[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"health-related-social-needs\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:health-related-social-needs":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,53,80],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":32,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100646728","the-social-needs-assistance-for-hospitalized-kids-trial-100646728",false,"NCT07687238","The Social Needs Assistance for Hospitalized Kids Trial","Comparing Two Social Needs Assistance Interventions to Improve Health Among Hospitalized Children","SNAK","INCLUSION CRITERIA:\n\nAim 1 - Caregiver-Child Dyads Sample\n\nCaregiver-child dyads will be eligible to participate in the study if they meet the following criteria assessed during the recruitment and enrollment process:\n\n1. children are hospitalized on the general pediatric\u002Fpediatric hospital medicine (PHM) team\u002Fservice\n2. the child is between the ages of 0-17\n3. the child's caregiver is \\>17 years-old\n4. the caregiver speaks English or Spanish\n5. the family lives in the same county as the hospital or in a neighboring county to the hospital\n6. the child is not in Child Protective Services custody\n7. the family has not previously been enrolled in the study\n8. the caregiver screens positive for \\>=1 of the following social risks: food insecurity, housing instability, housing quality concerns, transportation needs, utilities needs, child care needs, or financial strain\n9. the family is not enrolled in another social needs assistance-related research study (e.g., another social needs navigation study)\n\nAim 2 - Caregiver and Community-based Organization (CBO) Qualitative Interviews Sample Caregivers of children enrolled in Aim 1 will be eligible for study interviews.\n\nCBO staff will be eligible to participate if they are:\n\n1. \\> 17 years old\n2. speak English or Spanish\n3. work at a CBO serving the area in which patients at the study sites live\n\nEXCLUSION CRITERIA:\n\nAim 1 - Caregiver-Child Dyads Sample\n\nParticipants will be excluded from participation if they are:\n\n1. not hospitalized or hospitalized outside of general\u002FPHM SERVICE\n2. children are 18 years of age or older\n3. caregiver\u002Fguardians are under the age of 18 years of age\n4. caregivers are do not speak English or Spanish\n5. the family does not live in the same or neighboring county of the recruitment hospital\n6. the child is under the care of Child Protective Services custody\n7. the family has already been previously enrolled in the study\n8. the caregiver does not screen positive for any of the following social risks: food insecurity, housing instability, housing quality concerns, transportation needs, utilities needs, child care needs, or financial strain\n9. the family is already enrolled in a social needs assistance-related research study (e.g., another social needs navigation study)\n\nAim 2 - Caregiver and CBO qualitative interviews Caregivers of children not enrolled in Aim 1 will not be eligible to participate study interviews.\n\nCBO staff will not be eligible to participate if they are:\n\n1. under 18 years of age\n2. do not speak English or Spanish\n3. do not work at a CBO serving the recruitment site areas","ALL",{"count":19,"type":20},1880,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this clinical trial is to determine the best way to help families access social and economic support services in order to improve children's health for hospitalized children and their families\u002Fcaregivers.\n\nThe main question it aims to answer is, does providing active assistance from navigators to connect families to social\u002Feconomic resources lead to greater improvements in child global health compared to providing passive referrals to resources among hospitalized children?\n\nAll families will receive a tailored information sheet with referrals to community resources to address their social\u002Feconomic needs and an introduction to how to search for resources using an online program. Researchers will compare families who receive these resources with families who also receive support from trained navigators, people with knowledge about local resources trained to connect families with resources. The study will examine whether the addition of navigator support improves families' access to services and children's health outcomes.",[26,27,28,29,30,31],"Social Needs","Health-Related Social Needs","Social Determinants of Health (SDOH)","Social Needs Status","Conditions Influencing Health Status","Navigation",[33,34,35,36,37,38,39],"Comparative Effectiveness Research","Randomized Control Trial","Social Determinants of Health","Child, Hospitalized","Hospital Medicine","Patient Navigation","Pediatrics","NOT_YET_RECRUITING","2026-07-03",{"date":43,"type":44},"2026-07-07","ACTUAL",{"date":46,"type":20},"2026-09",{"date":48,"type":20},"2030-09",{"name":50,"class":51},"University of California, San Francisco","OTHER",6,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":4,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":17,"minAge":60,"maxAge":4,"enrollmentInfo":61,"targetDuration":4,"studyType":63,"phases":4,"briefSummary":64,"conditions":65,"keywords":66,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":79},"100601909","catch-a-vibe---24-00864-100601909","NCT07116629","Catch A Vibe - 24-00864","A Community-Based Intervention To Address Health-Related Social Needs For Patients On LAI-PrEP","Inclusion Criteria:\n\nFor Patient participant group: In order to be eligible for participation in this study, an individual must meet all of the following criteria:\n\n* 18 years of age or older\n* Does not have HIV AND vulnerable for HIV infection per WHO, NHS, and CDC recommendations\n* On or initiating LAI-PrEP as part of standard of care prior to study participation\n* Identify as either a Black\u002FLatine cisgender woman OR Black\u002FLatine MSM OR Transgender or Nonbinary Individual\n* Capacity and willingness to provide consent\n\nFor Medical Staff participant group: In order to be eligible for participation in this study, an individual must meet all of the following criteria:\n\n* 18 years of age or older\n* Works with patients who go to the Bellevue Pride Center\n* Be employed at NYU Langone Health or NYC H+H\u002FBellevue as one of the following occupations\n\n  * Physician\n  * Clinical Pharmacist\n  * Nurse\n  * Medical Phlebotomist\n  * Social Worker\u002FNavigator\n  * Community Health Worker\n  * Medical Leader (i.e., director of services)\n\nFor CBO Partner participant group: In order to be eligible for participation in this study, an individual must meet all of the following criteria:\n\n* 18 years of age or older\n* Works with patients who go to the Bellevue Pride Center\n* Be employed at one of the established CBOs\n* Capacity and willingness to provide consent\n\nFor Patient Who Declines LAI-PrEP participant group: In order to be eligible for participation in this study, an individual must meet all of the following criteria:\n\n* 18 years of age or older\n* Declines LAI-PrEP as part of standard of care\n* Capacity and willingness to provide consent\n\nExclusion Criteria:\n\nFor Patient participant group: An individual who meets any of the following criteria will be excluded from participation in this study:\n\n* Less than 18 years old\n* Known HIV seropositive status or test positive at screening\n* Does not identify as one of the listed priority populations\n* Not fluent in either English or Spanish\n* Not interested in HIV PrEP\n* Not willing to consent for study participation\n* Does not reside within New York State\n* Pregnant or planning to become pregnant at the time of consent.\n* Without capacity to consent to participate in the study\n\nFor Medical Staff participant group: An individual who meets any of the following criteria will be excluded from participation in this study:\n\n* Do not work with patients who go to the Bellevue Pride Center\n* Is not employed at NYU Langone Health or NYC\u002FH+H Bellevue as one of the following occupations\n\n  * Physician\n  * Clinical Pharmacist\n  * Nurse\n  * Medical Phlebotomist\n  * Social Worker\n  * Community Health Worker\n  * Medical Leader (i.e., directors of services)\n\nFor CBO Partner participant group: An individual who meets any of the following criteria will be excluded from participation in this study:\n\n• Does not work with patients who go to the Bellevue Pride Center\n\nFor Patient Who Declines LAI-PrEP participant group: An individual who meets any of the following criteria will be excluded from participation in this study:\n\n* Less than 18 years old\n* Interested in initiating LAI-PrEP as part of standard of care or on LAI-PrEP","18 Years",{"count":62,"type":20},343,"OBSERVATIONAL","This study evaluates a proposed community-based implementation strategy to scale up screening, identification, and intervention on Health-Related Social Needs (HRSN) among persons on Long-Acting Injectable Pre-exposure Prophylaxis (LAI-PrEP). To do so, (1) screening for HRSN will occur at provider visits every 4 months, (2) navigation and establishment of connections with community resources through collaboration with two established community-based organization (CBO) partners, and (3) development of a tracking system integrated into the Electronic Medical Record (EMR) for monitoring and assessment of referral outcomes.",[27],[67,68,27],"LAI-PrEP","Community Partnerships","RECRUITING","2026-06-23",{"date":72,"type":44},"2026-06-26",{"date":74,"type":44},"2025-10-22",{"date":76,"type":20},"2028-05",{"name":78,"class":51},"NYU Langone Health",2,{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":86,"eligibilityCriteria":87,"healthyVolunteers":88,"sex":17,"minAge":60,"maxAge":4,"enrollmentInfo":89,"targetDuration":4,"studyType":21,"phases":91,"briefSummary":92,"conditions":93,"keywords":109,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":115,"lastUpdatePostDateStruct":116,"startDateStruct":118,"completionDateStruct":120,"leadSponsor":122,"locationsCount":4},"100619558","communityrx-dementia--peer-navigation-crxdpeer-100619558","NCT07346183","CommunityRx-Dementia + Peer Navigation (CRxDpeer)","CommunityRx-Dementia + Peer Navigation (CRxDpeer): A Real-World Implementation and Effectiveness Study of an IT-Based Social Care Intervention","CRxDpeer","Inclusion Criteria:\n\n* Self-identifies as a caregiver of a home-dwelling person with Alzheimer's disease or related dementias (ADRD)\n* Resides in the target geographic region of the study\n* Has access to a cell phone and agrees to receive text messages from the study\n* Has an email address that they can receive emails from\n* Individuals under the age of 18 who are emancipated minors in the state of Illinois and a caregiver of a person with dementia\n\nExclusion Criteria:\n\n* Minors who are not emancipated in the state of Illinois.\n* Previously participated in the intervention arm of the CommunityRx-Dementia clinical trial",true,{"count":90,"type":20},330,[23],"The CRxDpeer intervention, delivered by a trained peer navigator, in practice called a \"peer mentor\", includes three evidence-based components: (a) focused education about common social (e.g., food and housing insecurity) and caregiving (e.g., respite and end of life care) needs, (b) activation of personalized community resource information for social and caregiving needs through delivery of a resource list (HealtheRx) at the baseline encounter and coaching on how to communicate with service providers, coordinate services and manage social support (e.g., connect with their peer navigator, reach out to friends or relatives for support, identify support groups, etc.) and (c) ongoing navigation-focused support meant to boost the baseline intervention, including a series of proactive text messages over 12 months. During this time, the subject can respond to and communicate with the peer navigator for ongoing support.",[94,95,96,97,27,98,99,100,101,102,103,104,105,106,107,108],"Alzheimer s Disease","Dementia","Caregiver","Loneliness","Social Care","Healthcare Utilization","End of Life Care","Caregiver Burden","Anxiety","Stress","Depression","Self-Efficacy","Peer Support","Implementation Science","Advance Care Planning",[110,111,112,113,114],"resource navigation","peer navigator","peer mentor","social care","dementia caregiver","2026-04-06",{"date":117,"type":44},"2026-04-07",{"date":119,"type":20},"2026-06-01",{"date":121,"type":20},"2029-02-28",{"name":123,"class":51},"University of Chicago"]