[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"health-knowledge-attitudes-practice\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:health-knowledge-attitudes-practice":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,20,0,[8,45,73,115,145,169,206,230,260,284,306,336,370,397,418,449,470,494,525,548],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100543491","adapting-enhanced-recovery-programs-for-low-health-literacy-patients-100543491",false,"NCT06356558","Adapting Enhanced Recovery Programs for Low Health Literacy Patients","Inclusion Criteria:\n\n* Adult patients \\>= 18 years of age undergoing surgery under an enhanced recovery program (ERPs)\n* Adult caregivers\u002Fproviders, organizational leaders, \\>= 18 years of age with direct or indirect involvement with ERP implementation\n* All genders\n* All race\u002Fethnicities\n* Able to consent\n* English-speaking\n\nExclusion Criteria:\n\n* Child (\\\u003C18 years of age)\n* Patients undergoing operations not included under ERPs\n* Participants unable to consent for the study\n* Participants whose mental state excludes them from being able to understand contents of the informed consent form and\u002For patients whose family members or patient representative do not wish for them to participate in the study",true,"ALL","18 Years",{"count":19,"type":20},1050,"ESTIMATED","INTERVENTIONAL",[23],"NA","Low health literacy patients are a vulnerable population at high-risk for surgical disparities including longer hospital stays, more complications, and more readmissions. This study will adapt enhanced recovery programs (ERPs) to low health literacy patients with a multilevel, health literacy-based implementation strategy (called VISACT - VISuAl aids, Coach providers in communication, and Train organizations in health literacy) to improve ERP fidelity and thereby outcomes. In the final aim of this project (Specific Aim 3), the VISACT intervention will be tested in a pilot trial. Findings from this study will lay the foundation for a multi-institutional stepped-wedge trial and establish key principles for adapting interventions to eliminate disparities.",[26,27,28],"Surgery","Health Knowledge, Attitudes, Practice","Colorectal Disorders",[26,30,31],"Health Literacy","Enhanced Recovery","RECRUITING","2026-06-25",{"date":35,"type":36},"2026-06-29","ACTUAL",{"date":38,"type":36},"2026-06-15",{"date":40,"type":20},"2028-05-01",{"name":42,"class":43},"University of Alabama at Birmingham","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":15,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":21,"phases":55,"briefSummary":56,"conditions":57,"keywords":62,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":72},"100509058","african-americans-aa-communities-speak-100509058","NCT05908487","African Americans (AA) Communities Speak","African Americans (AA) Communities Speak: Partnering With AA in the North and South to Train Palliative Care Clinicians to Address Interpersonal and Systemic Racism and Provide Culturally Aligned Care.","AACS","Inclusion Criteria: Aim 1.1\n\nPerson with serious Illness:\n\n* Self-identified as African American (i.e., born, raised, and lived primarily in the US)\n* Non-Hispanic or Latino\n* Age ≥60 years\n* English-speaking\n* Has been diagnosed with a condition that fits into one of 3 illness paradigms including cancer, cardiac disease, pulmonary disease, neuro-degenerative disease, renal disease, stroke, sepsis, hepatic disease)\n* Callahan Six-Item Screener score ≥4\n* Able to complete baseline surveys.\n\nBereaved family member:\n\n* Self-identified as African American (i.e., born, raised, and lived primarily in the US)\n* Non-Hispanic or Latino\n* Age ≥60 years\n* English-speaking\n* Loved one dies in the last 12 months and was diagnosed with a condition that fits into one of 3 illness paradigms including cancer, cardiac disease, pulmonary disease, neuro- degenerative disease, renal disease, stroke, sepsis, hepatic disease)\n* Callahan Six-Item Screener score ≥4\n* Able to complete baseline surveys.\n\nExclusion Criteria\n\nPerson with serious illness:\n\n-Cannot be receiving hospice care\n\nBereaved Family Member:\n\n-Cannot be a paid \"sitter\"\n\nInclusion Criteria: Aim 1.2\n\nBereaved Family member:\n\n* Self-identified as African American (i.e., born, raised, and lived primarily in the US)\n* Non-Hispanic or Latino\n* Age ≥60 years\n* English-speaking\n* Loved one dies in the last 12 months and was diagnosed with a condition that fits into one of 3 illness paradigms including cancer, cardiac disease, pulmonary disease, neuro- degenerative disease, renal disease, stroke, sepsis, hepatic disease)\n* Callahan Six-Item Screener score ≥4\n* Able to complete baseline surveys\n\nPastors:\n\n* Self-identifying as African American\n* White, Non-Hispanic or Latino\n* Sged ≥18 years old.\n\nInclusion Criteria: Aim 3\n\nClinician eligibility:\n\n* Practice at a University of Alabama at Birmingham (UAB) or Montefiore\u002FEinstein site that provides care to patients eligible for outcomes surveys\n* At least 3 months of clinical practice at the study site prior to the intervention training to measure pre-intervention patient surveys\n\nExclusion criteria:\n\n-Lack of at least 3 months of clinical practice at the study site prior to the intervention training.\n\nPatient eligibility:\n\n* Self-identified as African American (i.e., born, raised, and lived primarily in the US)\n* Non-Hispanic or Latino, 3. age ≥60 years\n* English-speaking\n* Has been diagnosed with a condition that fits into one of 3 illness paradigms including cancer, cardiac disease, pulmonary disease, neuro-degenerative disease, renal disease, stroke, sepsis, hepatic disease)\n* Callahan Six-Item Screener score ≥4\n* Able to complete baseline surveys.\n\nExclusion criteria include:\n\n-Currently receiving hospice care.\n\nFamily member eligibility:\n\n* Age ≥ 18 years\n* English-speaking\n* Community-dwelling\n* Unpaid care provider of a person with a serious illness.\n\nExclusion criteria: 1. Cannot be a paid \"sitter\".",{"count":54,"type":20},60,[23],"African Americans are less likely to receive quality end-of-life (EoL) care. Addressing disparities in EoL care will need efforts to support a better understanding of African American patients' EoL cultural values and preferences for EoL communication and the impact of historical and ongoing care delivery inequities in healthcare settings.\n\nOur proposed \"Caring for Older African Americans\" training program is designed to empower clinicians to improve goal-concordant EoL care delivery by using community-developed storytelling videos to create empathy with experiences of racism in EoL care, guidelines for culturally concordant EoL care delivery, and an implicit bias recognition and management training to mitigate bias in goals of care communication.",[58,27,59,60,61],"Healthy Aging","Social Responsibility","Care Eliciting Behavior","Racism, Systemic",[63],"goal concordant care older African American CBPR end-of-life","2026-05-05",{"date":66,"type":36},"2026-05-07",{"date":68,"type":36},"2025-02-27",{"date":70,"type":20},"2028-07",{"name":42,"class":43},2,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":79,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":81,"minAge":17,"maxAge":4,"enrollmentInfo":82,"targetDuration":4,"studyType":21,"phases":84,"briefSummary":85,"conditions":86,"keywords":90,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":109,"completionDateStruct":111,"leadSponsor":113,"locationsCount":4},"100635234","womenfocused-education-in-cardiac-rehabilitation-wecare-pilot-rct-100635234","NCT07550036","WomenFocused Education in CArdiac REhabilitation (WECARE) Pilot RCT","Women Education in CArdiac REhabilitation (WE CARE): a Pilot Randomized Controlled Trial for Effectiveness, Implementation, Utilization, and Acceptability of Cardiac College for Women Across Canada","WE-CARE","Inclusion Criteria:\n\n* Identify as a woman\n* Aged 18 years or older\n* Enrolled in a participating cardiac rehabilitation program\n* Diagnosis consistent with cardiac rehabilitation eligibility (e.g., coronary artery disease, myocardial infarction, revascularization procedures, spontaneous coronary artery dissection, myocardial infarction with non-obstructive coronary arteries, Takotsubo cardiomyopathy, or heart failure)\n* Able to provide informed consent\n* Able to participate in educational sessions in English or French (site-dependent)\n\nExclusion Criteria:\n\n* Medical, cognitive, or psychiatric conditions that would prevent participation in educational sessions or completion of study questionnaires\n* Inability to access or use online educational sessions or digital materials required for the intervention","FEMALE",{"count":83,"type":20},50,[23],"The goal of this pilot clinical trial is to learn if a women-focused education program can improve knowledge, health, and well-being in women with heart disease who are attending cardiac rehabilitation. It will also help researchers understand if this program can be delivered successfully in different rehabilitation programs.\n\nThe main questions it aims to answer are:\n\n* Is it feasible to deliver this women-focused education program within routine cardiac rehabilitation programs?\n* Do women who receive this program show improvements in heart health knowledge, quality of life, and healthy behaviours?\n\nResearchers will compare women who receive the Cardiac College for Women program plus usual cardiac rehabilitation to those who receive usual cardiac rehabilitation alone to see if the program leads to better outcomes.\n\nParticipants will:\n\n* Be randomly assigned to receive either the women-focused education program or usual care\n* Attend cardiac rehabilitation as part of their regular care\n* Complete questionnaires at the start and end of the program\n* (If in the intervention group) attend online education sessions and use supporting materials\n* (Optional) take part in a group discussion about their experience after completing the program",[87,88,27,89],"Cardiovascular Diseases","Heart Diseases","Behavior, Health",[91,92,93,94,95,96,97,98,99,100,101,102,103,104],"Cardiac Rehabilitation","Women's Health","Patient Education","Cardiovascular Disease Prevention","Secondary Prevention","Health Education","Women-Focused Care","Gender-Specific Care","Digital Health \u002F Virtual Care","Self-Management","Health Behaviour Change","Quality of Life","Feasibility Study","Pilot Randomized Controlled Trial","NOT_YET_RECRUITING","2026-04-17",{"date":108,"type":36},"2026-04-24",{"date":110,"type":20},"2026-09-01",{"date":112,"type":20},"2027-09-01",{"name":114,"class":43},"University Health Network, Toronto",{"id":116,"slug":117,"hasResults":11,"nctId":118,"briefTitle":119,"officialTitle":120,"acronym":121,"eligibilityCriteria":122,"healthyVolunteers":11,"sex":81,"minAge":17,"maxAge":123,"enrollmentInfo":124,"targetDuration":4,"studyType":21,"phases":126,"briefSummary":127,"conditions":128,"keywords":132,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":135,"lastUpdatePostDateStruct":136,"startDateStruct":138,"completionDateStruct":140,"leadSponsor":142,"locationsCount":144},"100459897","mhealth-india-postnatal-health-intervention-effectiveness-100459897","NCT05268588","mHealth India Postnatal Health Intervention Effectiveness","Effectiveness of an mHealth Interactive Education and Social Support Intervention for Improving Postnatal Health","Kushal Maa","Inclusion Criteria:\n\n* Pregnant (28-32 weeks gestational age)\n* Speak local language\n* Personal mobile phone or willing to accept study phone\n* Able to provide informed consent\n\nExclusion Criteria:\n\n* Do not speak local language\n* No personal phone or unwilling to accept study phone\n* Unable to provide informed consent","49 Years",{"count":125,"type":20},2100,[23],"The goal of this study is to assess the effectiveness of a culturally-tailored mobile interactive education and support group intervention to supplement standard postpartum care activities in comparison to standard care alone on health-related behaviors and health outcomes in a randomized controlled trial among 2100 postpartum Indian women living in 3 geographically diverse Indian states to estimate the impact on maternal and neonatal health-related knowledge, health-related behaviors, and health outcomes. The investigators also seek to characterize mechanisms of impact including knowledge, social support, self-efficacy, and behavior change, and determine the cost-effectiveness.",[27,129,130,131],"Post Partum Depression","Breastfeeding","Nutrition, Healthy",[133,134],"mHealth","group care","2026-03-31",{"date":137,"type":36},"2026-04-01",{"date":139,"type":36},"2025-01-20",{"date":141,"type":20},"2027-05-31",{"name":143,"class":43},"University of California, San Francisco",3,{"id":146,"slug":147,"hasResults":11,"nctId":148,"briefTitle":149,"officialTitle":149,"acronym":4,"eligibilityCriteria":150,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":151,"targetDuration":4,"studyType":21,"phases":153,"briefSummary":154,"conditions":155,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":160,"lastUpdatePostDateStruct":161,"startDateStruct":163,"completionDateStruct":165,"leadSponsor":167,"locationsCount":72},"100612078","the-effect-of-a-transtheoretical-model-based-educational-intervention-on-first-year-nursing-students-hpv-knowledge-health-beliefs-and-vaccination-behavior-intentions-100612078","NCT07248904","The Effect of a Transtheoretical Model-Based Educational Intervention on First-Year Nursing Students' HPV Knowledge, Health Beliefs, and Vaccination Behavior Intentions","Inclusion Criteria:\n\n* First-year students enrolled in the Nursing Department of the Faculty of Health Sciences\n* Provide written informed consent to participate\n* Agree to attend all educational sessions and data collection appointments during the study period\n* Have sufficient Turkish literacy to read and understand study materials\n* Have not previously received any comprehensive education about HPV infection or HPV vaccination\n\nExclusion Criteria:\n\n* Students who do not agree to participate in the study\n* Students who do not provide written informed consent",{"count":152,"type":20},88,[23],"The purpose of this study is to examine the impact of a structured educational program based on the Transtheoretical Model (TTM) on HPV knowledge, health beliefs, and vaccination behavioral intentions among first-year nursing students. The study will also evaluate how the intervention affects students' HPV vaccine readiness compared to the TTM.\n\nThe primary questions addressed by the study are:\n\n* Does the TTM-based educational intervention increase students' knowledge about HPV and the HPV vaccine?\n* Does the program change students' health beliefs regarding susceptibility, severity, benefits, and barriers to HPV and the HPV vaccine?\n* Does the program improve students' intentions and readiness to receive the HPV vaccine?\n* Do students move to a higher behavioral readiness stage (from Precontemplation to Contemplation, Preparation, Action, or Maintenance) after the intervention?\n\nThe researcher will compare the TTM-based educational intervention with a control group that did not receive structured education to determine whether a personalized, stage-based approach is more effective in improving HPV-related outcomes among nursing students.\n\nParticipants will:\n\n* Complete baseline questionnaires measuring HPV knowledge, health beliefs, and vaccination intention.\n* The experimental group (intervention group) will receive personalized TTM-based education, face-to-face instruction in modules aligned with the five TTM phases (Precontemplation, Contemplation, Preparation, Action, and Maintenance).\n* The experimental group will participate in educational sessions designed to raise awareness, correct misinformation, support decision-making, and encourage protective behaviors.\n* The control group will not receive any educational program.\n* All participants in the experimental and control groups will complete the same questionnaires again to assess changes after the intervention.\n\nThe TTM-based educational intervention provides:\n\n* Staged counseling\n* Information about HPV and the HPV vaccine\n* Activities to raise awareness, strengthen motivation, and support vaccination adoption\n* Personalized feedback based on student readiness\n* Structured modules focusing on knowledge, belief, and behavior change strategies\n\nThe study population included first-year nursing students enrolled in the Faculty of Health Sciences. A total of 88 participants will be recruited and randomly assigned to either the intervention (n=44) or control (n=44) groups through simple randomization.\n\nThe results of this study are expected to contribute to the development of evidence-based education strategies in nursing, support of behavioral change models in health education, and strengthen the role of future nurses in HPV prevention, vaccine advocacy, and public health practice.",[156,157,27,158,159],"Human Papillomavirus (HPV)","Papillomavirus Vaccines","Students, Nursing","Health Behavior","2026-03-26",{"date":162,"type":36},"2026-03-27",{"date":164,"type":36},"2026-01-16",{"date":166,"type":20},"2026-04-30",{"name":168,"class":43},"Cukurova University",{"id":170,"slug":171,"hasResults":11,"nctId":172,"briefTitle":173,"officialTitle":173,"acronym":174,"eligibilityCriteria":175,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":176,"targetDuration":4,"studyType":178,"phases":4,"briefSummary":179,"conditions":180,"keywords":191,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":197,"lastUpdatePostDateStruct":198,"startDateStruct":200,"completionDateStruct":202,"leadSponsor":204,"locationsCount":72},"100331231","cuhk-brain-health-longitudinal-study-100331231","NCT03592563","CUHK Brain Health Longitudinal Study","BHS","Inclusion Criteria:\n\n1. Adult ≥ 18 years of age\n2. Fulfilling criteria for membership in one of these three groups:\n\n   * Red group: established diagnosis of one or more neurological and\u002For psychiatric conditions\n   * Yellow group: high-risk to develop one or more neurological and\u002For psychiatric conditions\n\n     1. family history (first degree relative) one or more neurological and\u002For psychiatric conditions\n     2. examination, imaging or laboratory findings consistent with pre-symptomatic stages of one or more neurological and\u002For psychiatric disorders\n   * Green group: not meeting criteria for Red or Yellow groups, but interested in longitudinal research on maintenance and\u002For improvement of brain health\n3. Subject provides informed consent by signing and dating the written informed consent form\n4. Subject is willing to answer health questionnaires and be followed longitudinally\n\nExclusion Criteria:\n\n* None",{"count":177,"type":20},5000,"OBSERVATIONAL","The goal of this study is to develop a large longitudinal cohort of individuals diagnosed with or at high risk for brain diseases (both neurological and psychiatric in nature), in order to identify risk factors that contribute to neurological and psychiatric diseases over time. The investigators seek to capture relevant information from medical records, electronically administered questionnaires and follow up phone-based interviews. The investigators expect to eventually have sufficient power from our dataset to examine risk factors for a variety of brain disorders, both individually and in aggregate. Our ultimate goal is to offer scientifically validated ways to preserve and promote brain health by working with our patients' needs and tracking their progress over time.",[181,182,183,184,185,186,187,188,189,27,190,58],"Stroke, Ischemic","Stroke Syndrome","Stroke","Stroke, Acute","Dementia","Brain Ischemia","Brain Diseases","Alzheimer Disease","Health Attitude","Health Personnel Attitude",[192,193,194,195,196],"stroke","dementia","Alzheimer disease","Health Brain","Health knowledge","2026-02-21",{"date":199,"type":36},"2026-02-24",{"date":201,"type":36},"2019-07-01",{"date":203,"type":20},"2048-12-31",{"name":205,"class":43},"Chinese University of Hong Kong",{"id":207,"slug":208,"hasResults":11,"nctId":209,"briefTitle":210,"officialTitle":211,"acronym":4,"eligibilityCriteria":212,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":213,"targetDuration":4,"studyType":21,"phases":214,"briefSummary":215,"conditions":216,"keywords":221,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":222,"lastUpdatePostDateStruct":223,"startDateStruct":225,"completionDateStruct":227,"leadSponsor":228,"locationsCount":44},"100624532","virtual-reality-enhanced-parent-education-in-neonatal-intensive-care-100624532","NCT07410858","Virtual Reality-Enhanced Parent Education in Neonatal Intensive Care","Virtual Reality-Enhanced Parent Education and Its Effect on Neonatal Intensive Care Practices: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Parent or legal guardian of a neonate admitted to the Neonatal Intensive Care Unit (NICU) within 72 hours of admission\n* Age 18 years or older\n* Able to read and understand the study language (Arabic)\n* Willing to provide informed consent and participate in study procedures\n\nExclusion Criteria:\n\n* Parent with a confirmed diagnosis of epilepsy, vestibular disorder, or any medical condition that contraindicates virtual reality exposure\n* Parent of a neonate expected to be discharged or transferred within 48 hours\n* Parent unable to complete study procedures or assessments",{"count":54,"type":20},[23],"This randomized pilot clinical trial aims to evaluate the effectiveness and feasibility of virtual reality (VR)-enhanced parent education in improving neonatal intensive care unit (NICU) caregiving practices among parents of hospitalized neonates. The study will also examine the safety and tolerability of VR use among parents.\n\nResearchers will compare VR-enhanced education with standard NICU parent education to determine whether immersive VR training improves parents' knowledge, confidence, and ability to perform caregiving tasks.\n\nParticipants will be randomly assigned to receive either VR-enhanced education or standard education. Participants receiving VR education will engage in short immersive sessions demonstrating NICU orientation and caregiving procedures. All participants will complete assessments and observations related to caregiving practices and VR tolerability throughout the study period.",[217,218,219,220,27],"Neonatal Intensive Care Units","Premature Infant","Parent Education","Virtual Reality",[220,217,219,218],"2026-02-13",{"date":224,"type":36},"2026-02-18",{"date":226,"type":36},"2026-01-01",{"date":166,"type":20},{"name":229,"class":43},"Jouf University",{"id":231,"slug":232,"hasResults":11,"nctId":233,"briefTitle":234,"officialTitle":235,"acronym":4,"eligibilityCriteria":236,"healthyVolunteers":15,"sex":16,"minAge":237,"maxAge":238,"enrollmentInfo":239,"targetDuration":4,"studyType":178,"phases":4,"briefSummary":241,"conditions":242,"keywords":243,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":164,"lastUpdatePostDateStruct":252,"startDateStruct":254,"completionDateStruct":256,"leadSponsor":258,"locationsCount":72},"100230850","pcori-cer-1306-03385-lung-cancer-screening-decision-aid-development-and-testing-100230850","NCT02282969","PCORI-CER-1306-03385 Lung Cancer Screening Decision Aid Development and Testing","Promoting Informed Decisions About Lung Cancer Screening: Decision Aid Update and Measures Development","Inclusion Criteria:\n\n1. Men and women 55 to 80 years of age.\n2. Participants must speak English.\n3. Current smoker or quit smoking within the past 15 years.\n\nExclusion Criteria:\n\n1\\. History of lung cancer.","55 Years","80 Years",{"count":240,"type":20},620,"Objectives:\n\nThis protocol addresses the first phase of a larger project funded by the Patient-Centered Outcomes Research Institute to help heavy smokers make informed decisions about lung cancer screening with low-dose computed tomography (CT). A separate IRB protocol will be submitted for the larger, comparative study. In this initial development phase, our prototype patient decision aid will be updated to reflect current guidelines about lung cancer screening. The updated aid will then be pilot-tested in a new sample of patients. In addition, several of the study measures will be refined and further developed in preparation for the larger study.\n\nThe specific aims of the measures and decision aid development phase of this project are as follows:\n\nUpdate the aid to reflect current screening guidelines and refine the aid via cognitive testing with patients\u002Fsmokers; and pilot test the updated aid for acceptability with patients\u002Fsmokers.\n\nModify our current measure of lung cancer knowledge, conduct cognitive testing of the new measure with patients\u002Fsmokers, and evaluate the reliability of the new measure in a sample patients\u002Fsmokers.",[27],[244,245,246,247,248,249,250,251],"Cancer Prevention","Smokers","Quit smoking","Interviews","Questionnaires","Surveys","Lung cancer screening","Patient decision aid",{"date":253,"type":36},"2026-01-20",{"date":255,"type":36},"2014-07-11",{"date":257,"type":20},"2028-08-31",{"name":259,"class":43},"M.D. Anderson Cancer Center",{"id":261,"slug":262,"hasResults":11,"nctId":263,"briefTitle":264,"officialTitle":265,"acronym":4,"eligibilityCriteria":266,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":267,"enrollmentInfo":268,"targetDuration":4,"studyType":21,"phases":269,"briefSummary":270,"conditions":271,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":276,"lastUpdatePostDateStruct":277,"startDateStruct":278,"completionDateStruct":280,"leadSponsor":282,"locationsCount":44},"100585101","feasibility-of-a-nutrition-intervention-for-patients-with-prediabetes-at-a-federally-qualified-health-center-100585101","NCT06897982","Feasibility of a Nutrition Intervention for Patients With Prediabetes at a Federally Qualified Health Center","One-arm Feasibility and Acceptability Pilot Study of a Community-informed Nutrition Intervention to Recruit, Engage, and Retain Patients Who Are Eligible to Participate in the Diabetes Prevention Program at Two Community Health Centers in Los Angeles","Inclusion Criteria:\n\n* 18+ years old\n* BMI of 25 or higher (23 or higher if Asian)\n* Meet specific blood sugar test criteria indicating prediabetes, such as a fasting plasma glucose level between 110-125 mg\u002FdL or an A1C level between 5.7-6.4%\n* Not be diagnosed with type 1 or type 2 diabetes\n* Moderate to high risk of having prediabetes or a known diagnosis of prediabetes by their medical provider in the last 12 months.\n* Eligible or enrolled in the Diabetes Prevention Program\n\nExclusion Criteria:\n\n* Younger than 18 years of age\n* BMI of less than 25 or higher (or under 23 if Asian)\n* Does not meet specific blood sugar test criteria indicating prediabetes, such as a fasting plasma glucose level between 110-125 mg\u002FdL or an A1C level between 5.7-6.4%\n* Currently diagnosed with type 1 or type 2 diabetes\n* Has not been diagnosed as moderate to high risk of having prediabetes or having a known diagnosis of prediabetes by their medical provider in the last 12 months.","99 Years",{"count":5,"type":20},[23],"The purpose of the study is to assess the feasibility and acceptability of incorporating hands-on nutritional demonstrations to enhance the Diabetes Prevention Program (DPP) curriculum among patients who are at-risk for prediabetes",[272,273,27,131,274,275],"Prediabetic State","PreDiabetes","Acceptability of Health Care","Obesity Prevention","2026-01-15",{"date":253,"type":36},{"date":279,"type":36},"2025-12-08",{"date":281,"type":20},"2027-02-28",{"name":283,"class":43},"Cedars-Sinai Medical Center",{"id":285,"slug":286,"hasResults":11,"nctId":287,"briefTitle":288,"officialTitle":289,"acronym":4,"eligibilityCriteria":290,"healthyVolunteers":11,"sex":81,"minAge":17,"maxAge":4,"enrollmentInfo":291,"targetDuration":4,"studyType":178,"phases":4,"briefSummary":293,"conditions":294,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":297,"lastUpdatePostDateStruct":298,"startDateStruct":300,"completionDateStruct":302,"leadSponsor":304,"locationsCount":44},"100598135","breastfeeding-myths-and-mothers-motivation-100598135","NCT07067554","Breastfeeding Myths and Mothers' Motivation","An Investigation of the Relationship Between Mothers' Susceptibility to Breastfeeding Myths and Their Motivation to Breastfeed","Inclusion Criteria:\n\n* Having an infant aged 0-6 months\n* Having breastfed the baby at least once\n* Voluntarily agreeing to participate in the study\n\nExclusion Criteria:\n\n* Having a physical or psychiatric health condition that prevents breastfeeding\n* Having had a multiple (twin or more) pregnancy\n* Exclusively formula-feeding the baby",{"count":292,"type":20},191,"Breast milk is a unique and irreplaceable source of nutrition for infants, offering protection against many common childhood diseases due to its natural sterility, accessibility, and immune-boosting antibodies. Exclusive breastfeeding for the first six months of life is critical for healthy growth, development, and immune support. Despite global recommendations by WHO and UNICEF, lack of knowledge and inadequate support continue to hinder optimal breastfeeding practices.\n\nOne major barrier is the persistence of cultural myths and misconceptions, such as \"colostrum should be discarded,\" or \"infants need water after every feeding.\" These unfounded beliefs may reduce mothers' confidence and lead to early cessation of breastfeeding or premature introduction of complementary foods.\n\nThis study aims to examine the relationship between mothers' belief in breastfeeding myths and their motivation to breastfeed. While prior research has explored each factor individually, no known studies have analyzed their interaction.",[130,295,27,296],"Maternal Behavior","Motivation","2025-09-25",{"date":299,"type":36},"2025-09-30",{"date":301,"type":36},"2025-09-09",{"date":303,"type":20},"2026-07-30",{"name":305,"class":43},"Acibadem University",{"id":307,"slug":308,"hasResults":11,"nctId":309,"briefTitle":310,"officialTitle":310,"acronym":4,"eligibilityCriteria":311,"healthyVolunteers":15,"sex":312,"minAge":313,"maxAge":314,"enrollmentInfo":315,"targetDuration":4,"studyType":21,"phases":317,"briefSummary":319,"conditions":320,"keywords":321,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":328,"lastUpdatePostDateStruct":329,"startDateStruct":331,"completionDateStruct":333,"leadSponsor":334,"locationsCount":44},"100563675","phase-4-effect-of-endurance-training-induced-coenzyme-q10-coq10-supplementation-on-myokine-exerkine-secretion-and-cognitive-functions-in-long-distance-runners-100563675","NCT06619249","Effect of Endurance Training-Induced Coenzyme Q10 (CoQ10) Supplementation on Myokine, Exerkine Secretion and Cognitive Functions in Long-Distance Runners","Inclusion Criteria:\n\n* training experienced for minimum 2 years\n* running training at least 2 times per week\n* Personal Best on 10k (\\\u003C50 minutes)\n\nExclusion Criteria:\n\n* taking supplements which can interrupt primary outcomes (vitamin D, omega-3 fatty acids)\n* injured in last 6 months to avoid n number reduction","MALE","30 Years","50 Years",{"count":316,"type":20},24,[318],"PHASE4","The goal of this clinical trial is to learn if CoQ10 amplifies endurance training-induced myokine and exerkine secretion and if those changes influences cognition in long-distance runners.\n\nDoes 4-week high-dosage CoQ10 supplementation increase the secretion of myokine, exerkine sercetion? Does the above-mentioned intervention improve the cognitive function in long distance runners?\n\nParticipants will:\n\nTake CoQ10 or a placebo every day for 4 weeks. Visit the laboratory once every 4 weeks for checkups and tests. Keep the participants' food and training diary.",[27],[322,323,324,325,326,327],"Coenzyme Q10","Supplementation","Myokine","Exerkine","Cognition","Long-distance runners","2025-08-19",{"date":330,"type":36},"2025-08-26",{"date":332,"type":36},"2024-08-23",{"date":303,"type":20},{"name":335,"class":43},"Gdansk University of Physical Education and Sport",{"id":337,"slug":338,"hasResults":11,"nctId":339,"briefTitle":340,"officialTitle":341,"acronym":4,"eligibilityCriteria":342,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":343,"targetDuration":4,"studyType":178,"phases":4,"briefSummary":345,"conditions":346,"keywords":354,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":361,"lastUpdatePostDateStruct":362,"startDateStruct":364,"completionDateStruct":366,"leadSponsor":368,"locationsCount":4},"100601744","addressing-pregnant-womens-first-trimester-worries-and-information-needs-with-mhealth-solutions-100601744","NCT07114471","Addressing Pregnant Women's First Trimester Worries and Information Needs With mHealth Solutions","Exploring the Anxieties and Health Information Needs of Women in the First Trimester to Inform mHealth Solutions for Antenatal Care","Pregnant women\n\nInclusion criteria\n\n* To ensure that participants have the first trimester of pregnancy fresh in their minds the sample will include women that are currently pregnant or have had a child within the last 2 years\n* Living in the UK\n* Over the age of 18\n* Able to give informed consent Exclusion criteria\n* Evidence of\u002Fdiagnosis of cognitive impairment\n\nHealthcare professionals\n\nInclusion criteria\n\n\\- Belonging to one of the following professional groups i.e. healthcare professionals involved in the care of pregnant women\n\n* Doctor in obstetrics and gynaecology\n* Midwives\n* Nurses (within the field of obstetrics and gynaecology),\n* Sonographers that scan pregnant women\n* General practitioners\n* Psychologists (that work with pregnant women)\n* Physiotherapists (that work with pregnant women)\n* Living in the UK\n* Over the age of 18\n* Able to give informed consent Exclusion criteria\n* Evidence of\u002Fdiagnosis of cognitive impairment\n\nDigital Health Experts\n\nInclusion criteria\n\n* Professionals with at least 3 year's experience in digital health, health informatics or mobile health application development\n* Based in the United Kingdom Exclusion criteria\n* Evidence of\u002Fdiagnosis of cognitive impairment",{"count":344,"type":20},1450,"The first 12 weeks of pregnancy, known as the first trimester, can be one of the most worrying times for women. (Where this lay summary refers to women, it should be taken to include people who do not identify as women but who have the capacity to become pregnant). Many experience nausea, bleeding, or anxiety about whether the pregnancy is progressing normally. Despite this, most women do not see a midwife or doctor until around 10 weeks into the pregnancy. This leaves a gap where they may have important questions but little professional support. As a result, many turn to mobile phone applications or the internet to find answers - but the quality of information online is mixed, and it can be confusing or even unsafe.\n\nThis research aims to understand what support women really need in early pregnancy, what concerns they have, and whether a mobile health application (mHealth app) could help fill this gap in current pregnancy care in a safe and personalised way. The study will also ask healthcare professionals and digital health experts what such an application should include, and how it can be made accessible, and easy to understand for all women - including those with different levels of health knowledge and digital skills.\n\nTo carry out the research, we will use a combination of online surveys and interviews. Women who are currently pregnant or have had a baby in the last two years will be invited to take part, along with healthcare professionals such as midwives and doctors, and experts in digital health. The survey will ask about their experiences in early pregnancy, how they have used digital tools or apps, and whether they felt their questions were answered before their first NHS appointment. The interview stage will allow participants to talk in more depth about what support they wanted and what would have helped them most. All participants will receive information about support services because we realise that discussing unmet information needs or worries in early pregnancy may be upsetting for some women.\n\nThe views collected will inform the design of a new mobile application to support women during early pregnancy. The application will use artificial intelligence (AI) to personalise information based on each woman's needs and background, and to explain things clearly and simply. The content and design of the application will be reviewed by doctors and digital health specialists to make sure it is safe, accurate, and easy to use.\n\nPublic and patient involvement is central to this project. A diverse group of women and representatives from grassroots organisations will be invited to shape the questions we ask, review the design of the application, and help us make it inclusive for people from different backgrounds.\n\nThis research will help us create a practical, trustworthy, and inclusive tool to support women during one of the most vulnerable times in pregnancy when women don't usually see a doctor. If successful, it could be used widely across the NHS to help reduce anxiety, improve understanding, and ensure women get the right support earlier in their pregnancy with the long-term aim of improving outcomes for women, babies, and families across the UK.",[347,348,349,27,350,351,352,353],"Pregnancy Trimester, First","Anxiety","Worries","mHealth Application","Mobile Application","Antenatal Care","Patient Education as Topic",[355,356,357,358,30,359,360],"Observational Study","Surveys and Questionnaires","Interview","Digital Health","Pregnant People","User Centered Design","2025-08-11",{"date":363,"type":36},"2025-08-14",{"date":365,"type":20},"2025-09",{"date":367,"type":20},"2027-10",{"name":369,"class":43},"Bournemouth University",{"id":371,"slug":372,"hasResults":11,"nctId":373,"briefTitle":374,"officialTitle":375,"acronym":4,"eligibilityCriteria":376,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":377,"enrollmentInfo":378,"targetDuration":4,"studyType":178,"phases":4,"briefSummary":380,"conditions":381,"keywords":383,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":388,"lastUpdatePostDateStruct":389,"startDateStruct":391,"completionDateStruct":393,"leadSponsor":395,"locationsCount":72},"100591304","the-validity-and-reliability-of-the-turkish-version-of-the-bbaq-100591304","NCT06978686","The Validity and Reliability of the Turkish Version of the BBAQ","The Validity and Reliability of the Turkish Version of the Barriers to Being Active Quiz","Inclusion Criteria:\n\n* Aged 18 years or older\n* Ability to read and write in Turkish\n* No visual or hearing impairments that would interfere with participation\n* Ability to follow simple instructions\n* Willingness to participate in the study\n\nExclusion Criteria:\n\n* Diagnosis of rheumatological conditions that may limit physical activity and are characterized by chronic inflammation and\u002For joint deformities (e.g., rheumatoid arthritis, ankylosing spondylitis, systemic lupus erythematosus, psoriatic arthritis)\n* Physical limitations due to neurological or orthopedic conditions (e.g., stroke, cerebral palsy, multiple sclerosis, limb amputation, or orthopedic surgery within the past six months)\n* History of psychiatric disorders that may impair cognitive functioning (e.g., schizophrenia, bipolar disorder, severe depression, attention deficit hyperactivity disorder)\n* Presence of any cognitive impairment","35 Years",{"count":379,"type":20},210,"The Barriers to Being Active Quiz (BBAQ) was originally developed in English to identify barriers to physical activity. This study aims to translate and cross-culturally adapt the BBAQ into Turkish (BBAQ-T) and evaluate its psychometric properties.",[27,382],"Physical Inactivity",[384,385,386,387],"exercise","questionnaires","physical activity","validation study","2025-06-15",{"date":390,"type":36},"2025-06-18",{"date":392,"type":36},"2025-05-20",{"date":394,"type":20},"2025-08-20",{"name":396,"class":43},"Istanbul Medeniyet University",{"id":398,"slug":399,"hasResults":11,"nctId":400,"briefTitle":401,"officialTitle":402,"acronym":4,"eligibilityCriteria":403,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":404,"targetDuration":4,"studyType":178,"phases":4,"briefSummary":406,"conditions":407,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":410,"lastUpdatePostDateStruct":411,"startDateStruct":412,"completionDateStruct":414,"leadSponsor":416,"locationsCount":44},"100594625","nlit-and-outcomes-in-hnc-survivor-caregiver-dyads-100594625","NCT07021885","NLit and Outcomes in HNC Survivor-Caregiver Dyads","Nutrition Literacy and Associated Outcomes in Head and Neck Cancer Survivor-caregiver Dyads","Inclusion Criteria:\n\n* Survivors and their caregivers will be eligible to participate if the survivor 1) has a history of oral cavity, pharyngeal, or laryngeal cancer, 2) is between 6 months - 4 years post-primary oncology treatment, 3) has no evidence of disease, 4) has an informal caregiver living in or out of the home who has a shared or primary role in food procurement and\u002For preparation, 5) no current use of feeding tube as the primary source of nutrition and can consume food orally, 6) age 18+, 7) English-speaking. Survivors and their caregivers will not be eligible to participate if either has 1) dementia or organic brain syndrome; 2) severe emotional distress; 3) active schizophrenia, 4) another diagnosis of cancer in the past five years (not including skin or cervical cancer in situ).\n\nExclusion Criteria:\n\n* Adults unable to consent\n* Individuals who are not yet adults (infants, children, teenagers)\n* Pregnant women\n* Prisoners",{"count":405,"type":20},150,"The goal of this observational (cross-sectional) study is to better understand nutrition literacy in survivor-caregiver dyads and its impact on nutrition related outcomes and quality of life. We're interested in finding out how much they know about nutrition and how this might relate to their overall health, body composition, functional status, and overall well-being. We will target post-treatment head and neck cancer survivors and a paired informal caregiver.\n\nThe main questions we aim to answer are:\n\n* How does the nutrition literacy of both the survivor and caregiver relate to their sociodemographic, behavioral, and clinical characteristics?\n* How dyadic nutrition literacy influence individual nutrition outcomes like skin carotenoid levels, body composition, and functional status?\n* Does the shared nutrition knowledge (nutrition literacy) of both the survivor and caregiver impact their quality of life together?\n\nParticipants will:\n\nAnswer questions about their knowledge of nutrition. Have their nutritional health status checked. Use a non-invasive device to measure skin carotenoid content to validate self-reports of fruit and vegetable intake.\n\nHave a simple and painless test to measure their body composition - like how much muscle and fat they have.\n\nDo some physical tests like grip strength and walking to measure their physical ability.\n\nAnswer questions about their general well-being and lifestyle, like exercise and diet.\n\n(For the survivor) Share details about their cancer, its treatment, and their overall well-being.\n\n(For the caregiver) Answer questions about their role in taking care of the survivor, and their involvement in care routine such as food shopping and cooking.",[408,409,27],"Head and Neck Cancer","Caregiver Burden","2025-06-11",{"date":388,"type":36},{"date":413,"type":36},"2023-12-01",{"date":415,"type":20},"2026-05-16",{"name":417,"class":43},"University of Kansas Medical Center",{"id":419,"slug":420,"hasResults":11,"nctId":421,"briefTitle":422,"officialTitle":423,"acronym":4,"eligibilityCriteria":424,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":267,"enrollmentInfo":425,"targetDuration":4,"studyType":21,"phases":427,"briefSummary":428,"conditions":429,"keywords":435,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":441,"lastUpdatePostDateStruct":442,"startDateStruct":444,"completionDateStruct":446,"leadSponsor":447,"locationsCount":72},"100557571","creating-a-new-health-promotion-module-to-help-the-indigenous-people-of-selangor-prepare-for-disease-x-and-outbreaks-100557571","NCT06539845","Creating a New Health Promotion Module to Help the Indigenous People of Selangor Prepare for Disease X and Outbreaks","Development and Effectiveness of a New Intervention on Household Preparedness for Disease X and Outbreaks Among Orang Asli in Selangor: A Cluster Randomized Trial","Inclusion Criteria:\n\n* Orang Asli ethnicity\n* Malaysian citizen\n* Age between 18 to 99 years old\n* The head of the household, or the person who contributes to, or influences health-related decisions for the household\n* Live in a household with at least three members\n* Able to converse in Malay\n\nExclusion Criteria:\n\n* Having physical or cognitive disabilities (e.g., blindness, deafness, schizophrenia and dementia)\n* Having severe health conditions (e.g., respiratory and cardiovascular disease requiring oxygen support such as severe asthma\u002Fchronic obstructive pulmonary disease\u002Fheart failure and congenital heart diseases)\n* Residing temporarily (less than 2 years)\n* Intending to relocate to a different residence within the next 2 years",{"count":426,"type":20},96,[23],"The goal of this cluster randomized trial is to develop and test a new method for preparing indigenous (locally termed as Orang Asli) households in Selangor, a state in Malaysia, for outbreaks and Disease X, a potential unknown infectious threat. It aims to determine if the new method, a health education package comprised of workshops, simulation exercises, and card game play sessions, can enhance the readiness of these families for such outbreaks.\n\nThe main questions it is looking to answer are:\n\n1. Will the intervention package increase the level of preparedness for a Disease X and outbreaks among indigenous households in Selangor?\n2. Will the intervention improve the awareness and attitudes of the indigenous people in Selangor towards outbreak preparedness?\n3. Will it lead to more proactive preparedness actions by these households?\n\nTo evaluate the effectiveness of the intervention package, researchers will compare outcomes between two groups: the intervention group receiving both the intervention package and educational brochures on communicable disease prevention, and the control group receiving only the brochures.\n\nParticipants will:\n\n1. Participate in the activities in the newly developed intervention package, which would include workshops, simulation exercises, and card game play sessions.\n2. Answer surveys four times: before, immediately after, 1 month after and 2 months after the intervention, to measure any changes in their preparedness levels for an outbreak.",[430,89,159,431,189,27,432,433,434],"Attitude to Health","Health-Related Behavior","Knowledge, Attitudes, Practice","Preparedness","Outbreaks",[436,437,433,438,439,440],"Indigenous People","Aboriginal","Readiness","Community Trial","Outbreak","2025-04-12",{"date":443,"type":36},"2025-04-16",{"date":445,"type":20},"2025-06",{"date":365,"type":20},{"name":448,"class":43},"Universiti Teknologi Mara",{"id":450,"slug":451,"hasResults":11,"nctId":452,"briefTitle":453,"officialTitle":453,"acronym":4,"eligibilityCriteria":454,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":455,"targetDuration":4,"studyType":178,"phases":4,"briefSummary":457,"conditions":458,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":461,"lastUpdatePostDateStruct":462,"startDateStruct":464,"completionDateStruct":466,"leadSponsor":468,"locationsCount":44},"100522348","public-survey-on-breath-testing-for-health-and-disease-100522348","NCT06081452","Public Survey on Breath Testing for Health and Disease","Inclusion Criteria:\n\n* Member of the public above the age of 18\n\nExclusion Criteria:\n\n* Member of the public below the age of 18",{"count":456,"type":20},1000,"A brief survey for the public to determine interest in health surveillance and disease detection",[459,460,159,189,431,27],"Cancer","Disease","2025-01-27",{"date":463,"type":36},"2025-01-28",{"date":465,"type":36},"2023-06-17",{"date":467,"type":20},"2025-10-17",{"name":469,"class":43},"Imperial College London",{"id":471,"slug":472,"hasResults":11,"nctId":473,"briefTitle":474,"officialTitle":475,"acronym":4,"eligibilityCriteria":476,"healthyVolunteers":15,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":477,"targetDuration":4,"studyType":21,"phases":479,"briefSummary":480,"conditions":481,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":484,"lastUpdatePostDateStruct":485,"startDateStruct":487,"completionDateStruct":489,"leadSponsor":491,"locationsCount":493},"100567946","school-based-e-health-non-communicable-disease-ncd-prevention-program-100567946","NCT06674798","School-based e-Health Non-Communicable Disease (NCD) Prevention Program","School-based e-Health Non-Communicable Disease (NCD) Prevention Program to Improve Awareness in Adolescents From Urban Pakistan","Inclusion Criteria:\n\nPhase 1 (FGDs and Interviews)\n\n* Students currently enrolled in secondary and higher secondary schools in Karachi and are in grades 9 to 12.\n* Teachers who have been employed in secondary and higher secondary schools in Karachi for a minimum duration of 6 months.\n* Parents or legal guardians of students who are currently enrolled in secondary and higher secondary schools in Karachi.\n* Principals and vice principals of secondary and higher secondary schools in Karachi, District Education Officers, and decision-makers at Provincial Department of Education.\n\nPhase 2 (Intervention)\n\n\\- Both study and control group would be selected from secondary schools (students in grades 9-10) and Higher Secondary Schools (students in grades 11-12) located in Karachi, Pakistan\n\nPhase 3 (FGDs) - Participants from grades 9 to 12 of the secondary and higher secondary schools who actively participated in the intervention and attended all the health-promoting sessions (equal representation of male and female)\n\nExclusion Criteria:\n\n\\- Schools outside Karachi",{"count":478,"type":20},272,[23],"The goal of this sequential mixed method study is to assess the feasibility and effectiveness of a school-based eHealth-NCD prevention program intervention to improve adolescents' knowledge, attitude, and practices regarding NCDs and associated risk factors. It aims :\n\n1. To identify barriers and facilitators associated with implementing a school-based eHealth intervention to improve the knowledge, attitudes, and practices of secondary and higher secondary school students in Pakistan regarding NCDs and their associated risk factors.\n2. To explore the stakeholders' perceptions regarding the design and content of the School based eHealth NCD prevention Program to improve the knowledge, attitudes, and practices of secondary and higher secondary school students in Pakistan regarding NCDs and their associated risk factors.\n3. To assess the feasibility and effectiveness of the School-based eHealth NCD prevention program in secondary and higher secondary school in Karachi.\n4. To evaluate the effectiveness of the school-based eHealth NCD prevention program in significantly improving the knowledge, attitudes, and practices of secondary and higher secondary school students in Karachi, Pakistan, regarding NCDs and their associated risk factors, as compared to a control group not receiving the intervention.\n5. To explore the perceptions of students regarding the usefulness acceptability and task technology fit of the School-based eHealth NCD prevention Program in improving the knowledge, attitude, and practices of Pakistani Higher Secondary School students regarding NCDs and their associated risk factors.\n\nResearcher aim to evaluate the effectiveness of the school-based eHealth NCD prevention program in significantly improving the knowledge, attitudes, and practices of secondary and higher secondary school students in Karachi, Pakistan, regarding NCDs and their associated risk factors, as compared to a control group not receiving the intervention.\n\nParticipants of intervention group will attend health-promoting sessions delivered by trained facilitators, with each session lasting 30 to 40 minutes. There will be a total of six health-promoting sessions be focused on the leading risk factors associated with NCDs as reported by different studies such as physical inactivity, unhealthy diet and overweight, obesity, harmful alcohol consumption and tobacco use will be conducted in the classroom for the intervention group.",[482,27,483],"Noncommunicable Diseases","Non-communicable Disease Risk Factors","2024-11-04",{"date":486,"type":36},"2024-11-05",{"date":488,"type":36},"2024-03-01",{"date":490,"type":20},"2025-03",{"name":492,"class":43},"Aga Khan University",7,{"id":495,"slug":496,"hasResults":11,"nctId":497,"briefTitle":498,"officialTitle":499,"acronym":500,"eligibilityCriteria":501,"healthyVolunteers":11,"sex":16,"minAge":502,"maxAge":503,"enrollmentInfo":504,"targetDuration":4,"studyType":21,"phases":505,"briefSummary":506,"conditions":507,"keywords":512,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":516,"lastUpdatePostDateStruct":517,"startDateStruct":519,"completionDateStruct":521,"leadSponsor":523,"locationsCount":44},"100562203","effect-of-educational-intervention-on-childrens-anxiety-100562203","NCT06600113","Effect of Educational Intervention on Children's Anxiety","Evaluating Effectiveness of Different Educational Methods on the Anxiety of Children Undergoing Anaesthesia - a Randomized Controlled Trial","MINA","Inclusion Criteria:\n\n* Undergoing anesthesia for medical procedure\n\nExclusion Criteria:\n\n* Does not understand Icelandic\u002FFinnish","4 Years","8 Years",{"count":405,"type":20},[23],"The aim of this randomized controlled trial is to evaluate the effectiveness of an educational health game intervention for children undergoing anesthesia from the perspective of children's anxiety. Participants are divided into three groups: one plays an educational game, another gets similar educational material (story) on a website and the third receives usual care. Anxiety will be evaluated with a standard assessment tool at the medical centre and parents answer questionnaires about themselves and their child. The study is an important step into innovation in the field of patient education where computer games are used to disseminate information, teach salvation and promote faith in the child's own ability and courage. The study will provide important information on children's anxiety for anaesthesia and what the effects of the computer game are compared to other educational methods.",[30,508,348,509,510,511,27],"Anesthesia","Fear","Attitude","Child Behavior",[513,514,508,515],"Children","Game","Health literacy","2024-09-12",{"date":518,"type":36},"2024-09-19",{"date":520,"type":36},"2022-11-21",{"date":522,"type":20},"2025-05-01",{"name":524,"class":43},"University of Iceland",{"id":526,"slug":527,"hasResults":11,"nctId":528,"briefTitle":529,"officialTitle":530,"acronym":4,"eligibilityCriteria":531,"healthyVolunteers":15,"sex":81,"minAge":532,"maxAge":238,"enrollmentInfo":533,"targetDuration":4,"studyType":21,"phases":535,"briefSummary":536,"conditions":537,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":332,"lastUpdatePostDateStruct":541,"startDateStruct":543,"completionDateStruct":545,"leadSponsor":547,"locationsCount":72},"100462203","faith-in-action-a-church-based-navigation-model-to-increase-breast-cancer-screening-in-korean-women-100462203","NCT05298605","Faith in Action! A Church-Based Navigation Model to Increase Breast Cancer Screening in Korean Women","Faith in Action! A Cluster-Randomized Trial to Evaluate the Efficacy of a Church-based Navigation Model to Increase Breast Cancer Screening Among Korean Women in Los Angeles","Inclusion Criteria:\n\n* Korean woman who is 45 years or older\n* Does not currently have a breast cancer diagnosis\n* Non-adherent to cancer screening (did not receive mammogram in last 2 years based on self-report)\n* Prospective or current member of participating Korean Churches\n* Willing to participate in study\n\nExclusion Criteria:\n\n* Does not meet inclusion criteria as described above","45 Years",{"count":534,"type":20},320,[23],"The purpose of this research is to develop a culturally adapted \"Faith in Action!\" curriculum to train lay health navigators to provide breast cancer screening navigation to Korean American women within faith-based settings and evaluate whether the culturally adapted \"Faith in Action!\" curriculum increases adherence to breast cancer screening guidelines among Korean American women within faith-based settings in Los Angeles, California. The primary research procedures include trainings and key informant interviews with lay health navigators in faith-based settings followed by a cluster randomized trial to evaluate the intervention.",[538,27,539,540],"Breast Cancer Female","Cancer Screening","Health Disparities",{"date":542,"type":36},"2024-08-27",{"date":544,"type":36},"2022-07-16",{"date":546,"type":20},"2025-12-01",{"name":283,"class":43},{"id":549,"slug":550,"hasResults":11,"nctId":551,"briefTitle":552,"officialTitle":552,"acronym":553,"eligibilityCriteria":554,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":555,"targetDuration":314,"studyType":178,"phases":4,"briefSummary":557,"conditions":558,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":575,"lastUpdatePostDateStruct":576,"startDateStruct":578,"completionDateStruct":580,"leadSponsor":582,"locationsCount":44},"100553518","virtual-peri-menopause-registry-of-australia-100553518","NCT06487130","Virtual perI-\u002FMenopause Registry of AusTrALia","VITAL","Inclusion Criteria:\n\n* Any Australian over 18 years of age.\n\nExclusion Criteria:\n\n* None.",{"count":556,"type":20},10000,"13 million (50.7%) Australians are born with ovaries, 14% (\\~3 million) are currently aged 40-59 yrs, \\& all such who live to midlife will experience menopause, defined as \\>12 months without a period. Peri-menopause (peri), typically occurs 5 yrs before menopause as hormone levels decrease. As with oestrogen, peri symptoms can affect every bodily system; e.g. depression\u002Fanxiety, diminished mental function, irregular periods, hot flushes, sleep problems, vaginal atrophy \\& urinary urgency. These symptoms are linked with lower quality of life \\& significantly higher work impairment; a third experiencing symptoms so severe as to impede daily life \\& increase risk of suicide. Lifetime increased risks of diabetes, heart disease, osteoporosis \\& dementia are also associated with menopause, yet it remains disconcertingly poorly studied.\n\nThe investigators propose to create a world-first, cutting-edge, consumer-driven, Virtual peri-\u002Fmenopause registry of AusTrALia (VITAL). The unique design will enable consumers to determine VITAL's questions, encourage secure revelation of private data e.g. vaginal \\& mental health symptoms, \\& to direct priorities for research, education, \\& health service improvements. VITAL will thus deliver optimal assessments of incidence, prevalence \\& impact.\n\nThe participating consumers, researchers, clinical specialists, policy makers, \\& modern virtual data infrastructure enable this unique \\& innovative registry design, future translation to improved community health, \\& promote awareness \\& collaborative synergies. Leveraging the investigators' critical range of expertise \\& ongoing feedback opportunities for both participants \\& stakeholder partnerships, the investigators will create a ground-breaking platform that:\n\n* empowers the consumer voice and priorities,\n* enables peri-\u002Fmenopause research to extend beyond existing niche focuses,\n* evidences the true impact of peri-\u002Fmenopause across the nation,\n* evolves healthcare services and outcomes, \\&\n* educates community, clinicians, \\& policy-makers. After Australian registry establishment, the investigators will expand VITAL to mirror it in other nations while still protecting individual's data the right way, but so all can learn \\& apply the best aspects of care from across the world.",[559,560,561,27,58,562,563,564,565,566,567,568,569,185,87,570,571,572,573,574],"Menopause","Perimenopausal Disorder","Postmenopausal Symptoms","Health Care Utilization","Health Care Seeking Behavior","Mental Health Impairment","Mental Deterioration","Mental Health Issue","Osteoporosis, Postmenopausal","Diabetes Mellitus Risk","Diabetes Mellitus, Type 2","Menopause Related Conditions","Hot Flashes","Hot Flushes Aggravated","Economic Burden","Social Stigma","2024-07-02",{"date":577,"type":36},"2024-07-05",{"date":579,"type":36},"2023-08-03",{"date":581,"type":20},"2073-08",{"name":583,"class":584},"Bespoke Clinical Research","INDUSTRY"]