[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"exposure\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:exposure":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,52,92,119,173],{"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":4,"briefSummary":24,"conditions":25,"keywords":34,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":4},"100613748","french-military-firefighters-to-assess-relationships-between-exposome-and-health-100613748",false,"NCT07270627","French Military Firefighters to Assess Relationships Between Exposome and Health.","Cohorte Militaire et Son Exposome : étude Pilote rétrospective au Sein de la Population Des Sapeurs-pompiers (Actuellement en Exercice et Anciens Sapeurs-pompiers) de la Brigade Des Sapeurs Pompiers de Paris","COMITEX-BSPP","Inclusion Criteria:\n\n* Active-duty or veteran military personnel from French Paris firefighter brigade.\n* Aged at least 18.\n* Not opposed to participate to the study\n\nExclusion Criteria:\n\n* Opposition to participate\n* veterans under legal protection",true,"ALL","18 Years",{"count":21,"type":22},15000,"ESTIMATED","OBSERVATIONAL","The aim of the study is to describe professional exposures and health events among French military firefighters (both active-duty personnel and veterans) and identify potential relationships between the exposome (the total history of occupational and personal exposures) and health status in these populations. The study is based on a self-administered questionnaire that collects retrospective and present information about exposures and health conditions.",[26,27,28,29,30,31,32,33],"Health Adult Subjects","Exposure Occupational","Health Behavior, Risky","Occupational Health","Exposure","Firefighters","Military Personnel","Observational Study",[35,36,37,38,39],"Occupational exposure","health","military","exposome","occupational","NOT_YET_RECRUITING","2025-11-26",{"date":43,"type":44},"2025-12-08","ACTUAL",{"date":46,"type":22},"2026-01-01",{"date":48,"type":22},"2026-12",{"name":50,"class":51},"Direction Centrale du Service de Santé des Armées","OTHER",{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":4,"eligibilityCriteria":58,"healthyVolunteers":17,"sex":18,"minAge":59,"maxAge":60,"enrollmentInfo":61,"targetDuration":4,"studyType":63,"phases":64,"briefSummary":66,"conditions":67,"keywords":74,"overallStatus":81,"whyStopped":4,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":91},"100598556","how-digital-media-affects-kids-healthcare-experiences-and-outcomes-100598556","NCT07073027","How Digital Media Affects Kids' Healthcare Experiences and Outcomes","Evaluating the Impact of Digital Media on Patient-Reported Experience and Outcomes in Pediatrics","Inclusion Criteria:\n\n* Between the ages of 5 to 23\n* Able to follow instructions and communicate in English\n* Own or have access to a smartphone\n* Scheduled for an upcoming (approved) procedure.\n\nExclusion Criteria:\n\n* Under the age of 5 or older than 23\n* Vision, hearing, cognitive, and\u002For motor impairments\n* Cannot follow instructions and\u002For communicate in English\n* Do not own or have access to a smartphone.","5 Years","23 Years",{"count":62,"type":22},500,"INTERVENTIONAL",[65],"NA","The goal of this clinical trial is to learn whether different forms of media (2D, 360, or 360 in virtual reality) have different impacts on pre-procedural anxiety and post-procedural pain in children. The main questions it aims to answer are:\n\nDoes one type (and richness) of media reduce pre-procedural anxiety and post-procedural pain more than another type of media? For example, will learning about an upcoming procedure by watching a 360 video in virtual reality reduce pre-procedural anxiety more than learning about the same upcoming procedure by watching it in a 2D video or 360 video?\n\nThe second question is whether watching a 360 video in VR about an upcoming procedure more effective in reducing pre-procedural anxiety and post-procedural pain compared to the 2D video or the 360 video without VR groups for specific procedures? For example, is watching an explanation of a procedure in VR always more effective in reducing pre-procedural anxiety and post-procedural pain, or is it procedure specific (i.e., watching a video about surgery preparation is more effective in VR, but for cast removal it doesn't matter whether participants learn about their procedure viewed through VR, 360 video, or 2D)?",[68,69,70,71,72,30,73],"Children","Adolescent","Anxiety","Pain","Education","Virtual Reality",[75,76,77,78,79,80],"pre-procedural anxiety","exposure therapy","virtual reality","education","children and adolescents","gamification","RECRUITING","2025-07-09",{"date":84,"type":44},"2025-07-18",{"date":86,"type":22},"2025-07",{"date":88,"type":22},"2026-03",{"name":90,"class":51},"British Columbia Children's Hospital",1,{"id":93,"slug":94,"hasResults":11,"nctId":95,"briefTitle":96,"officialTitle":97,"acronym":98,"eligibilityCriteria":99,"healthyVolunteers":11,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":100,"targetDuration":4,"studyType":63,"phases":102,"briefSummary":103,"conditions":104,"keywords":106,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":110,"lastUpdatePostDateStruct":111,"startDateStruct":113,"completionDateStruct":115,"leadSponsor":117,"locationsCount":91},"100580298","evaluate-a-local-program-to-reduce-the-risky-use-of-screens-by-children-under-3-based-on-the-experience-of-parents-who-successfully-stopped-this-exposure-100580298","NCT06835478","Evaluate a Local Program to Reduce the Risky Use of Screens by Children Under 3, Based on the Experience of Parents Who Successfully Stopped This Exposure.","Evaluate a Local Program to Reduce the Risky Use of Screens by Children Under 3, Based on the Experience of Parents Who Successfully Stopped This Exposure (EPURE)","EPURE","Inclusion Criteria:\n\n* Live in Saint-Denis (France)\n* Parent(s) of child(ren) for whom the family has declared that they have succeeded in stopping or totally modifying their behaviour with screens before the child's 3rd birthday (standard form for all health record follow-up examinations).\n* Declaration confirmed by the negativation of the SCREEN result calculated a posteriori for two periods (before and after stopping), at least 3 months apart.\n* No objection to the use of data for research purposes.\n\nExclusion Criteria:\n\n* Non-French-speaking public\n* Severe neurological or sensory disorder in the child\n* Child in alternating custody with difficulty accessing screen exposure in the other custody arrangement.\n* Refusal to use data",{"count":101,"type":22},290,[65],"Early exposure to screens puts children at risk of later neurodevelopmental delay. This exposure is particularly prevalent among the underprivileged populations in our study area, and we don't yet know the motivations, factors and constraints that need to be put in place to remedy the situation.\n\nOur approach is a bottom-up study, based on the experience of parents who stopped their child's exposure to screens before age 3, to develop a program to reduce early exposure to screens. This will then be tested on a larger scale via a randomized trial",[30,105],"Child Development",[107,108,109],"screens","screens exposure","child Development","2025-02-17",{"date":112,"type":44},"2025-02-19",{"date":114,"type":22},"2025-04-01",{"date":116,"type":22},"2027-02-01",{"name":118,"class":51},"Centre Hospitalier de Saint-Denis",{"id":120,"slug":121,"hasResults":11,"nctId":122,"briefTitle":123,"officialTitle":123,"acronym":124,"eligibilityCriteria":125,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":126,"enrollmentInfo":127,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":129,"conditions":130,"keywords":139,"overallStatus":81,"whyStopped":4,"lastUpdateSubmitDate":163,"lastUpdatePostDateStruct":164,"startDateStruct":166,"completionDateStruct":168,"leadSponsor":170,"locationsCount":172},"100540952","cohort-study-on-plant-based-diets-coplant-study-100540952","NCT06323538","Cohort Study on Plant-based Diets (COPLANT Study)","COPLANT","Inclusion Criteria:\n\n* age between 18 and 69 years at recruitment (age-stratified recruitment in four age groups (18 to 29, 30 to 39, 40 to 49 and 50 to 69 years) which should be equally distributed across the four diets)\n* following their current diet for at least one year\n* health insured\n* are willing to have blood taken (adults)\n* are willing and able to complete questionnaires\n* only at Berlin, Jena, Giessen and Karlsruhe sites: pregnant and breastfeeding women were recruited (shortened examination programm)\n* only at the Regensburg, Heidelberg, Bonn and Vienna sites: are neither pregnant nor breastfeeding at the time of recruitment\n* only at Berlin and Karlsruhe sites: children of adult participants (shortened examination programm without collection of blood, urine, and stool)\n* are able to give informed consent to participate in the study\n* have given their consent to participate in the COPLANT study\n\nExclusion Criteria:\n\n* who can no longer be contacted\n* who withdraw their consent to participate in the study","69 Years",{"count":128,"type":22},6000,"The Cohort on Plant-based Diets (COPLANT) study is a multi-centre cohort study that starts baseline recruitment from 2024 to 2027 with approximately 6,000 participants in Germany and Austria. The COPLANT study focuses on vegan (no animal products), vegetarian (no meat and fish, but dairy products and eggs), pescetarian (no meat, but fish) and omnivorous (mixed diet including all possible animal products) diets. The aim of the COPLANT study is to gain new insights on health benefits and risks as well as social, ecological and economic effects of different plant-based diets in comparison to a mixed diet. In addition to a detailed dietary survey using an app adapted to the needs of this study, the baseline examination includes measurements of body composition, bone health, cardiovascular risk factors, diabetes risk, contaminants and lifestyle. For the basic laboratory program, fasting blood, 24-hour urine collection and a stool sample are taken from all study participants. Furthermore, specific aspects of dietary behavior, physical activity and other lifestyle factors are collected via questionnaires. Follow-up studies are planned at intervals of 5, 10 and 20 years after the baseline visit.",[131,132,133,134,135,30,136,137,138],"Dietary Exposure","Diabetes Mellitus, Type 2","Cardiovascular Diseases","Bone Loss","Sustainability","Obesity","Vitamin Deficiency","Mineral Deficiency",[140,141,142,143,144,145,146,147,148,149,150,151,152,153,154,155,156,157,158,159,160,161,162],"vegan","vegetarian","pescetarian","omnivor","multicenter cohort","biomarker","vitamins","minerals","bone health","cardiovascular risk","body composition","inflammation","contaminants","diabetes type 2","thyroid gland health","microbiota","metabolomics","adults","children","pregnancy","breast feeding time","mental health","sustainability","2025-02-13",{"date":165,"type":44},"2025-02-14",{"date":167,"type":44},"2024-04-09",{"date":169,"type":22},"2047-03-31",{"name":171,"class":51},"German Federal Institute for Risk Assessment",8,{"id":174,"slug":175,"hasResults":11,"nctId":176,"briefTitle":177,"officialTitle":177,"acronym":4,"eligibilityCriteria":178,"healthyVolunteers":11,"sex":18,"minAge":179,"maxAge":19,"enrollmentInfo":180,"targetDuration":4,"studyType":63,"phases":182,"briefSummary":183,"conditions":184,"keywords":187,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":191,"lastUpdatePostDateStruct":192,"startDateStruct":194,"completionDateStruct":196,"leadSponsor":198,"locationsCount":4},"100542125","one-session-virtual-reality-during-ongoing-treatment-for-anxiety-feasibility-in-children-and-adolescents-100542125","NCT06338800","One Session Virtual Reality During Ongoing Treatment for Anxiety: Feasibility in Children and Adolescents","Inclusion Criteria:\n\n* Children and adolescents 8-18 years old.\n* Meeting Diagnostic and Statistical Manual of Mental Disorders -5 criteria for an anxiety disorder, based on a semi-structured interview (SCID-5 Jr, specific section) or clinical judgment of an experienced and authorized clinician.\n\nExclusion Criteria:\n\n* Severe psychiatric symptoms other than anxiety disorder interfering with safety or warranting immediate intervention, e.g. psychosis or acute suicidality.","8 Years",{"count":181,"type":22},30,[65],"The goal of this study is to evaluate one session with exposure with Virtual Reality (VR) in in children and adolescents, aged 8-18 years with an anxiety disorder. The main questions it aims to answer are:\n\n1. What are the expectations of children and adolescents and therapists with VR exposure?\n2. What is the acceptability of the VR session (positive and negative effects)?\n3. What are possible working mechanisms of VR exposure? During ongoing treatment, participants will receive a session of exposure with VR.",[185,30,186],"Anxiety Disorders","Social Anxiety Disorder",[68,188,189,190],"Adolescents","Virtual Reality Exposure","Anxiety disorders","2024-08-14",{"date":193,"type":44},"2024-08-15",{"date":195,"type":22},"2024-09",{"date":197,"type":22},"2025-12",{"name":199,"class":51},"Accare"]