[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"risk-reduction-behavior\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:risk-reduction-behavior":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,54,91,128,161,188],{"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":41,"whyStopped":4,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":50,"locationsCount":53},"100547896","driver-education-research-study-100547896",false,"NCT06413927","Driver Education Research Study","A Contemporary Look at Driver Training and Its Role in Reducing Crash Risk in Novice Adolescent Drivers","DRIVER","Inclusion Criteria:\n\n* Adolescents ages 16-17 years old who reside in Pennsylvania\n* Have an active Pennsylvania learner's permit\n* Have \\\u003C30 hours of driving practice during permit phase\n* Have never taken an on-road licensing exam, in any state\n* Plan to get a license within the next 12 months in Pennsylvania\n* Plan to have access to a vehicle to drive after licensure\n* Have a personal cell phone and access to a smartphone\u002Ftablet\u002Fcomputer with internet access\n* Download and use the RoadReady app (only required for participants randomized to the behind-the-wheel training arm; optional for participants randomized to the online vehicle and driver safety and online driver skills training arms)\n* Are able to read\u002Fwrite in English\n* Provide informed consent\u002Fassent\n* Are not also taking part in another learner driver study\n\nExclusion Criteria:\n\n* Non-Pennsylvania resident\n* Participants who do not pass the license exam will not be able to complete the post-license monitoring until the license is obtained\n* Enrolled in another learner driver study",true,"ALL","16 Years","17 Years",{"count":22,"type":23},1300,"ESTIMATED","INTERVENTIONAL",[26],"NA","This study will test the effectiveness of different types of driver training interventions for reducing young new driver crash risk early after licensure.",[29,30,31,32],"Risk Reduction Behavior","Injuries","Accident, Traffic","Development, Adolescent",[34,35,36,37,38,39,40],"Injury prevention","Adolescent development","Learner drivers","Crash risk reduction","Novice drivers","Risky Driving","Teens","RECRUITING","2026-03-31",{"date":44,"type":45},"2026-04-06","ACTUAL",{"date":47,"type":45},"2024-08-08",{"date":49,"type":23},"2027-12",{"name":51,"class":52},"Children's Hospital of Philadelphia","OTHER",1,{"id":55,"slug":56,"hasResults":11,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":4,"eligibilityCriteria":60,"healthyVolunteers":17,"sex":18,"minAge":61,"maxAge":4,"enrollmentInfo":62,"targetDuration":4,"studyType":24,"phases":64,"briefSummary":65,"conditions":66,"keywords":72,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":53},"100615004","life-skills-training-for-soldiers-arriving-at-their-first-duty-location-100615004","NCT07286955","Life Skills Training for Soldiers Arriving at Their First Duty Location","SAFEGUARD: Life Skills Training for Soldiers Arriving at Their First Duty Location","Inclusion Criteria:\n\n* Active duty Soldiers arriving at a military installation located in the South Central U.S. for their first duty location who are attending reception center activities\n\nExclusion Criteria:\n\n* Soldiers who are not available to attend the in-person training\n* Soldiers who are under the age of 18 years old\n* Soldiers who do not have a smart phone that supports installation of the mobile app","18 Years",{"count":63,"type":23},5000,[26],"This project will evaluate the effectiveness of Level Up: Boost Your Life Skills (\"Level Up\"), a strengths based, military-specific life skills training program. The goal is to determine whether Level Up can decrease suicidal-related behaviors (SRBs) and other harmful behaviors, improve mental health, enhance job performance, and reduce early military separation. The Level Up program components will be made available to participants through an online platform or mobile app that can be downloaded onto their personal mobile devices. These training materials will help Soldiers learn and practice skills. The Level Up program will also involve personalized messages from a Level Up trainer and virtual booster sessions. Soldiers arriving at their first duty location will be randomized to receive either Level Up or a single session Army bystander intervention program. Participants will complete baseline and follow up surveys 1, 3, and 6 months post-baseline.",[29,67,68,69,70,71],"Suicide Prevention","Risky Behavior","Mental Health","Resilience","Performance at Work",[73,67,74,75,76,77,78,79,80],"Military Health","Harmful Behaviors","Life Skills Training","First Duty Location","Active-duty Military","Risk Reduction","Prevention","Level Up","2026-01-09",{"date":83,"type":45},"2026-01-13",{"date":85,"type":45},"2025-12-10",{"date":87,"type":23},"2029-07-01",{"name":89,"class":90},"Uniformed Services University of the Health Sciences","FED",{"id":92,"slug":93,"hasResults":11,"nctId":94,"briefTitle":95,"officialTitle":96,"acronym":97,"eligibilityCriteria":98,"healthyVolunteers":17,"sex":18,"minAge":61,"maxAge":4,"enrollmentInfo":99,"targetDuration":4,"studyType":24,"phases":101,"briefSummary":102,"conditions":103,"keywords":112,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":119,"lastUpdatePostDateStruct":120,"startDateStruct":122,"completionDateStruct":124,"leadSponsor":126,"locationsCount":53},"100594836","assessing-the-effectiveness-of-heat-adaptation-digital-messages-from-primary-care-providers-to-their-patients-on-the-change-in-behaviour-for-heatwave-related-preparedness-100594836","NCT07024628","Assessing the Effectiveness of Heat Adaptation Digital Messages From Primary Care Providers to Their Patients on the Change in Behaviour for Heatwave-related Preparedness","Heat Smart: Empowering Primary Care Providers to Safeguard Vulnerable Populations Against Extreme Heat","HeatSmart","Inclusion Criteria:\n\nThe Heat Smart randomized controlled trial study will recruit patients and primary care providers (PCPs) from Eastern Ontario. The inclusion criteria ensure that the intervention reaches at-risk individuals while being scalable across different patient populations:\n\nPrimary Care Patients:\n\n* Adults (18 years and older)\n* Patients must be registered with a participating PCP.\n* They must have had at least one visit with their PCP in the past two years to ensure active engagement.\n* Participants must have an active email, cell phone or messaging service (SMS) to receive Heat Smart digital messages.\n* Patients must be able to understand and consent to participate in the study.\n* Patients must be able to communicate in at least one of the official languages (English, French).\n* Participants will be recruited from PCP located in two Eastern Ontario public health districts: the Eastern Ontario Health Unit and Ottawa Public Health (including urban, rural, and Indigenous communities such as Akwesasne).\n\nPrimary Care Providers:\n\n* Must be a licensed Family Physician (FP) or Nurse Practitioner (NP) in a practice of at least 2 PCPS.\n* The providers must be offering comprehensive primary care to a panel of patients (not solely urgent care or walk-in services).\n* Must work in a computerized primary care clinic with an electronic medical record system.\n* Must expect to remain in practice for at least 24 months.\n* Must be located in Eastern Ontario.\n* Must be willing to use the Canadian Primary Care Information Network (CPIN) to deliver Heat Smart messages and surveys.\n* Must be using Cliniconex or Qualtrics as a practice tool for communication enabling outreach before the patients are invited to consent to participate in the study.\n\nExclusion Criteria:\n\nPatients who do not read French or English will be excluded from the study as they will not be able to give informed consent or to fill out the surveys. Patients who do not have an email address or text messaging service will be excluded for the same reason. Minors, patients with dementia and people who cannot read and write in English or French will not be eligible because the automated approach to surveying patients makes it impractical to properly obtain their consent.",{"count":100,"type":23},20000,[26],"Extreme heat events pose a significant health threat in Canada, as demonstrated by the 2021 heat wave that claimed over 600 lives in Western Canada. Most heat-related deaths occur indoors and are preventable. Primary care providers (PCPs), who serve 88% of Canadians, are uniquely positioned to identify and support at-risk individuals. Heat Smart, in alignment with Heat Alert and Response Systems (HARS), aims to bridge the gap between primary care and public health to enhance community resilience and reduce health inequities related to extreme heat events.\n\nThis randomized control trial in Eastern Ontario will examine whether patients receiving tailored digital health messages from their family physician or nurse practitioner change their behaviour to protect themselves from extreme heat-related illness. The Heat Smart study will:\n\n* Assess risk: Analyze electronic medical records and patient surveys to identify vulnerable individuals.\n* Deliver tailored messages: Send personalized digital guidance via e-mail or text, offering heat safety advice and local resource information in English and French.\n* Issue early warning alerts: Notify at-risk patients of upcoming heat events, prompting action.\n* Evaluate impact: Use surveys and health data to measure effectiveness in reducing heat-related health impacts.\n\nShort-term outcomes include increased awareness and preparedness among patients about heat-related health risks. Long-term goals involve scaling the intervention across Canada to reduce heat-related illnesses, enhance social connectedness, and decrease healthcare utilization.",[104,105,106,107,108,109,29,110,111],"Heathly Subjects","Primary Health Care","Climate Change","Public Health","Preventive Health Services (PREV HEALTH SERV)","Environmental Exposure","Heat Stress Disorders","Heat Exposure",[113,114,115,116,117,118],"primary care","digital messaging","heatwave","climate change","public health","CPIN","2025-06-09",{"date":121,"type":45},"2025-06-17",{"date":123,"type":45},"2025-04-01",{"date":125,"type":23},"2028-03-31",{"name":127,"class":52},"Hopital Montfort",{"id":129,"slug":130,"hasResults":11,"nctId":131,"briefTitle":132,"officialTitle":133,"acronym":134,"eligibilityCriteria":135,"healthyVolunteers":17,"sex":18,"minAge":136,"maxAge":137,"enrollmentInfo":138,"targetDuration":4,"studyType":24,"phases":140,"briefSummary":141,"conditions":142,"keywords":147,"overallStatus":151,"whyStopped":4,"lastUpdateSubmitDate":152,"lastUpdatePostDateStruct":153,"startDateStruct":155,"completionDateStruct":157,"leadSponsor":159,"locationsCount":4},"100574072","options-for-navigating-talking-about-risk-and-adolescent-choices-100574072","NCT06754527","Options for Navigating Talking About Risk and Adolescent Choices","Emotion Regulation Intervention to Prevent Substance Use Among Youth in the Child Welfare System","ON-TRAC","Inclusion Criteria:\n\n* Contact with the Rhode Island child welfare system\n* Caregiver who is a parent\u002Fguardian of a child who experienced maltreatment\n* Caregiver who speaks English or Spanish\n* Caregiver who does not have developmental delays\n* Adolescent who is between 12-15 years of age\n* Adolescent who is fluent in English\n* Adolescent who has active follow-up with the Rhode Island child welfare system due to an indicated finding of abuse or neglect in the past year\n\nExclusion Criteria:\n\n* Adolescent who cannot read at a 4th grade level\n* Adolescent who has a sibling who has participated in the program\n* Adolescent who has developmental delays\n* Adolescent who lacks parental consent for the study","12 Years","15 Years",{"count":139,"type":23},200,[26],"This study will examine the effectiveness of ON-TRAC (Options for Navigating Talking about Risk and Adolescent Choices), which is an online substance use prevention program that also teaches emotion regulation skills. 200 adolescents, 12-15 years of age, will be randomized to ON-TRAC or a wait list comparison group (who will be offered the intervention at the end of their study participation) to determine impact on substance use, emotion regulation abilities, mental health symptoms, and other risk behavior outcomes.",[143,144,145,146,29,78],"Substance Use (Drugs, Alcohol)","Substance Use Risk","Substance Use","Emotion Regulation",[148,149,150],"adolescent substance use","emotion regulation","risk reduction","NOT_YET_RECRUITING","2024-12-30",{"date":154,"type":45},"2025-01-01",{"date":156,"type":23},"2026-03-01",{"date":158,"type":23},"2029-02-01",{"name":160,"class":52},"Rhode Island Hospital",{"id":162,"slug":163,"hasResults":11,"nctId":164,"briefTitle":165,"officialTitle":165,"acronym":4,"eligibilityCriteria":166,"healthyVolunteers":17,"sex":167,"minAge":4,"maxAge":4,"enrollmentInfo":168,"targetDuration":4,"studyType":24,"phases":170,"briefSummary":171,"conditions":172,"keywords":4,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":179,"lastUpdatePostDateStruct":180,"startDateStruct":182,"completionDateStruct":184,"leadSponsor":186,"locationsCount":53},"100506168","generation-r-next---optimaal-opgroeien-100506168","NCT05870878","Generation R Next - Optimaal Opgroeien","Inclusion Criteria:\n\nWomen and their parents:\n\n* Planning a pregnancy or early pregnancy up to \\\u003C 12 weeks\n* With the presence of at least one of the predetermined risk factors\n* Residential address in the municipality of Rotterdam and expected residential address in the municipality of Rotterdam at the birth of their child\n* Consent for participation\n\nExclusion Criteria:\n\nWomen and their partners:\n\n* Temporary or complete withdrawal from participation\n* Gestational age \\> 12+0 at study entry","FEMALE",{"count":169,"type":23},1750,[26],"The aim of this randomized controlled trial is to improve birth outcomes and long-term outcomes in mother and child by optimizing lifestyle,nutrition and stress experience in the preconception period and early pregnancy in women and men\n\nThe main research question that will be addressed is: Does an intervention focused on optimizing preconception and early pregnancy lifestyle, nutrition and stress improve the birth outcomes and long-term outcomes in mother and child?\n\nParticipants will receive an individual lifestyle consultation at the start of the study. Depending on their study arm, participants will receive an additional lifestyle program focused on health during preconception and early pregnancy, coping with stress and adherence to a healthy(er) lifestyle. The given advices are based on national guidelines.\n\nResearchers will compare the intervention group and control group to see if (adherence to) this lifestyle program improve birth outcomes and long-term outcomes in mother and child.",[173,174,175,176,177,178,29],"Pregnancy Early","Outcome, Adverse Birth","Lifestyle Factors","Preconception Care","Pregnancy Outcome","Pregnancy Complications","2024-08-30",{"date":181,"type":45},"2024-09-04",{"date":183,"type":45},"2023-01-19",{"date":185,"type":23},"2030-11-08",{"name":187,"class":52},"Erasmus Medical Center",{"id":189,"slug":190,"hasResults":11,"nctId":191,"briefTitle":192,"officialTitle":193,"acronym":194,"eligibilityCriteria":195,"healthyVolunteers":11,"sex":18,"minAge":196,"maxAge":197,"enrollmentInfo":198,"targetDuration":4,"studyType":200,"phases":4,"briefSummary":201,"conditions":202,"keywords":204,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":206,"lastUpdatePostDateStruct":207,"startDateStruct":209,"completionDateStruct":211,"leadSponsor":213,"locationsCount":53},"100495554","long-term-cardiovascular-disease-event-risk-for-patients-undergoing-major-non-cardiac-surgery-100495554","NCT05732714","Long Term Cardiovascular Disease Event Risk for Patients Undergoing Major Non-Cardiac Surgery","Long Term Cardiovascular Disease Event Risk for Patients Undergoing Major Non-Cardiac","CVD-10y-postop","Inclusion Criteria:\n\n* Age 45 - 75 years\n* Scheduled for intermediate- to high risk non-cardiac surgery (intra-thoracic or intra-abdominal surgery, all vascular surgery, intra-cranial neurosurgery, spine surgery)\n* Expected post-operative length of stay of at least two days, according to the surgeon's expectation\n* At least two of the following CVD risk factors:\n\nHistory of: Hypertension, Diabetes, Coronary artery disease, Chronic heart failure, Chronic kidney disease, Cerebrovascular disease, Peripheral vascular disease.\n\nObesity (BMI \\>25 kg\u002Fm2), Current smoking, Poor exercise capacity (\\\u003C4 METS)\n\nExclusion Criteria:\n\n* Currently participating in a CVD risk reduction program\n* Patient is scheduled to undergo transplant or has undergone emergency surgery\n* Life expectancy \\\u003C1 year (palliative surgery)\n* Recent (\\\u003C6 months) myocardial infarction or stroke\n* Surgery scheduled \\\u003C1 month\n* Inability to effectively communicate","45 Years","75 Years",{"count":199,"type":23},50,"OBSERVATIONAL","The goal of this observational study is to learn whether the healthy lifestyle choices made around surgery can influence an individual's long term risk of developing cardiovascular disease. Patients will be observed 1-month prior to and 3-months following surgery to assess their risk of developing cardiovascular disease.",[203,29],"Cardiovascular Diseases",[205],"Intermediate to high risk non-cardiac surgery","2024-08-12",{"date":208,"type":45},"2024-08-13",{"date":210,"type":23},"2024-08",{"date":212,"type":23},"2025-10",{"name":214,"class":52},"University Health Network, Toronto"]