[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"fear-anxiety\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:fear-anxiety":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,49,81,102],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100627821","effect-of-aiartificial-intelligence-based-storytelling-video-on-anxiety-and-fear-during-skin-prick-test-in-children-100627821",false,"NCT07453615","Effect of AI(Artificial Intelligence)-Based Storytelling Video on Anxiety and Fear During Skin Prick Test in Children","AI-Based Video-Mediated Cognitive Preparation in Skin Prick Testing: A Prospective, Randomized Controlled Trial","Inclusion Criteria:\n\n* Children aged between 4 and 10 years (from 4th birthday to 11th birthday).\n* Children undergoing a Skin Prick Test (SPT) for the first time.\n* Presence of suspected Allergic Rhinitis and\u002For Asthma.\n* Cognitive ability to understand Turkish, follow the video story, and interpret visual assessment scales.\n* Parents with internet access to view the digital content.\n* Obtained parental informed consent and child assent (for ages 7 and above)\n\nExclusion Criteria:\n\n* Previous experience with Skin Prick Testing or a history of frequent medical procedures (e.g., frequent blood draws, surgeries) due to chronic illness.\n* Diagnosed with Autism Spectrum Disorder, severe ADHD(attention deficit hyperactivity disorder), intellectual disability, or severe psychiatric conditions preventing cooperation.\n* Significant visual or hearing impairments that prevent engagement with the video content.\n* Use of anxiolytics, sedatives, or medications affecting cognitive functions within the last 24 hours.\n* Chronic health problems (e.g., malignancy, immunodeficiency) that may elevate baseline anxiety levels.\n* Patients undergoing SPT for suspected Food Allergy, Drug Allergy, or Bee Venom Allergy.\n* For the intervention group: Failure to watch the video or answering the three \"validation questions\" incorrectly on the procedure day.","ALL","4 Years","10 Years",{"count":20,"type":21},100,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study evaluates the effectiveness of an AI-generated therapeutic storytelling video on pre-procedural anxiety and fear levels in children aged 4 to 10 years undergoing their first Skin Prick Test (SPT). The study aims to determine if watching a cognitive preparation video at home prior to the appointment reduces anxiety compared to standard care. Participants will be randomized into two groups: an intervention group watching the AI-generated video and a control group receiving standard clinic care",[27,28,29,30],"Anxiety","Fear Anxiety","Allergic Rhinitis","Asthma (Diagnosis)",[32,33,34,35],"Skin Prick Test","Artificial Intelligence","Cognitive Preparation","Storytelling","RECRUITING","2026-03-16",{"date":39,"type":40},"2026-03-18","ACTUAL",{"date":42,"type":40},"2026-03-15",{"date":44,"type":21},"2026-09-15",{"name":46,"class":47},"Antalya Training and Research Hospital","OTHER_GOV",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":55,"sex":16,"minAge":56,"maxAge":57,"enrollmentInfo":58,"targetDuration":4,"studyType":22,"phases":60,"briefSummary":61,"conditions":62,"keywords":65,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":4},"100615934","the-effect-of-a-guessing-game-on-fear-pain-and-emotional-state-during-blood-collection-in-children-aged-6-12-100615934","NCT07299058","The Effect of a Guessing Game on Fear, Pain, and Emotional State During Blood Collection in Children Aged 6-12","Inclusion Criteria:\n\n* Being between 6 and 12 years of age\n* Not having a previous diagnosis of a serious hematological\u002Fpsychiatric disease\n* The child and parent must be willing to participate in the study\n* Being able to speak and understand Turkish\n\nExclusion Criteria:\n\n* Having received sedation, analgesics, or anxiolytic medication during the procedure\n* Having a visual\u002Fhearing impairment\n* Having previously undergone an invasive procedure on the same day",true,"6 Years","12 Years",{"count":59,"type":21},70,[24],"The aim of this study is to evaluate the effects of a guessing game on fear, pain and emotional state during blood collection in children aged 6-12 years.",[63,64,28],"Pain","Blood Sampling Procedure",[66,67,68,69],"pain","fear","emotional state","children","NOT_YET_RECRUITING","2025-12-09",{"date":73,"type":40},"2025-12-23",{"date":75,"type":21},"2025-12-20",{"date":77,"type":21},"2026-12-31",{"name":79,"class":80},"Dokuz Eylul University","OTHER",{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":4,"eligibilityCriteria":87,"healthyVolunteers":55,"sex":16,"minAge":17,"maxAge":56,"enrollmentInfo":88,"targetDuration":4,"studyType":22,"phases":90,"briefSummary":91,"conditions":92,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":48},"100583297","inhalation-treatment-distraction-in-children-100583297","NCT06874491","Inhalation Treatment Distraction in Children","Effects of Two Different Distraction Methods on Fear and Anxiety Levels in Preschool Children Receiving Inhalation Treatment","Inclusion Criteria:\n\n* -Being between 4-6 years old\n* Not having a developmental disability\n* Not having a history of sedative, analgesic or narcotic substance use within 24 hours before application\n* Receiving inhalation therapy for the first time\n* Not having a chronic disease\n* Children who are accompanied by their mother or father during the procedure will be included in the study.\n\nExclusion Criteria:\n\n* Being under 4 years old or over 6 years old\n* having a chronic disease",{"count":89,"type":21},126,[24],"The aim of the project is to examine the effects of two different distraction methods used in preschool children receiving inhalation therapy on fear and anxiety levels. Children are exposed to various hospital procedures throughout their lives. These procedures cause children to experience fear, pain and anxiety. One of these procedures is inhalation therapy. When children wear the face masks required for inhalation, they experience intense fear and anxiety. Non-pharmacological techniques are used for the effective management of this fear and anxiety. Among these techniques, distraction is the easy-to-apply. When applying distraction techniques, the child's developmental period, age group and interest should be taken into consideration. The project is a randomized controlled trial. The universe of the study will consist of children between the ages of 4-6 who received inhalation therapy for the first time in the pediatric emergency department of Erzincan Mengücek Gazi Education and Research Hospital between September 2025 and September 2026. In collecting the research data, \"Questionnaire Form\", \"Child Fear Scale\" and \"Child Anxiety Scale-State\" will be used.\n\nThe two different methods to be used will be designed to attract the attention and interest of the age groups of the children to be included in the research. In this way, it is thought that the child will focus his\u002Fher attention and curiosity on the two different methods to be used and the level of fear and anxiety will be affected during the inhalation treatment. This will increase the child's compliance and cooperation with the treatment and will encourage the child.\n\nWhen the international and national literature was scanned, no study was found that investigated the effects of the two different distraction methods covered in the research during inhalation treatment. With the two different distraction methods to be used, inhalation treatment, which is a source of fear and anxiety for children, will become fun.",[28],"2025-10-02",{"date":95,"type":40},"2025-10-07",{"date":97,"type":40},"2025-09-01",{"date":99,"type":21},"2026-09-25",{"name":101,"class":80},"Ataturk University",{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":4,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":16,"minAge":109,"maxAge":4,"enrollmentInfo":110,"targetDuration":4,"studyType":112,"phases":4,"briefSummary":113,"conditions":114,"keywords":117,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":121,"lastUpdatePostDateStruct":122,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":48},"100569025","the-study-is-about-the-inuence-of-the-combination-of-music-and-noise-cancelling-as-a-non-pharmacological-aid-in-reducing-anxiety-and-discomfort-during-wisdom-tooth-removal-the-level-of-fear-is-measured-by-a-questionnaire-which-the-patients-answer-twice-and-a-measurement-of-the-heartbeat-100569025","NCT06688877","The Study is About the influence of the Combination of Music and Noise Cancelling as a Non-pharmacological Aid in Reducing Anxiety and Discomfort During Wisdom Tooth Removal. The Level of Fear is Measured by a Questionnaire Which the Patients Answer Twice and a Measurement of the Heartbeat","Einfluss Der Kombination Von Musik Und Noise Cancelling Als nichtmedikamentöse Unterstützung Bei Angst Und Unwohlsein während Der Weisheitszahnentfernung","Inclusion Criteria:\n\n* willing to participate in the clinical trial, understood and signed the information sheet\n\nExclusion Criteria:\n\n* younger than 18 years old\n* hearing impairment","18 Years",{"count":111,"type":21},156,"OBSERVATIONAL","The goal of this clinical trial is to learn if the reduction of the noises (through head phones with music and noise cancelling) that occur during wisdom teeth removal, leads to a significant reduction in fear levels in patients compared to patients who do not have any noise reduction. The main questions it aims to answer are:\n\nDo music and noise cancelling help patients to have less fear during wisdom teeth removal surgery by reducing the sounds of the surgery? Is there a difference between just the noise cancelling function or is it better to combine noise cancelling and music together?\n\nParticipants will:\n\nJust come to their regular appointment (wisdom teeth removal) to our clinic, no follow ups needed. All participants will answer one questionnaire before and one after the surgery. All of them will have their rate of heartbeat measured for three times (before, during and after surgery, measured by a puls oximeter on the finger). They will be allocated to one of the three study groups (no headphones, headphones with noise cancelling or headphones with noise cancelling and music).",[28,115,116],"Wisdom Tooth Removal","Heart Rate",[118,119,120],"fear level","wisdom teeth removal","noise reduction by music and noise cancelling","2024-11-13",{"date":123,"type":40},"2024-11-14",{"date":125,"type":21},"2024-11-18",{"date":127,"type":21},"2025-06-29",{"name":129,"class":80},"Sigmund Freud PrivatUniversitat"]