[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"awareness\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:awareness":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,51,82,114,146,174,194,226],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":32,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100640077","trauma-informed-yoga-intervention-in-young-women-100640077",false,"NCT07589777","Trauma-Informed Yoga Intervention in Young Women","Trauma-Informed Yoga Intervention: A Randomized Controlled Trial on Psychological Trauma, Emotion Regulation, and Interoceptive Awareness in Young Adult Women","Inclusion Criteria:\n\n* Being a woman aged 18-25 years\n* Providing voluntary written informed consent after being informed about the study\n* Scoring within the highest 25th percentile on the Transmitted Psychological Trauma Scale based on the pre-screening assessment, indicating high levels of trauma-related symptoms\n* Having no physical limitations that would prevent participation in weekly sessions and being medically eligible to engage in yoga practices\n* Agreeing to comply with the study protocol, including attendance at intervention sessions and completion of all assessments\n\nExclusion Criteria:\n\n* Inability to provide reliable responses due to the presence of active psychotic disorder, bipolar disorder, or severe cognitive impairment\n* Being in an acute psychological crisis\n* Initiation of intensive psychotherapy targeting trauma symptoms (e.g., trauma-focused therapy) within the past 3 months or participation in a similar structured psychosocial intervention during the study period\n* Presence of serious musculoskeletal, cardiovascular, or neurological conditions or injuries that would prevent participation in yoga, or medical restriction of physical activity by a physician\n* Having an established regular practice of yoga or meditation",true,"FEMALE","18 Years","25 Years",{"count":21,"type":22},46,"ESTIMATED","INTERVENTIONAL",[25],"NA","The aim of this study is to evaluate the effects of a trauma-informed yoga intervention on psychological trauma symptoms, difficulties in emotion regulation, and interoceptive awareness in young adult women.",[28,29,30,31],"Trauma","Young Adult Females","Awareness","Emotional Regulation",[33,34,35,36,37],"trauma-informed yoga","emotion regulation","interoceptive awareness","psychological trauma","randomized controlled trial","NOT_YET_RECRUITING","2026-05-09",{"date":41,"type":42},"2026-05-15","ACTUAL",{"date":44,"type":22},"2026-06-01",{"date":46,"type":22},"2026-11-30",{"name":48,"class":49},"Saglik Bilimleri Universitesi","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":57,"eligibilityCriteria":58,"healthyVolunteers":16,"sex":17,"minAge":59,"maxAge":4,"enrollmentInfo":60,"targetDuration":4,"studyType":23,"phases":62,"briefSummary":63,"conditions":64,"keywords":69,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":81},"100634605","breast-and-cervical-cancer-awareness-training-in-visually-impaired-women-100634605","NCT07541859","Breast and Cervical Cancer Awareness Training in Visually Impaired Women","The Effect of Awareness Education on Breast and Cervical Cancer Screening Among Visually Impaired Women","GORSEM","Eligibility Criteria\n\nInclusion Criteria:\n\n* Women with only a visual impairment (congenital or acquired)\n* Able to communicate, speak, and understand Turkish\n* Voluntarily agree to participate in the study\n* Over the age of 40\n* Have had previous sexual intercourse (Pap smear screening requires sexual activity)\n\nExclusion Criteria:\n\n* Diagnosed with breast or cervical cancer\n* Under the age of 40\n* Have not had sexual intercourse before\n* Have undergone screening for at least one of these two cancer types (breast or cervical) within the last year\n\nAccording to the Turkish Ministry of Health, General Directorate of Public Health, in current screenings conducted in our country, within the breast cancer screening program for women, mammography is recommended every two years for women aged 40-69, and within the cervical cancer screening program, Pap smear and HPV-DNA tests are recommended every five years for women aged 30-65. Since women will be referred by the researchers to KETEM centers after training to undergo mammography and Pap smear screening tests, visually impaired women over the age of 40 who have previously had sexual intercourse will be included in the study, as these two screening tests are performed in this common age group and Pap smear screening requires being sexually active.","40 Years",{"count":61,"type":22},74,[25],"This quasi-experimental study aims to determine whether a breast and cervical cancer awareness training program can increase participation in cancer screening among women with visual impairments. The study also aims to identify barriers to screening and improve knowledge about cancer risk factors and screening methods. The main questions this study will address are:\n\n* Does the training increase the rate at which women with visual impairments attend cancer screening appointments?\n* Does the training improve participants' knowledge about breast and cervical cancer?\n\nParticipants will:\n\n* Receive training on breast and cervical cancer risk factors and screening methods.\n* Learn how to apply to the Cancer Early Diagnosis, Screening, and Training Center.\n* Be encouraged to attend cancer screening during the study period.\n* Have knowledge and screening status assessed before the training, immediately after, and three months later.",[65,66,67,30,68],"Persons With Visual Disabilities","Breast Neoplasms","Uterine Cervical Neoplasms","Early Detection of Cancer",[70,71,67,66],"Cancer Screening","Visual Impairment Awareness","2026-04-14",{"date":74,"type":42},"2026-04-21",{"date":76,"type":22},"2026-06",{"date":78,"type":22},"2026-12",{"name":80,"class":49},"Marmara University",2,{"id":83,"slug":84,"hasResults":11,"nctId":85,"briefTitle":86,"officialTitle":87,"acronym":88,"eligibilityCriteria":89,"healthyVolunteers":16,"sex":90,"minAge":18,"maxAge":91,"enrollmentInfo":92,"targetDuration":4,"studyType":23,"phases":94,"briefSummary":95,"conditions":96,"keywords":100,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":105,"lastUpdatePostDateStruct":106,"startDateStruct":108,"completionDateStruct":110,"leadSponsor":112,"locationsCount":50},"100633071","child-abuse-and-neglect-awareness-training-in-nursing-students-100633071","NCT07521917","Child Abuse and Neglect Awareness Training in Nursing Students","Effect of Child Abuse and Neglect Awareness Training on Nursing Students: A Randomized Controlled Trial","CANAT","Inclusion Criteria:\n\n* Being an undergraduate nursing student\n* Being able to read and understand Turkish\n* Willingness to participate in the study\n* Providing written informed consent\n\nExclusion Criteria:\n\n* Not completing the training program\n* Not completing the pre-test or post-test\n* Withdrawing from the study at any stage","ALL","30 Years",{"count":93,"type":22},120,[25],"This randomized controlled study aims to evaluate the effect of a child abuse and neglect awareness training program on the knowledge and awareness levels of nursing students. Child abuse and neglect remain significant global public health issues, and healthcare professionals, particularly nurses, play a key role in early recognition and intervention.\n\nThe study will be conducted among undergraduate nursing students at a university in Istanbul, Turkey. Participants will be randomly assigned to either an experimental group or a control group. Both groups will complete a pre-test to assess baseline knowledge levels. The experimental group will receive a structured training program on child abuse and neglect delivered by an expert nurse working at a Child Advocacy Center under the Ministry of Health, while the control group will not receive any intervention during the study period.\n\nOne month after the intervention, both groups will complete a post-test to assess changes in knowledge and awareness levels. The primary outcome of the study is the difference in awareness test scores between the pre-test and post-test. The findings are expected to contribute to improving educational strategies and enhancing the competencies of future nurses in recognizing and managing child abuse and neglect cases.",[97,98,30,99],"Child Abuse","Child Neglect","Nursing Education",[101,102,103,104],"Nursing students","Child abuse","Child neglect","Awareness training","2026-04-11",{"date":107,"type":42},"2026-04-15",{"date":109,"type":22},"2026-04-01",{"date":111,"type":22},"2026-06-30",{"name":113,"class":49},"Istanbul Arel University",{"id":115,"slug":116,"hasResults":11,"nctId":117,"briefTitle":118,"officialTitle":119,"acronym":120,"eligibilityCriteria":121,"healthyVolunteers":11,"sex":90,"minAge":18,"maxAge":4,"enrollmentInfo":122,"targetDuration":4,"studyType":23,"phases":124,"briefSummary":125,"conditions":126,"keywords":130,"overallStatus":135,"whyStopped":4,"lastUpdateSubmitDate":136,"lastUpdatePostDateStruct":137,"startDateStruct":139,"completionDateStruct":141,"leadSponsor":143,"locationsCount":145},"100480304","the-ed-awareness-2-trial-100480304","NCT05534243","The ED-AWARENESS-2 Trial","Awareness With Paralysis and Post-Traumatic Stress Disorder Among Mechanically Ventilated Emergency Department Survivors: the ED-AWARENESS-2 Trial","ED-AWARENES II","Inclusion Criteria:\n\n1. Mechanical ventilation via an endotracheal tube\n2. Age ≥ 18 years\n3. Treatment with a neuromuscular blocker (for endotracheal intubation or during the post-intubation phase of care)\n\nExclusion Criteria:\n\n1. Acute or chronic neurologic injury with deficit that prevents assessment of AWP (i.e. stroke, intracranial hemorrhage, traumatic brain injury, cardiac arrest, severe dementia)\n2. Death before extubation\n3. Transfer to another hospital from the ED",{"count":123,"type":22},3090,[25],"The investigators will screen all mechanically ventilated ED patients for study eligibility and will enroll all consecutive patients satisfying inclusion and exclusion criteria.\n\nThe study design is a pragmatic, multicenter, stepped wedge cluster randomized trial, enrolling at five sites over a 3-year period, divided into six time periods of six months. Prior to the study, each site will be randomized to their position within the design. One site will cross to the intervention period (i.e. succinylcholine as default neuromuscular blocker) every six months from the 2nd to 6th time period. Cluster order will be determined by computer-based randomization. To begin, each site will be exposed to control conditions; by the end of the study, each site will be exposed to intervention conditions.\n\nPatients in the control phase will receive usual care, and this phase will be entirely observational. After six months, a site will enter a 2-month transition phase. In this phase, the investigators will implement the intervention, similar to how they have implemented other ED-based interventions for mechanically ventilated patients. The investigators will engage and educate ED clinicians on the importance of AWP prevention and the study objectives. The intervention framework relies on the use of \"nudges\", without restricting choice. The use of neuromuscular blockers (i.e. \"paralytic\" medications) is already part of routine care in the ED in order to facilitate endotracheal intubation and initiation of mechanical ventilation for patients with acute respiratory failure. The two most common neuromuscular blockers used in the ED are succinylcholine and rocuronium. The preliminary data show a strong association between rocuronium (a longer-acting neuromuscular blocker) use and AWP. Therefore, this study aims to improve care by educating caregivers on AWP and the use of the neuromuscular blockers, which are already routinely used, and studying that process in a rigorous fashion. The default neuromuscular blocker in the intervention phase will be succinylcholine. Succinylcholine will be the default over rocuronium because: 1) it has safely been the default neuromuscular blocker of choice in the ED for \\>40 years ; 2) its 5-minute duration of action greatly reduces AWP risk; 3) the preliminary data regarding an increased risk of AWP with rocuronium and 4) ED rocuronium use has increased despite no patient-centered studies showing benefit over succinylcholine. Passive alerts (i.e. graphics, pocket cards) will also be strategically placed in the ED, and active alerts will be used as reminders before every nursing shift (i.e. \"the huddle\"). After this transition phase, the site will begin the intervention phase, and patients will again receive clinician-directed care, just after the intervention.",[30,127,128,129],"Mechanical Ventilation","Intubation Complication","PTSD",[30,131,132,133,127,134],"Paralysis","Emergancy Department","Rocuronium","Intubation","RECRUITING","2026-03-09",{"date":138,"type":42},"2026-03-12",{"date":140,"type":42},"2023-06-28",{"date":142,"type":22},"2027-09-01",{"name":144,"class":49},"Washington University School of Medicine",4,{"id":147,"slug":148,"hasResults":11,"nctId":149,"briefTitle":150,"officialTitle":151,"acronym":152,"eligibilityCriteria":153,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":154,"enrollmentInfo":155,"targetDuration":4,"studyType":23,"phases":157,"briefSummary":158,"conditions":159,"keywords":164,"overallStatus":135,"whyStopped":4,"lastUpdateSubmitDate":165,"lastUpdatePostDateStruct":166,"startDateStruct":168,"completionDateStruct":170,"leadSponsor":172,"locationsCount":50},"100620796","mat-pilates-on-body-awareness-and-physical-activity-levels-in-sedentary-emerging-adulthood-women-100620796","NCT07362277","Mat Pilates on Body Awareness and Physical Activity Levels in Sedentary Emerging Adulthood Women","The Effect of Mat Pilates on Body Composition and Physical Activity Levels in Sedentary Women Emerging Adulthood","mat pilates","Inclusion Criteria:\n\n* Possess the ability to read and understand Turkish, be between the ages of 18 and 29,\n* I have a sedentary lifestyle, possess the cognitive ability to understand and interpret survey questions, and for sedentary participants, not have engaged in regular exercise for 2 months, have a Physical Activity Score (IPAQ) -short form of less than 600 Metabolic Equivalent of Task (MET) minutes per week, and body weight below 130 kg.\n\nExclusion Criteria:\n\n* Participants with chronic, neurological, orthopedic, rheumatic systemic and\u002For lung disease, those who exercise\u002Fsport, have a history of malignancy, are pregnant, have a history of fracture in the last year,\n* I have chronic kidney or liver disease, have cardiovascular disease, and have peripheral vestibular disorder were excluded.","29 Years",{"count":156,"type":22},54,[25],"This study investigating the effects of mat pilates on body awareness and physical activity levels in sedentary women transitioning to adulthood, 27 control groups and 27 mat pilates exercise groups will be included. The groups will be compared at the end of an 8-week exercise program. Participants' socio-demographic characteristics, body awareness (using the Body Awareness Questionnaire), and physical activity level (using the Tegner Physical Activity Questionnaire and the International Physical Activity Questionnaire short-form scales) will be assessed.",[160,30,161,162,163],"Exercise Therapy","Sedentary Behavior","Woman's Role","Exercise",[160,30,161,162,163],"2026-01-22",{"date":167,"type":42},"2026-01-23",{"date":169,"type":42},"2025-12-05",{"date":171,"type":22},"2026-02-20",{"name":173,"class":49},"Necmettin Erbakan University",{"id":175,"slug":176,"hasResults":11,"nctId":177,"briefTitle":178,"officialTitle":179,"acronym":4,"eligibilityCriteria":180,"healthyVolunteers":16,"sex":90,"minAge":18,"maxAge":4,"enrollmentInfo":181,"targetDuration":4,"studyType":183,"phases":4,"briefSummary":184,"conditions":185,"keywords":4,"overallStatus":135,"whyStopped":4,"lastUpdateSubmitDate":187,"lastUpdatePostDateStruct":188,"startDateStruct":189,"completionDateStruct":191,"leadSponsor":192,"locationsCount":50},"100613462","impact-of-attentional-tunelling-on-a-population-of-french-practitioners-100613462","NCT07266909","Impact of Attentional Tunelling on a Population of French Practitioners","Impact of Attentional Tunneling or the \"Tunnel Effect\" in Dentistry. Multi-centre Cross-sectional Study of a Population of French Practitioners.","Inclusion Criteria:\n\n* University hospital practitioner (professor, associate professor, ...)\n* Dental surgeon (outside university hospitals\n* Intern (DES MBD and ODF).\n\nExclusion Criteria:\n\n* Students.",{"count":182,"type":22},160,"OBSERVATIONAL","The tunnel effect, also known as attentional tunnelling, is a cognitive bias affecting all healthcare professionals, including odontologists. It is characterised by an excessive focus on a specific element of a clinical situation, which can alter the overall assessment and lead to errors in medical practice. This poses a particular risk to the quality of dental care, especially surgical care. Despite the importance of this risk, few studies have addressed this issue in dentistry. Therefore, raising the dental community's awareness of this phenomenon on a large scale is both justified and necessary.",[30,186],"Attention","2025-11-25",{"date":169,"type":42},{"date":190,"type":42},"2025-11-21",{"date":46,"type":22},{"name":193,"class":49},"Centre Hospitalier Universitaire de Nice",{"id":195,"slug":196,"hasResults":11,"nctId":197,"briefTitle":198,"officialTitle":199,"acronym":200,"eligibilityCriteria":201,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":59,"enrollmentInfo":202,"targetDuration":4,"studyType":23,"phases":204,"briefSummary":205,"conditions":206,"keywords":211,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":217,"lastUpdatePostDateStruct":218,"startDateStruct":220,"completionDateStruct":222,"leadSponsor":224,"locationsCount":50},"100565313","the-effect-ofgreen-future-with-midwife-handsclimate-change-animation-on-mothers-climate-change-awareness-and-behavior-100565313","NCT06640556","The Effect of\"Green Future With Midwife Hands\"Climate Change Animation on Mothers' Climate Change Awareness and Behavior","The Effect of \"Green Future With Midwife Hands\" Climate Change Animation on Mothers' Climate Change Awareness and Behavior","RKÇ","Inclu• Pregnant women who can read and write Turkish,\n\n* Volunteer to participate in the research,\n* Have had a normal or cesarean delivery,\n* Are primiparous,\n* Are open to communication (able to understand and answer questions) will be included in the samplesion Criteria:\n\nExclusion Criteria:\n\n* • Those who do not have the ability to read, listen, write, speak and understand Turkish,\n\n  * Those who have hearing or visual impairments,\n  * Those who have postpartum complications,\n  * Those who have had a stillbirth,\n  * Those who wish to withdraw from the study were not included.",{"count":203,"type":22},666,[25],"The Effect of \"Green Future with Midwife Hands\" Climate Change Animation on Mothers' Climate Change Awareness and Behavior Climate change appears as one of the most important environmental problems of today. Many negative effects such as the increase in greenhouse gas emissions, global warming, sea level rise and the frequency of extreme weather events threaten both natural ecosystems and human life. In this context, it is of great importance for individuals to gain awareness about climate change and exhibit environmentally friendly behavior for a sustainable future. In particular, mothers and expectant mothers have the potential to create significant awareness and change by choosing products that do not harm the environment, while looking for the best for their babies. Reducing plastic use, choosing organic textile products, using biodegradable wet wipes and choosing toys made from natural materials both protect babies' health and support environmental sustainability. This awareness reinforces the environmentally friendly behavior of mothers and helps future generations grow up as more conscious individuals. The role of mothers in this regard is undeniably great for a sustainable future. While mothers making environmentally friendly choices increases the environmental awareness of not only their own families but also the wider masses, being careful when choosing carbon footprint baby products both protects the health of babies and reduces environmental impacts.\n\nThis research aims to encourage mothers and expectant mothers to make environmentally friendly and carbon footprint-reducing choices when choosing baby products by increasing the climate change awareness of mothers and expectant mothers through the \"Green Future with Midwife Hands\" Climate Change Animation.",[207,30,208,209,210],"Climate Change","Conscious","Consumption","Consumption Habits of Mothers",[212,213,214,215,216],"Climate change","awareness","conscious","consumption","consumption habits of mothers","2025-09-09",{"date":219,"type":42},"2025-09-15",{"date":221,"type":22},"2025-09-10",{"date":223,"type":22},"2025-10-01",{"name":225,"class":49},"KTO Karatay University",{"id":227,"slug":228,"hasResults":11,"nctId":229,"briefTitle":230,"officialTitle":231,"acronym":4,"eligibilityCriteria":232,"healthyVolunteers":11,"sex":90,"minAge":18,"maxAge":4,"enrollmentInfo":233,"targetDuration":4,"studyType":183,"phases":4,"briefSummary":235,"conditions":236,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":237,"lastUpdatePostDateStruct":238,"startDateStruct":240,"completionDateStruct":242,"leadSponsor":244,"locationsCount":4},"100582907","awareness-of-patients-having-diabetes-mellitus-about-oral-health-100582907","NCT06869421","Awareness of Patients Having Diabetes Mellitus About Oral Health","Knowledge, Attitude and Awareness of Diabetic Patients on Association Between Oral Health and Diabetes Mellitus","Inclusion Criteria:\n\n* aged at least 18 years and being diagnosed with diabetes mellitus\n\nExclusion Criteria:\n\n* individuals who refuse to participate in the study",{"count":234,"type":22},310,"Diabetic patients will be asked to answer a group of questions about the predictors (age, type of diabetes, level of education) and about the outcomes \\[knowledge and awareness of the link between diabetes and oral health, and attitude towards maintaining their oral health as diabetics.",[30],"2025-03-05",{"date":239,"type":42},"2025-03-11",{"date":241,"type":22},"2025-03",{"date":243,"type":22},"2025-09",{"name":245,"class":49},"Cairo University"]