVENTIONAL",[24],"NA","Our aim for this study is to assess the feasibility and acceptability and explore potential outcomes of the adapted FOCUS On Us intervention in a two-arm pilot trial. The investigators will randomize 80 sexual and\u002For gender minority (SGM; e.g., lesbian, gay, bisexual, transgender, queer, etc.) cancer patients and their ≥80 informal caregivers (total N≥160) to either FOCUS On Us (adapted from the evidence-based FOCUS program) or a waitlist control.",[27,28,29],"Cancer Support","Oncology Patients","Caregivers",[31,32],"Cancer Patients and Caregivers","LGBTQ+","RECRUITING","2026-06-02",{"date":36,"type":37},"2026-06-04","ACTUAL",{"date":39,"type":37},"2025-09-04",{"date":41,"type":21},"2026-06-30",{"name":43,"class":44},"Charles Kamen","OTHER",2,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":72},"100627069","oncology-legal-navigation-study-100627069","NCT07443839","Oncology Legal Navigation Study","Oncology Legal Navigation- Medical Legal Partnership","Inclusion Criteria:\n\n* receiving or have received services at the Markey Cancer Center, University of Kentucky\n* patient with cancer diagnosis\n* caregiver of patient with cancer diagnosis\n* 18 years or older\n* facing legal barriers to care\n\nExclusion Criteria:\n\n* Unable to provide consent",{"count":54,"type":21},60,[24],"The overall objective of this study is to implement a sustainable oncology legal navigation program that will provide direct legal navigation services to help patients and caregivers overcome legal barriers to care in order to reduce cancer-related financial toxicity (FT) and improve health-related quality of life (QOL) among patients\u002Fcaregivers.",[58,28],"Financial Stress",[60,61,62],"Financial toxicity","Hardship","Cost conversations","2026-03-03",{"date":65,"type":37},"2026-03-05",{"date":67,"type":37},"2025-03-24",{"date":69,"type":21},"2026-12-31",{"name":71,"class":44},"Jean Edward",1,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":22,"phases":81,"briefSummary":82,"conditions":83,"keywords":84,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":96,"locationsCount":72},"100587393","utilization-of-virtual-reality-to-increase-comfort-and-reduce-procedural-distress-during-port-insertion-into-the-body-100587393","NCT06927804","Utilization of Virtual Reality to Increase Comfort and Reduce Procedural Distress During Port Insertion Into the Body","Utilization of Virtual Reality to Support Patient Comfort and Reduce Stress During the Implantation of a Subcutaneous Venous Port Prior to the Initiation of Oncological Treatment","Inclusion Criteria:\n\n* Patients \\> 18 years of age\n* Signed Informed Consent Form\n* Patients Indicated for oncology treatment administration using subcutaneous port\n\nExclusion Criteria:\n\n* Not signing of the Informed Consent Form\n* Patients \\\u003C 18 years of age\n* Patients unsuitable for subcutaneous port implantation",{"count":54,"type":21},[24],"This randomised controlled study evaluates whether virtual reality (VR) can support patient comfort and help reduce anxiety and stress during subcutaneous venous port implantation in adult oncology patients. Patients will be assigned to standard care or standard care with VR intervention.\n\nSubjective and objective measures of stress and discomfort will be collected, including the Visual Analog Scale (VAS) for self-reported procedural discomfort, physiological parameters (blood pressure, heart rate, variability), the STAI-6 questionnaire, and salivary cortisol.\n\nThe study aims to explore the potential of VR as a non-pharmacological, immersive tool to improve procedural experience and reduce psychological distress in patients undergo-ing minor oncological procedures.",[28],[85,86,87,88,89],"Virtual reality","subcutaneous venous port","anxiety","stress","pain","2025-12-12",{"date":92,"type":37},"2025-12-19",{"date":94,"type":37},"2025-07-01",{"date":69,"type":21},{"name":97,"class":44},"University Hospital Ostrava"]