[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"other\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:other":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,44,70,129],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100585594","education--mentorship-of-advanced-practice-providers-to-increase-community-based-research-within-the-ncorp-network-coach-app-trial-100585594",false,"NCT06904391","Education & Mentorship of Advanced Practice Providers to Increase Community-based Research Within the NCORP Network, COACH-APP Trial","Building Capacity Within the NCORP Network Through an Education and Mentorship Intervention for Advanced Practice Providers (COACH-APP)","COACH-APP","Inclusion Criteria:\n\n* APP PRACTICE: Must have one practicing APP who can dedicate approximately 2 hours\u002Fmonth to participate in the intervention and study activities over a 12-month period, supported by their direct supervisor via the APP Support Statement\n* APP PRACTICE: Must attest to research infrastructure that can support APP trial enrollment, as declared on the APP Practice Attestation\n* APP PRACTICE: Must have submitted the APP Practice Attestation within the Study Interest Survey\n* APP PRACTICE: Must have received the required APP practice ID for Oncology Patient Enrollment Network (OPEN) enrollment in the Study Selection Email prior to enrollment\n* APP PRACTICE: Must enroll eligible practice site(s) in OPEN within 14 days of receiving the Study Selection Email.\n* APP: Practicing nurse practitioner (NP) or physician assistant (PA) registered as an active non-physician investigators (NPIVR) within the National Cancer Institute (NCI) Registration and Credential Repository (RCR)\n* APP: Treats oncology patients at practice that is actively recruiting to NCORP and\u002For NCTN trials\n* APP: Not planning to leave their clinical position within the APP practice (defined as one or more NCORP affiliate or sub-affiliate site\\[s\\] where the APP participating in the study sees patients and clinical research activities occur) in the next 12 months at enrollment\n* APP: Willing to participate in a 30-minute recorded phone interview, if selected\n* APP: Completed and submitted the APP Attestation within the Study Interest Survey\n* APP: Completed and submitted an APP Support Statement from their direct supervisor approving participation in this study, within the Study Interest Survey\n* APP: Identify and obtain signed Research Care (RC) Team Acknowledgements from two members (defined below) of their research care team to assist them in this study. The RC team for this study will consist of an oncologist and clinical research professional (i.e., clinical research coordinator, clinical research associate clinical research nurse, etc.) that the APP collaborated with over the past 6 months or could collaborate with in the future to enroll patients on NCORP and\u002For NCTN trials\n* APP: Must have received the required APP practice ID for OPEN enrollment in the Study Selection Email\n* APP: Must enroll consented APPs in OPEN within 14 days of receiving the Study Selection Email\n* MENTOR: Must be a practicing APP chosen by the WF-2403 COACH-APP Study MPIs\n* MENTOR: Must have the following criteria:\n\n  * Clinical practice experience in a practice that enrolls to NCORP and\u002For NCTN trials.\n  * Participation in a leadership role within NCTN or NCORP (i.e., serving on a Research Base committee, working group, taskforce or as a site PI)\n  * Willing to complete COACH-APP mentor training.\n  * Willing to complete a 30-minute recorded phone interview about their experience with the COACH-APP intervention\n* RESEARCH CARE TEAM INTERVIEW: Must be an identified member of the Research Care Team for an APP assigned to the COACH-APP intervention arm. The Research Care Team will be reviewed by the APP in the 12 month survey for any changes\n* RESEARCH CARE TEAM INTERVIEW: Willing to participate in a recorded phone interview (approximately 30 minutes) to assess their perceptions of the COACH-APP intervention, including feasibility, acceptability, and impact\n\nExclusion Criteria:\n\n* APP PRACTICE: APP practice has an APP serving as a COACH-APP intervention mentor\n* APP PRACTICE: Another APP at the same APP practice is already enrolled in this study (i.e., only 1 APP is allowed per APP practice)\n* APP PRACTICE: Affiliate\u002Fsub-affiliate site(s) within this APP practice are already enrolled or are intended to be enrolled in this study under another APP practice\n* APP: Has already completed the SWOG APP workshop\n* APP: Served as a site principal investigator (PI) for an NCORP or NCTN study at any time\n* APP: Participated as a presenter for the SWOG APP workshop\n* APP: Participated on the planning committee for The Advanced Practice Provider Clinical Trials Research Manual\n* APP: Participated on the planning committee for the SWOG APP workshop\n* APP: Past or current member of SWOG APP Task Force Committee\n* APP: Past or current member of Eastern Cooperative Oncology Group- American College of Radiology Imaging Network (ECOG-ACRIN) APP Committee\n* MENTOR: Must not work at NC002-Wake Forest University Health Sciences or its affiliate\u002Fsubaffiliate sites",true,"ALL","18 Years",{"count":21,"type":22},97,"ESTIMATED","INTERVENTIONAL",[25],"NA","This clinical trial evaluates whether a mentorship and education intervention called COACH-APP works to improve advanced practice providers' (APPs) confidence in their ability to participate in clinical research (research self-efficacy). APPs are skilled clinicians who are routinely part of cancer care teams, but who may not routinely be part of the research care team at community oncology sites. The COACH-APP program provides focused education and structured mentorship to assist in meaningful integration to the research care team, which may increase research self-efficacy among APPs and ultimately improve patient care and access to clinical trials.",[28],"Other",[30],"Mentorship, education intervention, COACH-APP","RECRUITING","2026-04-08",{"date":34,"type":35},"2026-04-09","ACTUAL",{"date":37,"type":35},"2025-09-05",{"date":39,"type":22},"2028-06-30",{"name":41,"class":42},"Wake Forest University Health Sciences","OTHER",31,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":4,"targetDuration":4,"studyType":51,"phases":4,"briefSummary":52,"conditions":53,"keywords":61,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":4,"completionDateStruct":4,"leadSponsor":67,"locationsCount":4},"100609534","karyopharm-expanded-access-program-for-selinexor-100609534","NCT07215832","Karyopharm Expanded Access Program for Selinexor","KEAP","Inclusion Criteria:\n\n\\-\n\nExclusion Criteria:\n\n\\-","EXPANDED_ACCESS","KEAP is an expanded access program designed to provide selinexor to eligible participants outside of a clinical trial before the drug has been given marketing approval by the country's regulatory agency or the drug is commercially available in the country. Patients who do not qualify for an ongoing clinical trial but who might benefit from the investigational medicine may be eligible, provided they have exhausted all other available treatment options. Investigational medicines are provided to patients only through treating physicians who obtain the relevant approval on behalf of their patient from the relevant regulatory agency and follow all applicable safety-reporting regulations of the respective country.",[54,55,56,57,58,59,60,28],"Multiple Myeloma","Diffuse Large B-Cell Lymphoma (DLBCL)","Sarcoma","Neuroglioblastoma","Peripheral T-cell Lymphoma","Endometrial Cancer","Myelofibrosis",[62],"selinexor","AVAILABLE","2026-02-26",{"date":66,"type":35},"2026-03-02",{"name":68,"class":69},"Karyopharm Therapeutics Inc","INDUSTRY",{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":74,"acronym":4,"eligibilityCriteria":75,"healthyVolunteers":17,"sex":18,"minAge":76,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":79,"phases":4,"briefSummary":80,"conditions":81,"keywords":96,"overallStatus":119,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":4},"100609070","healthspan-connect-programme-of-research-100609070","NCT07209774","Healthspan Connect Programme of Research","Inclusion Criteria:\n\n* Age 12 years or older at time of enrollment.\n* Resident in the United Kingdom.\n* Able to participate in the study using digital tools (smartphone, tablet, or computer).\n* Able to provide informed consent (digital consent accepted).\n* For participants aged 12-15 years: must have parent\u002Fguardian consent in addition to their own assent.\n\nExclusion Criteria:\n\n* Individuals unable to provide informed consent (or parental consent where applicable).\n* Individuals not resident in the UK.\n* Individuals unable to complete study requirements due to lack of internet access, inability to use digital devices, or severe digital literacy barriers.","12 Years",{"count":78,"type":22},100000,"OBSERVATIONAL","Healthspan Connect is a new research programme designed to understand what helps people stay healthy as they age. The programme will explore how lifestyle, environment, genetics, and social factors influence healthy ageing and overall wellbeing.\n\nThe programme will recruit participants aged 12 years and older across the UK. By including adolescents, the programme aims to understand how early life behaviours and experiences shape long-term health. There is no upper age limit, and people from all backgrounds are encouraged to participate. Special pathways ensure that young participants provide consent in an age-appropriate way.\n\nHealthspan Connect is a digital and home-based study, meaning participants can take part from home using smartphones, computers, and online surveys. Participants may also be asked to collect samples such as blood, saliva, stool, urine, or other biological specimens at home using easy-to-use kits. In some sub-studies, participants may be invited to attend research visits for additional tests, scans, or clinical assessments. Family members and close contacts may also be invited to participate in some studies.\n\nThrough Healthspan Connect, researchers aim to:\n\n* Identify the biological, environmental, and social factors that help people live longer, healthier lives.\n* Understand how different groups, including those historically underrepresented in research, experience ageing.\n* Explore ways to support behaviour changes that improve health over the lifespan.\n* Provide near real-time information to inform health policies and interventions.\n\nParticipants may also be asked for permission to link their information with health records, education records, and environmental data to better understand health outcomes over time.\n\nThis programme will serve as a flexible platform for multiple sub-studies, allowing participants to contribute to a wide range of research questions related to healthy ageing, resilience, and long-term health. All data and biological samples will be stored securely and used to advance scientific knowledge, with participant privacy carefully protected.",[82,83,84,85,86,87,88,89,90,91,92,93,94,95,28],"Cancer","Mental Health","Ageing Well","Resilience","Cognitive Health","Psychological Health","Environmental Health Effects","Cardiovascular Health","Metabolic Health","Neurological Health","Musculoskeletal Health","Respiratory Health","Allergies","Eye Health",[97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118],"Healthy ageing","Healthspan","Longevity","Ageing resilience","Life course determinants","Multiple long-term conditions","Digital health research","Remote monitoring","Mobile health (mHealth)","Wearables","Biobank","Biological specimen collection","Home-based sample collection","Epidemiology","Longitudinal cohort study","Adolescents and ageing","Underrepresented populations in research","Behaviour change","Environmental exposures","Data linkage","Electronic health records (EHR)","United Kingdom","NOT_YET_RECRUITING","2025-09-29",{"date":122,"type":35},"2025-10-07",{"date":124,"type":22},"2026-01-05",{"date":126,"type":22},"2056-01-05",{"name":128,"class":42},"King's College London",{"id":130,"slug":131,"hasResults":11,"nctId":132,"briefTitle":133,"officialTitle":133,"acronym":4,"eligibilityCriteria":134,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":135,"targetDuration":137,"studyType":79,"phases":4,"briefSummary":138,"conditions":139,"keywords":140,"overallStatus":119,"whyStopped":4,"lastUpdateSubmitDate":144,"lastUpdatePostDateStruct":145,"startDateStruct":147,"completionDateStruct":149,"leadSponsor":151,"locationsCount":153},"100568906","reliabltyvalidity-of-the-turkish-version-of-the-knap-100568906","NCT06687317","Reliabılıty,Validity Of The Turkish Version Of The KNAP","Inclusion Criteria: Physiotherapy and rehabilitation department students and physiotherapists who speak Turkish -\n\nExclusion Criteria: Physiotherapy and rehabilitation students and physiotherapists who do not speak Turkish.\n\n\\-",{"count":136,"type":22},300,"1 Month","This study, we performed the Turkish version validity and reliability of the KNAP",[28],[141,142,143],"Validity","Reliability","Version","2024-11-12",{"date":146,"type":35},"2024-11-13",{"date":148,"type":22},"2024-12-01",{"date":150,"type":22},"2025-12-01",{"name":152,"class":42},"Gazi University",2]