[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"child-neglect\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:child-neglect":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,51,77,105,132,153,179,203,226],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":33,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100633071","child-abuse-and-neglect-awareness-training-in-nursing-students-100633071",false,"NCT07521917","Child Abuse and Neglect Awareness Training in Nursing Students","Effect of Child Abuse and Neglect Awareness Training on Nursing Students: A Randomized Controlled Trial","CANAT","Inclusion Criteria:\n\n* Being an undergraduate nursing student\n* Being able to read and understand Turkish\n* Willingness to participate in the study\n* Providing written informed consent\n\nExclusion Criteria:\n\n* Not completing the training program\n* Not completing the pre-test or post-test\n* Withdrawing from the study at any stage",true,"ALL","18 Years","30 Years",{"count":22,"type":23},120,"ESTIMATED","INTERVENTIONAL",[26],"NA","This randomized controlled study aims to evaluate the effect of a child abuse and neglect awareness training program on the knowledge and awareness levels of nursing students. Child abuse and neglect remain significant global public health issues, and healthcare professionals, particularly nurses, play a key role in early recognition and intervention.\n\nThe study will be conducted among undergraduate nursing students at a university in Istanbul, Turkey. Participants will be randomly assigned to either an experimental group or a control group. Both groups will complete a pre-test to assess baseline knowledge levels. The experimental group will receive a structured training program on child abuse and neglect delivered by an expert nurse working at a Child Advocacy Center under the Ministry of Health, while the control group will not receive any intervention during the study period.\n\nOne month after the intervention, both groups will complete a post-test to assess changes in knowledge and awareness levels. The primary outcome of the study is the difference in awareness test scores between the pre-test and post-test. The findings are expected to contribute to improving educational strategies and enhancing the competencies of future nurses in recognizing and managing child abuse and neglect cases.",[29,30,31,32],"Child Abuse","Child Neglect","Awareness","Nursing Education",[34,35,36,37],"Nursing students","Child abuse","Child neglect","Awareness training","NOT_YET_RECRUITING","2026-04-11",{"date":41,"type":42},"2026-04-15","ACTUAL",{"date":44,"type":23},"2026-04-01",{"date":46,"type":23},"2026-06-30",{"name":48,"class":49},"Istanbul Arel University","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":17,"sex":58,"minAge":19,"maxAge":4,"enrollmentInfo":59,"targetDuration":4,"studyType":24,"phases":61,"briefSummary":62,"conditions":63,"keywords":4,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":50},"100482478","a-regional-partnership-to-improve-outcomes-through-fatherhood-engagement-100482478","NCT05562557","A Regional Partnership to Improve Outcomes Through Fatherhood Engagement","A Regional Partnership for New York City to Improve Well-Being and Child Welfare Outcomes Among Families at Risk of Substance Misuse Through Fatherhood Engagement","Inclusion Criteria:\n\n* is a custodial or non-custodial father\n* speaks English or Spanish\n* has at least one child under the age of 18,\n* someone in the family is identified as at-risk for substance use through: self-report of illicit substance use in the family, the presence of an SUD diagnosis in the family, a clinician\u002Fprovider identified substance use risk, or the presence of a substance-related indicated child welfare allegation in the family\n\nExclusion Criteria:\n\n* The placement of all children in the family in foster care","MALE",{"count":60,"type":23},240,[26],"Montefiore will engage fathers in families at risk of substance misuse in the Bronx and neighboring communities. Families will be referred from Bronx and neighboring community-based child welfare systems, substance use disorder (SUD) treatment providers, and medical providers if identified at risk of substance use concerns and will be randomly assigned to receive services as usual as part of the comparison group, or to receive enhanced services as part of the program group.\n\nEnhanced services include: (1) Motivational Enhancement; (2) referral to Healthy, Empowered, Resilient, and Open (HERO) Dads fatherhood engagement program; (3) Contingency Management; and (4) Case Management.",[64,29,30,65,66],"Substance Use","Fathers","Father-Child Relations","RECRUITING","2026-03-19",{"date":70,"type":42},"2026-03-24",{"date":72,"type":42},"2023-05-09",{"date":74,"type":23},"2027-09",{"name":76,"class":49},"Montefiore Medical Center",{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":83,"eligibilityCriteria":84,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":85,"targetDuration":4,"studyType":24,"phases":87,"briefSummary":88,"conditions":89,"keywords":91,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":50},"100226430","ilookout-for-child-abuse--online-learning-module-for-early-childcare-providers-100226430","NCT02225301","iLookOut for Child Abuse -Online Learning Module for Early Childcare Providers","Early Childhood Practitioner's Knowledge and Attitudes Regarding Reporting Child Abuse\u002FNeglect-iLookOut","iLookOut","Inclusion Criteria:\n\n* Paid or volunteer staff at childcare facility\n\nExclusion Criteria:\n\n* Younger than 18 years of age",{"count":86,"type":23},35000,[26],"Phase 1 was a randomized control trial that used a test-retest model to evaluate the impact of iLook Out for Child Abuse, an online, interactive learning module about reporting suspected child abuse. Delivered via a learning management system to early childhood professionals who work with infants and young children, this study assessed iLookOut's effect on 1) knowledge about reporting suspected child abuse; 2) attitudes toward reporting suspected child abuse; and 3) preparedness to protect children at risk.\n\nFindings from Phase 1 were that iLookOut will improved knowledge, changed attitudes, and increase self-reported preparedness of early childhood providers to report suspected child abuse.\n\nPhase 2 of this trial is an open-enrollment study that records pre-\u002Fpost- data on the same measurements as Phase 1, and is available for use (free of charge) for all childcare providers in Pennsylvania at https:\u002F\u002Fwww.ilookoutforchildabuse.com.",[29,30,90],"Child Maltreatment",[92,93,94,95],"Child maltreatment","Child Care","Knowledge","Attitude","2026-01-23",{"date":98,"type":42},"2026-01-26",{"date":100,"type":42},"2014-11-01",{"date":102,"type":23},"2028-12-31",{"name":104,"class":49},"Milton S. Hershey Medical Center",{"id":106,"slug":107,"hasResults":11,"nctId":108,"briefTitle":109,"officialTitle":109,"acronym":4,"eligibilityCriteria":110,"healthyVolunteers":11,"sex":18,"minAge":111,"maxAge":19,"enrollmentInfo":112,"targetDuration":4,"studyType":114,"phases":4,"briefSummary":115,"conditions":116,"keywords":117,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":130,"locationsCount":50},"100498646","children-at-risk-and-oral-health-the-dental-record-study-100498646","NCT05772962","Children at Risk and Oral Health, The Dental Record Study","Inclusion Criteria:\n\n* Children enrolled at CAC\n* Control group matched by age and gender\n\nExclusion Criteria:\n\n* Children with developmental disorders that affect oral health\n* Children with mental retardation","0 Years",{"count":113,"type":23},2400,"OBSERVATIONAL","The objectives of this retrospective dental record study, are to increase knowledge of the oral health, - history and -needs of children enrolled at the Childrens Advocacy Centers (CAC)by:\n\n* assessing if it is possible to identify oral indicators of child maltreatment.\n* assessing if and to what degree the children enrolled at CAC are in need of close, adapted and trauma sensitive treatment and follow up at the Public Dental Health Service (PDHS)\n* assessing if there is a need for new routines in terms of interdisciplinary collaboration and sharing of information between CAC, Child Welfare Services (CWS) and PDHP.\n\nBy increasing knowledge in regard to child maltreatment and oral health, the study will raise PDHS and CAC ability to prevent, detect and help children being victims of maltreatment, and contribute to strengthen PDHS, CAC and CWS interdisciplinary interaction for the benefit of children at risk.",[29,30,90],[118,119,120,121,122,123],"Oral health","Dental health service","Childrens advocacy center","Prevention","Detection","Collaboration","2026-01-12",{"date":126,"type":42},"2026-01-14",{"date":128,"type":42},"2024-12-05",{"date":102,"type":23},{"name":131,"class":49},"Oral Health Centre of Expertise in Western Norway",{"id":133,"slug":134,"hasResults":11,"nctId":135,"briefTitle":136,"officialTitle":137,"acronym":138,"eligibilityCriteria":139,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":140,"targetDuration":4,"studyType":114,"phases":4,"briefSummary":142,"conditions":143,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":144,"lastUpdatePostDateStruct":145,"startDateStruct":147,"completionDateStruct":149,"leadSponsor":151,"locationsCount":4},"100612168","sentinella-registry-and-training-for-child-protection-100612168","NCT07250074","\"Sentinella\": Registry and Training for Child Protection","\"Sentinella\" Project: a Digital Registry and Education Network for Child Maltreatment Protection.","Sentinella","Inclusion Criteria:\n\n* Healthcare professionals (e.g., pediatricians, psychologists, nurses, social workers) working within the regional pediatric network.\n* Voluntary participation in the Sentinella project.\n* Completion of the planned training program (theoretical and practical components).\n* Willingness to use the digital registry and complete evaluation questionnaires.\n* Provision of written informed consent.\n\nExclusion Criteria:\n\n* Failure to complete the full training program.\n* Partial participation in simulation or practical sessions.\n* Incomplete pre- and post-training questionnaires.\n* Refusal or withdrawal of informed consent.",{"count":141,"type":23},30,"The \"Sentinella\" project aims to improve the early recognition and prevention of child maltreatment by creating a digital registry and education network for healthcare professionals. The study will test a new online registry built on the REDCap platform to collect standardized, anonymous data about suspected cases of abuse or neglect. It also includes a structured training program for pediatricians and other healthcare workers to strengthen their skills in identifying and reporting maltreatment.\n\nThis observational study will assess how easy the registry is to use and whether the training improves participants' knowledge and reporting practices. The project is expected to enhance collaboration between hospitals and community services, reduce reporting delays, and create a model for regional or national systems to protect vulnerable children.",[29,30,90],"2025-11-18",{"date":146,"type":42},"2025-11-26",{"date":148,"type":23},"2025-12-03",{"date":150,"type":23},"2027-11-03",{"name":152,"class":49},"Buzzi Children's Hospital",{"id":154,"slug":155,"hasResults":11,"nctId":156,"briefTitle":157,"officialTitle":158,"acronym":4,"eligibilityCriteria":159,"healthyVolunteers":11,"sex":18,"minAge":160,"maxAge":161,"enrollmentInfo":162,"targetDuration":4,"studyType":114,"phases":4,"briefSummary":164,"conditions":165,"keywords":168,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":170,"lastUpdatePostDateStruct":171,"startDateStruct":173,"completionDateStruct":175,"leadSponsor":177,"locationsCount":50},"100569781","the-eeg-study-under-remimazolam-anesthesia-in-children-100569781","NCT06698705","The EEG Study Under Remimazolam Anesthesia in Children","Electroencephalogram Study in Children Under Remimazolam Anesthesia - a Prospective,Observational Study","Inclusion Criteria:\n\n1\\. aged 1 years-12 years; 2, with American Society of Anesthesiologists (ASA) physical status I or II; 3, children requiring general anesthesia under remimazolam; 4, parents or legal guardians of children who volunteered to participate in the trial; And signed the informed consent form.\n\nExclusion Criteria:\n\n1. Congenital malformation or other genetic conditions that are thought to affect brain development ;\n2. History of severe heart, brain, liver, kidney and metabolic diseases ;\n3. Premature infants (≤32 weeks);\n4. Upper respiratory tract infection in the last two weeks. -","1 Year","12 Years",{"count":163,"type":23},60,"The effect of Remimazolam on brain electrical activity. Previous studies have shown that in healthy male volunteers, EEG changes during Remimazolam infusion are characterized by an initial increase in the beta band and a later increase in the delta band. When monitoring the depth of anesthesia, the commonly used Bispectral Index in clinical practice was originally developed for propofol. Therefore, studies have shown that the correlation between the depth of sedation of benzodiazepines such as midazolam and Bispectral Index is weak. In contrast, the beta wave ratio is considered a more suitable EEG indicator for monitoring the sedative effect of Remimazolam. The above indicates that Remimazolam has a specific pattern of influence on EEG activity, especially in the regulation of anesthesia depth, with unique characteristics.",[166,167,30],"Electroencephalography","Remimazolam",[166,167,169],"children","2025-02-04",{"date":172,"type":42},"2025-02-06",{"date":174,"type":42},"2024-11-22",{"date":176,"type":23},"2025-12-01",{"name":178,"class":49},"Second Affiliated Hospital of Wenzhou Medical University",{"id":180,"slug":181,"hasResults":11,"nctId":182,"briefTitle":183,"officialTitle":184,"acronym":4,"eligibilityCriteria":185,"healthyVolunteers":17,"sex":18,"minAge":186,"maxAge":187,"enrollmentInfo":188,"targetDuration":4,"studyType":114,"phases":4,"briefSummary":190,"conditions":191,"keywords":193,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":170,"lastUpdatePostDateStruct":196,"startDateStruct":198,"completionDateStruct":200,"leadSponsor":202,"locationsCount":50},"100560659","the-eeg-study-under-sevoflurane-anesthesia-in-children-100560659","NCT06580028","The EEG Study Under Sevoflurane Anesthesia in Children","Electroencephalogram Study in Children Under Sevoflurane Anesthesia - a Prospective,Observational Study","Inclusion Criteria:\n\n1. aged 1 days#6 years#;\n2. with American Society of Anesthesiologists (ASA) physical status I or II#;\n3. children requiring general anesthesia under sevoflurane;\n4. parents or legal guardians of children who volunteered to participate in the trial; And signed the informed consent form.\n\nExclusion Criteria:\n\n1. Congenital malformation or other genetic conditions that are thought to affect brain development ;\n2. History of severe heart, brain, liver, kidney and metabolic diseases ;\n3. Premature infants (≤32 weeks);\n4. Upper respiratory tract infection in the last two weeks.","1 Day","6 Years",{"count":189,"type":23},280,"Sevoflurane is one of the most commonly used volatile anesthetics in children because of its rapid induction, recovery and recovery properties. Clinical studies using noninvasive brain monitoring have shown that general anesthetics and hypnotics generate electroencephalogram (EEG) oscillations in specific spatial tissues that are fundamentally related to the structure and function of neural circuits. Slow-wave-delta (0.1-4 Hz) oscillations were present in children of all ages, and the advantage of frontal α-wave oscillations appeared at approximately 6 months, began to be consistent at 10 months, and persisted at older ages. Another study, which analyzed EEG under sevoflurane general anesthesia in children aged 0-6 months, found that Theta and alpha wave power decreased with a decrease in sevoflurane concentrations in infants between 4 and 6 months of recovery. However, these studies lack detailed characterization of the neural circuit activity associated with anesthesia, especially at specific developmental ages that are highly correlated with brain plasticity. The aim of this study was to explore electroencephalogram (EEG) of children of different ages under sevoflurane general anesthesia (including anesthesia induction, maintenance and recovery) . By analyzing these EEG data in detail, we hope to be able to better understand the EEG characteristics of children of different ages under sevoflurane anesthesia, and thus develop a neurophysiology pediatric anesthesia status monitoring strategy.",[166,192,30],"Sevoflurane",[192,194,195],"Children","Electroencephalogram",{"date":197,"type":42},"2025-02-07",{"date":199,"type":42},"2024-09-04",{"date":201,"type":23},"2026-09",{"name":178,"class":49},{"id":204,"slug":205,"hasResults":11,"nctId":206,"briefTitle":207,"officialTitle":207,"acronym":4,"eligibilityCriteria":208,"healthyVolunteers":11,"sex":18,"minAge":4,"maxAge":209,"enrollmentInfo":210,"targetDuration":4,"studyType":24,"phases":212,"briefSummary":213,"conditions":214,"keywords":4,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":217,"lastUpdatePostDateStruct":218,"startDateStruct":220,"completionDateStruct":222,"leadSponsor":224,"locationsCount":50},"100397736","substance-use-treatment-and-access-to-resources-stars-project-100397736","NCT04459000","Substance Use Treatment and Access to Resources (STARS) Project","Inclusion Criteria:\n\n* Pregnant woman with substance abuse issue occurring during pregnancy\n* Eligible for services at the STAR prenatal clinic\n* Speaks\u002Fcomprehends English\n\nExclusion Criteria:\n\n* Unable to read English at 8th grade comprehension level\n* Those outside of Oklahoma City metropolitan area.","55 Years",{"count":211,"type":23},242,[26],"This study is evaluating a randomized clinical trial and a quasi-experimental observational study combined. Pregnant women with substance abuse issues are referred to the Substance Use Treatment and Recovery (STAR) prenatal clinic, and those who consent to participate in the study will be randomized to the STAR + maternal Attachment Biobehavioral Catchup (mABC) home visiting model or to the STAR only treatment group. Those who opt out of receiving prenatal care at STAR will be recruited as a control group for the QED portion. Those randomized to STAR + mABC will receive additional supports from a licensed therapist, including up to 12 home visits focused on substance exposed babies and positive parenting.",[215,216,30],"Substance Use Disorders","Pregnancy Related","2024-10-30",{"date":219,"type":42},"2024-10-31",{"date":221,"type":42},"2020-12-16",{"date":223,"type":23},"2025-09",{"name":225,"class":49},"University of Oklahoma",{"id":227,"slug":228,"hasResults":11,"nctId":229,"briefTitle":230,"officialTitle":231,"acronym":4,"eligibilityCriteria":232,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":233,"targetDuration":4,"studyType":24,"phases":235,"briefSummary":236,"conditions":237,"keywords":241,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":244,"lastUpdatePostDateStruct":245,"startDateStruct":247,"completionDateStruct":249,"leadSponsor":251,"locationsCount":4},"100562205","screening-to-identify-parents-in-need-of-mental-health-support-a-feasibility-study-in-child-welfare-services-100562205","NCT06600139","Screening to Identify Parents in Need of Mental Health Support: a Feasibility Study in Child Welfare Services","A Feasibility Study of the Collaboration-Screening-Referral Model - an Approach to Identify Parents in Child Welfare Services Who Need Mental Health Support","SOCIAL WORKERS:\n\nInclusion Criteria:\n\n* Working at the participating units.\n\nExclusion Criteria:\n\n* None.\n\nPARENTS:\n\nInclusion Criteria:\n\n* A parental role in relation to a child 0-17 years old (the participant does need not be a guardian or biological parent, can also be, for example, a partner to a parent).\n* A child welfare report has been filed for the child or the parent has reached out to the CWS themselves.\n\nExclusion Criteria:\n\n* None.",{"count":234,"type":23},355,[26],"The main aim of this study is to evaluate the feasibility, preliminary effects and experiences of the Collaboration-Screening-Referral approach (in Swedish: Samverkan-Screening-Hänvisning - SSH) when used with parents referred to the Swedish child welfare services. The SSH is an approach to screen parents for symptoms of mental illness using structured questionnaires, establish intra-agency collaboration, and refer to mental health services. Additionally, to increase social workers\\' competence in assessing and handling mental illness through receiving training in the SSH and administering the screening to parents.\n\nThe main questions the project aims to answer are:\n\n* Are parents engaged with child welfare services willing to undergo screening for symptoms of depression and anxiety?\n* How have the implementation of the SSH proceeded and to what degree is it sustained?\n* How do parents and social workers experience the SSH?\n* Do social workers' behaviors, knowledge and competence relevant to supporting parents with mental illness increase when implementing the SSH?\n\nSocial workers answer questions before and after their training and after 6 and 12 months. Additionally, social workers and parents will be interviewed. Qualitative and quantitative within-group analyses will be conducted to examine experiences and preliminary effects of the SSH.",[238,239,240,29,30,90],"Mental Disorder","Depression","Anxiety",[242,243,90,239,240],"Parenting","Screening","2024-09-13",{"date":246,"type":42},"2024-09-19",{"date":248,"type":23},"2024-09-20",{"date":250,"type":23},"2025-09-30",{"name":252,"class":49},"Karolinska Institutet"]