[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"children-adult\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:children-adult":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,45,72,100],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100487586","teams-r34-1-after-action-reviews-in-child-welfare-services-100487586",false,"NCT05629013","TEAMS R34 #1 After-Action Reviews in Child Welfare Services","R34-1","Inclusion Criteria:\n\nInclusion Criteria for CWS leaders and\u002For caseworkers\n\n1. (For leaders) Employed as one of several CWS leadership positions: CWS Director, CWS Deputy Director, CWS Regional Manager; (For caseworkers) Employed as a caseworker in one of the two participating regions for the proposed study.\n2. Plans to remain employed for at least six months beyond study initiation\n3. Speaks English or Spanish\n\nInclusion Criteria for formal and informal CFT members\n\n1. Member of CFT with one of the participating CWS caseworkers. CFT members can include mental health services provider, Court Appointed Special Advocate (CASA), educational representative, and other supports\n2. Speaks English or Spanish\n\nInclusion Criteria for parents\u002Fcaregivers with active CWS cases\n\n1. Parent\u002Fcaregiver of child aged 6-17 with an open CWS case\n2. Initial CFT meeting for open CWS case has not yet been held (Aim 3)\n3. Speaks English or Spanish\n\nInclusion Criteria for children with active CWS cases (for mental health service linkage data extraction only\\*)\n\n1. Child aged 6-17 with an open CWS case\n2. Mental health services need\u002Fs (identified by the CWS caseworker via CANS screening in advance of the initial CFT meeting, during which consensus is reached regarding the Action Plan and service referral)\n\nExclusion Criteria:\n\nIndividuals who do not meet inclusion criteria are not eligible to participate in this study.","ALL","6 Years",{"count":19,"type":20},320,"ESTIMATED","INTERVENTIONAL",[23],"NA","This project proposes to improve successful mental health service linkage in Child Welfare Services (CWS) by adapting and testing the After Action Review (AAR) team effectiveness intervention to augment the Child Family Team (CFT) services intervention. Despite being both required and a collaborative approach to service planning, CFT meetings are implemented with questionable fidelity and consistency, rarely including children and families as intended. By inclusion of child and family voice, the AAR-enhanced CFT should lead to increased fidelity to the CFT intervention and greater levels of parental satisfaction with the service and shared decision-making, thus resulting in enhanced follow-through with Action Plans and linkage to mental health care for children.",[26,27],"Mental Health Issue","Children, Adult",[29,30,31],"Child Welfare Services","Team Effectiveness Research","Shared Decision Making","RECRUITING","2026-02-02",{"date":35,"type":36},"2026-02-05","ACTUAL",{"date":38,"type":36},"2023-07-28",{"date":40,"type":20},"2027-05-31",{"name":42,"class":43},"University of California, San Diego","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":51,"sex":16,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":21,"phases":56,"briefSummary":57,"conditions":58,"keywords":59,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":44},"100612045","effects-of-battle-rope-training-on-rom-and-pain-in-children-with-post-traumatic-elbow-contractures-100612045","NCT07248475","Effects of Battle Rope Training on ROM and Pain in Children With Post Traumatic Elbow Contractures.","Inclusion Criteria:\n\n* Age 8 to 15\n* Children Suffering from Post-Traumatic Elbow Contracture\n* Written informed consent obtained from the parents or guardians\n* Participants must report a pain level of at least 3 on a visual analog scale (VAS)\n* Children must be able to follow instructions and participate in physical activities.\n* Children without any other co-existing illness like Burn Contractures\n* Either gender will be included\n\nExclusion Criteria:\n\n* Post Traumatic Contracture other than Elbow region\n* Known allergies to materials used in battle rope training.\n* Children who are unable to commit to the training schedule or follow-up assessments.\n* Use of medications that may affect pain perception or muscle function, such as opioids or muscle relaxants.\n* Burn Contracture.\n* Presence of other significant musculoskeletal disorders or neurological conditions affecting the elbow.",true,"8 Years","15 Years",{"count":55,"type":20},42,[23],"The primary objective of this study is to assess the effectiveness of battle rope training in improving ROM, reducing pain, and enhancing overall elbow function in children with post-traumatic elbow contracture. By comparing standard therapy alone to standard therapy plus battle rope training, the study aims to determine if this added intervention leads to greater improvements in functional mobility and pain relief.In this randomized controlled trial, participants will be divided into two groups: a control group, receiving standard treatment (ROM exercises, stretching, and heat therapy), and an intervention group, receiving the same standard treatment plus battle rope training. ROM exercises and stretching will focus on gentle elbow flexion and extension to enhance flexibility, while heat therapy will prepare muscles for movement.\n\nThe intervention group will additionally perform 10-15 minutes of battle rope training, involving dynamic movements that engage the upper body and increase joint activation. Pre- and post-intervention assessments using a goniometer for ROM, the Flynn scoring system for functional and cosmetic outcomes, and the Visual Analogue Scale (VAS) for pain will provide comprehensive data on the effectiveness of the intervention",[27],[60,61,62],"Battle Rope Training","Elbow Contractures","ROM","2025-11-18",{"date":65,"type":36},"2025-11-25",{"date":67,"type":36},"2025-10-29",{"date":69,"type":20},"2026-01-30",{"name":71,"class":43},"Riphah International University",{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":4,"eligibilityCriteria":78,"healthyVolunteers":11,"sex":79,"minAge":52,"maxAge":53,"enrollmentInfo":80,"targetDuration":4,"studyType":21,"phases":82,"briefSummary":83,"conditions":84,"keywords":85,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":44},"100611709","agility-and-sprint-performance-in-youth-soccer-a-comparison-of-fifa-11-and-ramp-protocols-100611709","NCT07244107","Agility and Sprint Performance in Youth Soccer: A Comparison of FIFA 11+ and RAMP Protocols","Comparative Effects of FIFA 11+ and RAMP Protocols on Agility and Sprint Performance Outcomes in Young Soccer Players","Inclusion Criteria:\n\n* Male, aged 8-15 years.\n* Minimum one year of organized soccer experience.\n* Currently training at least three times per week.\n* Willingness to participate and provide informed consent.\n\nExclusion Criteria:\n\n* Cardiovascular, neurological, or musculoskeletal disorders.\n* Musculoskeletal injury in the past six months.\n* Participation in other structured injury prevention or strength programs.\n* Inability to complete baseline testing.","MALE",{"count":81,"type":20},34,[23],"This randomized clinical trial investigates the comparative effects of the FIFA 11+ and RAMP (Raise, Activate, Mobilize, Potentiate) warm-up protocols on the agility and sprint performance of young soccer players. The study involves 34 male players aged 8 to 15, who will be randomly assigned to one of the two warm-up groups for a six-week intervention period. Key performance outcomes-agility, measured by the Illinois Agility Test, and sprint speed, measured by a 30-meter sprint test-will be assessed both before and after the intervention. The research aims to address a gap in sports science by directly comparing these two popular protocols in a youth population, with the goal of providing coaches with clear, evidence-based recommendations for optimizing athlete development and reducing injury risk. Data will be analyzed through SPSS version 27.00.",[27],[86,87,88,89,90,91],"Youth soccer","Warm-up protocols","FIFA 11+","RAMP","Agility","Sprint","2025-11-17",{"date":94,"type":36},"2025-11-24",{"date":96,"type":36},"2025-10-22",{"date":98,"type":20},"2026-06-16",{"name":71,"class":43},{"id":101,"slug":102,"hasResults":11,"nctId":103,"briefTitle":104,"officialTitle":105,"acronym":106,"eligibilityCriteria":107,"healthyVolunteers":11,"sex":16,"minAge":108,"maxAge":109,"enrollmentInfo":110,"targetDuration":4,"studyType":112,"phases":4,"briefSummary":113,"conditions":114,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":117,"lastUpdatePostDateStruct":118,"startDateStruct":120,"completionDateStruct":122,"leadSponsor":124,"locationsCount":44},"100443547","opportunistic-pkpd-trial-in-critically-ill-children-optic-100443547","NCT05055830","Opportunistic PK\u002FPD Trial in Critically Ill Children (OPTIC)","Clinically Integrated Opportunistic PK\u002FPD Trial in Critically Ill Children","OPTIC","Inclusion Criteria:\n\nTo be eligible for enrollment, a potential participant must meet all the following criteria:\n\n1. Participant is \\\u003C21 years old on admission\n2. Participant is admitted to the Pediatric Cardiac Intensive Care Unit\n3. Parent\u002Flegal guardian\u002Fadult participant can understand the consent process and is willing to provide informed consent\u002Fassent\n4. Participant is receiving one or more of the study drugs of interest at the time of enrollment\n\nExclusion Criteria:\n\n1\\. Any condition which would make the participant, in the opinion of the investigator, unsuitable for the study","0 Months","20 Years",{"count":111,"type":20},2000,"OBSERVATIONAL","OPTIC is a prospective, open-label, non-randomized study of multiple medications administered to approximately 2000 children in the pediatric cardiac intensive care unit (PCICU) per routine clinical car by their treating provider. The purpose of this study is to characterize the PK of drugs routinely administered to children per standard of care using opportunistic and scavenged samples. The prescribing of drugs to children will not be part of this protocol.\n\nAfter the child\u002Fadult (\\\u003C21 years of age) is consented\u002Fenrolled, demographic and clinical data will be extracted from the EHR. Biospecimen information (including date and time of sample collection) will be collected.\n\nData analysis will be conducted on all participants with at least 2 evaluable samples. The protocol represents minimal risk to the children\u002Fadults who provide body fluid for this study, including potential loss of confidentiality (samples will be assigned a unique accession number) and risks associated with blood draws. Adverse Events (AEs)\u002FSerious Adverse Events (SAEs) caused by the study specimen collections will be monitored and recorded in the Electronic Data Capture (EDC) system.",[115,116,27],"Cardiac Disease","Critically Ill","2025-11-13",{"date":119,"type":36},"2025-11-14",{"date":121,"type":36},"2021-10-05",{"date":123,"type":20},"2028-10-30",{"name":125,"class":43},"Duke University"]