[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"patient-navigation\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:patient-navigation":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,51],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100635138","a-lay-navigation-intervention-for-patients-with-lung-cancer-100635138",false,"NCT07548788","A Lay Navigation Intervention for Patients With Lung Cancer","Feasibility and Acceptability of the Care and Connect Program for Patients With Lung Cancer","Inclusion Criteria:\n\n* Patient with diagnosis of non-small cell lung cancer (NSCLC) or small cell lung cancer (SCLC) of any stage\n* Age ≥ 18\n* Have completed their first medical appointment at the Medical Oncology Lung Cancer Clinic at Princess Margaret Cancer Centre (PM), University Health Network\n* Cognitive capacity to consent and complete questionnaires\n\nExclusion Criteria:\n\n* Behavioural safety alert on medical record that would make their participation in Care \\& Connect inappropriate\n* Enrolment in another navigation study within University Health Network\n* Patients who come to PM for a clinical trial visit\n* Inability to communicate and read in English","ALL","18 Years",{"count":19,"type":20},50,"ESTIMATED","INTERVENTIONAL",[23],"NA","Background: In Canada, lung cancer accounts for approximately 25% of cancer deaths each year. There are also known sociodemographic and racial inequities in the diagnosis and treatment of lung cancer. Studies have consistently found that patients with cancer have a high number of unmet needs, including psychological, physical, and informational. Navigation programs represent a potentially promising, equitable, and cost-effective approach to address the unmet needs of patients with lung cancer, but there is limited evidence about their effectiveness in patients with lung cancer. The investigators developed and have implemented a volunteer lay navigator program, Care and Connect (C\\&C), which aims to proactively reduce distress in patients, provide information and support, and increase access to treatment and supportive care resources. The proposed pilot randomized controlled trial (RCT) project plans to 1) assess the feasibility and acceptability of referral to C\\&C and, 2) examine the preliminary effectiveness of C\\&C.\n\nMethods: The current study is a 2-arm, parallel group, mixed methods, pilot RCT with a 1:1 allocation ratio and 3 timepoints: baseline (T0), 3 months (T1), 6 months (T2). It is designed to test the trial feasibility and acceptability of the C\\&C intervention in patients with lung cancer. In total, 50 participants will be randomized to receive the C\\&C intervention or usual care only (25 per arm). At each timepoint, data will be collected on participants' access to psychosocial (PSO) services, psychological wellbeing, and satisfaction with care through participant medical record and a survey. To gain additional insights regarding the acceptability, feasibility, and impact of C\\&C, a subset of 15 participants from the intervention group will be contacted for qualitative exit interviews.\n\nExpected outcomes: There is limited evidence about the effects of lay navigation programs on access to PSO services among patients with lung cancer. This work addresses this knowledge gap by evaluating the feasibility, acceptability, and preliminary impact of C\\&C on patients with lung cancer. The findings of the proposed work will expand the body of evidence supporting lay navigation to the lung cancer population, contributing to the evidence base for patient-centred care.",[26,27,28],"Lung Cancer Non-Small Cell Cancer (NSCLC)","Lung Cancer Small Cell Lung Cancer (SCLC)","Patient Navigation",[30,31,32,33,34,35,36,37],"Lay navigation","Lung cancer","Access to care","Patient navigation","Feasibility","RCT","Pilot","Acceptability","NOT_YET_RECRUITING","2026-04-21",{"date":41,"type":42},"2026-04-23","ACTUAL",{"date":44,"type":20},"2026-04-01",{"date":46,"type":20},"2027-12-01",{"name":48,"class":49},"University Health Network, Toronto","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":57,"eligibilityCriteria":58,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":17,"enrollmentInfo":59,"targetDuration":4,"studyType":21,"phases":61,"briefSummary":62,"conditions":63,"keywords":64,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":83},"100544799","empowering-families-of-migrant-children-and-youth-with-special-healthcare-needs-100544799","NCT06373588","Empowering Families of Migrant Children and Youth with Special Healthcare Needs","Co-design and Evaluation of a Patient Navigator Intervention for Migrant Children and Youth with Special Healthcare Needs (CYSHCN) Experiencing Care Transitions (MiNav Trial)","MiNav","Inclusion Criteria:\n\n* Primary caregiver of child\u002Fyouth ≤18 years who is first- or second-generation migrant, defined as born outside of Canada or having parents born elsewhere, respectively (migrants include immigrants, resettled refugees, refugee claimants (asylum seekers), temporary workers or international students, and other individuals without formal immigration status (undocumented)).\n* Children or youth with special health care needs, as defined by the CYSHCN Screener, which identifies children who are experiencing one or more functional limitation or service use due to a physical, emotional, behavioural, developmental, or other health condition that has lasted or is expected to last at least 12 months.\n* Experiencing care transitions between at least 2 of the following: primary care, community-based care, secondary specialist care, and\u002For hospital-based (acute) care.\n\nExclusion Criteria:\n\n* Caregiver living in Canada ≥10 years\n* Families who are receiving available peer navigation support at sites will be excluded to limit cross-over of interventions.",{"count":60,"type":20},324,[23],"The goal of this randomized controlled trial is to test if a patient navigator program improves healthcare experiences and outcomes for migrant families caring for a child or youth with special healthcare needs (i.e. chronic health condition).\n\nThe main questions are, for migrant families with a child or youth with special healthcare needs:\n\nDoes a patient navigator reduces barriers to care? Does a patient navigator improve care coordination, caregiver empowerment, caregiver stress and quality of life? What are the healthcare experiences for families with and without the patient navigator intervention?\n\nParticipants will:\n\n* Receive the intervention, i.e., the patient navigator program, or continue with standard of care for 12 months\n* Fill out questionnaires at 3 time points on barriers to care, caregiver stress, care coordination, and their child's health",[28],[65,66,28,67,68,69,70,71,72],"Child Health","Chronic health diseases","Migrant population","Refugee","Immigrant","Asylum seeker","Culturally competent care","Health services research","RECRUITING","2024-09-24",{"date":76,"type":42},"2024-09-26",{"date":78,"type":42},"2024-08-13",{"date":80,"type":20},"2027-08",{"name":82,"class":49},"McGill University Health Centre\u002FResearch Institute of the McGill University Health Centre",3]