[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"disabilities-multiple\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:disabilities-multiple":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,47,79,110,131],{"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":24,"studyType":25,"phases":4,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100562868","end-diagnostic-overshadowing-100562868",false,"NCT06608758","End Diagnostic Overshadowing","End Diagnostic Overshadowing: Understanding and Reducing Diagnostic Error in Patients With Disabilities","EDO","Inclusion Criteria:\n\n• Patients aged 3-89 who received billed charges\n\nExclusion Criteria:\n\n* Patients under age 3 or over age 89.\n* Patients with secondary diagnosis of dementia as the population is already known to be at increased risk of diagnostic error",true,"ALL","3 Years","89 Years",{"count":22,"type":23},120000,"ESTIMATED","4 Years","OBSERVATIONAL","The goal of this study is to address the critical issue of diagnostic overshadowing by applying the Collective Impact Model40 to co-produce our End Diagnostic Overshadowing program with academic, health systems, health professional, PWDs, family members, and community stakeholders. Through this work, we will identify and address mechanisms that contribute to diagnostic overshadowing and diagnostic errors among people with disabilities. The main questions to answer are whether knowledge about diagnostic errors and confidence will improve with health care providers and professionals involved in diagnostic provesses, whether developed algorithms to identify patients at risk of diagnpstic error will be used, whether there will be change in time to diagnostic evaluation for PWD from the specified 5 population groups and with the specified diagnoses prone to error, and whether changes in usage of CPT Evaluation and Management codes will occur.",[28],"Disabilities Multiple",[30,31,32,33],"Disabilities","Diagnostic error","Diagnostic overshadowing","Algorithms","RECRUITING","2026-08-03",{"date":37,"type":38},"2026-08-05","ACTUAL",{"date":40,"type":38},"2024-11-22",{"date":42,"type":23},"2029-07-31",{"name":44,"class":45},"Rush University Medical Center","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":17,"sex":54,"minAge":55,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":58,"phases":59,"briefSummary":61,"conditions":62,"keywords":65,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":46},"100645887","training-on-the-heimlich-maneuver-for-mothers-of-children-with-disabilities-100645887","NCT07699341","Training on the Heimlich Maneuver for Mothers of Children With Disabilities","For a Safe Breath: Training on the Heimlich Maneuver for Mothers of Children With Disabilities in Cases of Foreign Body Obstruction","Inclusion Criteria:\n\n1. Be a mother of a child with a disability, aged 1-8, who is enrolled in a rehabilitation center.\n2. Be 18 years of age or older.\n3. Be able to read and understand the research protocol, provide written informed consent, and agree to participate.\n4. Be physically able to participate in the training (standing\u002Fmodel-based exercises).\n\nExclusion Criteria:\n\n1. Must have previously received professional Heimlich maneuver\u002Ffirst aid training (those who have taken a course within the last 2 years).\n2. Those who are unable to participate in hands-on training due to physical limitations (e.g., severe heart disease, mobility issues).\n3. Individuals determined to be unsuitable for training or assessments due to psychiatric or neurological conditions.\n4. Children with severe respiratory system disorders (e.g., tracheostomy, severe bronchopulmonary dysplasia),\n5. Children who have undergone heart surgery or have a serious cardiac anomaly,\n6. Children with severe orthopedic or neurological disabilities for whom performing the Heimlich maneuver may be risky,\n7. Children with congenital anomalies of the trachea or upper respiratory tract (e.g., tracheoesophageal fistula),\n8. Children requiring mechanical ventilator support or continuous oxygen therapy.\n9. Withdrawing from participation during the study or failing to attend any of the training\u002Ftesting sessions.","FEMALE","18 Years",{"count":57,"type":23},70,"INTERVENTIONAL",[60],"NA","Foreign body obstruction is one of the most common causes of medical emergencies, particularly in childhood, and can lead to fatal outcomes if not treated promptly and correctly. Therefore, this study aims to examine the effect of hands-on Heimlich maneuver training for mothers of children with disabilities on the mothers' knowledge, skills, self-efficacy, and anxiety levels. Conducted as a randomized controlled trial, the study is planned to include 70 mothers (experimental group: 35, control group: 35) of children aged 1-8 years attending a private rehabilitation center in the Besni district of Adıyaman. Data collection tools will consist of a demographic information form, a Heimlich maneuver knowledge and skill test, and self-efficacy and anxiety scales. A pilot study will be conducted to evaluate the validity and reliability of the data collection tools, test their comprehensibility for the mothers, and identify potential problems that may arise during implementation. Prior to the start of the training, the knowledge levels of all mothers will be assessed via a questionnaire. The Heimlich maneuver training provided to mothers in the experimental group will be delivered hands-on using a pediatric Heimlich mannequin. One month after the training, a post-test will be administered to the mothers. Mothers in the control group will be informed about the study during the initial interview and will take a pre-test. One month after the training, the mothers will take the post-test. Mothers in the control group will be informed about the study during the initial interview and will take the pre-test. The post-test will be administered one month later, after which the mothers in this group will also receive maneuver training. The mothers' pre-test and post-test scores will be compared both within and between groups.",[28,63,64],"Obstruction Airway","Foreign Body Aspiration",[66,67,30,68,69],"Breath","Foreign Body Obstruction","Children","Heimlich Maneuver","2026-07-09",{"date":72,"type":38},"2026-07-13",{"date":74,"type":38},"2016-06-01",{"date":76,"type":23},"2026-11-30",{"name":78,"class":45},"University of Yalova",{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":18,"minAge":87,"maxAge":55,"enrollmentInfo":88,"targetDuration":4,"studyType":58,"phases":90,"briefSummary":91,"conditions":92,"keywords":97,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":46},"100497792","pediatric-medication-therapy-management-trial-100497792","NCT05761847","Pediatric Medication Therapy Management Trial","Optimizing the Clinical Management of Polypharmacy for Children With Medical Complexity: The Pediatric Medication Therapy Management (pMTM) Trial","pMTM","Inclusion Criteria:\n\n* 2-18 years old\n* ≥1 complex chronic condition (CCC)\n* ≥5 current medications (including prescription, as needed, and over-the-counter medications)\n* Receives primary care at Children's Hospital Colorado\n\nExclusion Criteria:\n\n* Non-English speaking\n* Sibling or family member already enrolled in this study","2 Years",{"count":89,"type":23},371,[60],"The purpose of this study is to evaluate whether an intervention called Pediatric Medication Therapy Management (pMTM) improves the identification and management of medication-related problems among children with medical complexity and polypharmacy.",[93,28,94,95,96],"Child, Only","Medication Interaction","Medication Compliance","Medication Administered in Error",[98,99,100],"Children with Medical Complexity","Polypharmacy","Medication Safety","2026-04-27",{"date":103,"type":38},"2026-04-28",{"date":105,"type":38},"2023-09-11",{"date":107,"type":23},"2028-01-31",{"name":109,"class":45},"University of Colorado, Denver",{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":4,"eligibilityCriteria":116,"healthyVolunteers":11,"sex":18,"minAge":55,"maxAge":4,"enrollmentInfo":117,"targetDuration":4,"studyType":58,"phases":119,"briefSummary":120,"conditions":121,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":125,"completionDateStruct":127,"leadSponsor":129,"locationsCount":46},"100500176","improving-the-health-and-social-participation-of-people-with-disabilities-from-underrepresented-groups-post-covid-100500176","NCT05792852","Improving the Health and Social Participation of People With Disabilities From Underrepresented Groups Post COVID","Feasibility of ENGAGE to Address Social Isolation Related to the COVID-19 Pandemic","Inclusion Criteria:\n\n* Self-identify as disabled\n* Report problems with social participation\n* Speak English\n* Live in a community setting\n\nExclusion Criteria:\n\n* Severe communication impairment limiting ability to verbally indicate interest in participation",{"count":118,"type":23},21,[60],"This is a single-arm community-based feasibility study examining recruitment, retention, adherence, and satisfaction with ENGAGE, a community-based intervention designed to address pandemic-related social isolation among people with disabilities. We will also examine preliminary, within-group effects on social participation. The findings of this study will inform a larger trial to examine intervention efficacy.",[28],"2025-04-21",{"date":124,"type":38},"2025-04-24",{"date":126,"type":38},"2023-04-01",{"date":128,"type":23},"2026-01-31",{"name":130,"class":45},"University of Illinois at Chicago",{"id":132,"slug":133,"hasResults":11,"nctId":134,"briefTitle":135,"officialTitle":136,"acronym":4,"eligibilityCriteria":137,"healthyVolunteers":17,"sex":18,"minAge":138,"maxAge":139,"enrollmentInfo":140,"targetDuration":4,"studyType":25,"phases":4,"briefSummary":142,"conditions":143,"keywords":147,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":150,"lastUpdatePostDateStruct":151,"startDateStruct":153,"completionDateStruct":155,"leadSponsor":157,"locationsCount":46},"100524105","characteristics-of-injury-claims-by-chronic-pain-patients-100524105","NCT06104384","Characteristics of Injury Claims by Chronic Pain Patients","Socio-demographics of Injury Insurance Claims by Chronic Pain Patients","Inclusion Criteria:\n\n* adult chronic pain patients\n* patients with injury claim\n\nExclusion Criteria:\n\n* pediatric patients\n* patients without injury claim","20 Years","99 Years",{"count":141,"type":23},1000,"Chronic pain is associated with injuries and disabilities. This prospective observational study explores the injury or disability claims made by chronic pain patients. It evaluates the socio-demographics of the patient population. It explores the impact of pain clinic services on the patients' injury rehabilitation, insurance claim outcome, and socioeconomic situation.",[144,145,146,28],"Social Functioning","Chronic Pain","Injuries",[148,149],"Injury Claim","Disability Claim","2025-01-23",{"date":152,"type":38},"2025-01-27",{"date":154,"type":38},"2018-01-02",{"date":156,"type":23},"2025-12-31",{"name":158,"class":45},"Salem Anaesthesia Pain Clinic"]