[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"distraction-methods\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:distraction-methods":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,48,79],{"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":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100632635","effects-of-cartoons--interactive-storytelling-on-fear-and-comfort-in-6-9-year-olds-during-nebulizer-treatment-100632635",false,"NCT07516249","Effects of Cartoons & Interactive Storytelling on Fear and Comfort in 6-9 Year Olds During Nebulizer Treatment","The Effect of Cartoon Viewing and Breath-Synchronized Interactive Storytelling During Nebulizer Medication Administration on Fear, Emotional Behavior, and Comfort in 6-9 Year Old Children: A Randomized Controlled Study","Inclusion Criteria:\n\n* \\- Children aged 6-9 years\n* Scheduled to receive nebulizer inhalation therapy due to acute or chronic respiratory disease\n* Conscious, responsive to environmental stimuli, and able to communicate verbally or nonverbally\n* Without a diagnosed neurodevelopmental disorder (severe autism spectrum disorder, severe intellectual disability, etc.)\n* Without severe hearing or vision loss that would impair storytelling and visual material comprehension\n* Without signs of respiratory failure requiring emergency intervention during nebulizer administration\n* With written informed consent from a parent or legal guardian\n* Children who are willing to participate in the study after being given explanations appropriate to their age and developmental level.\n\nExclusion Criteria:\n\n* Patients who require emergency medical intervention during nebulizer application, such as severe respiratory distress, cyanosis, or significantly low oxygen saturation.\n* Patients who are unconscious or unable to respond adequately to environmental stimuli.","ALL","6 Years","9 Years",{"count":20,"type":21},96,"ESTIMATED","INTERVENTIONAL",[24],"NA","Fear and anxiety experienced by children during inhalation therapy (using a nebulizer or vaporizer) are key factors that make treatment compliance difficult and reduce the quality of care. Young children, in particular, may perceive this process as \"threatening\" due to mask use, the noise produced by the device, and a sense of loss of control. This situation triggers a significant physiological stress response in the child.\n\nTherefore, in pediatric nursing, non-pharmacological methods that increase children's participation in treatment are of great importance. The literature indicates that interventions such as showing cartoons, playing music, and using distracting visual materials both reduce anxiety and improve stress indicators like heart rate. Additionally, therapeutic play has been proven to help children adapt to the hospital environment and soothe their emotional reactions.\n\nThis study aims to evaluate the effectiveness of a nursing intervention-designed to enhance children's physical comfort and manage their fear and anxiety during inhalation therapy-that is breath-synchronized, interactive, and story-based.",[27,28],"Distraction Methods","Nursing Care",[30,31,32,33,34],"Administration, Inhalation","Distraction methods","fear","comfort","cartoon","NOT_YET_RECRUITING","2026-04-02",{"date":38,"type":39},"2026-04-07","ACTUAL",{"date":41,"type":21},"2026-04-23",{"date":43,"type":21},"2026-10-30",{"name":45,"class":46},"Mersin University","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":16,"minAge":56,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":64,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":47},"100607765","the-effect-of-attention-distraction-on-the-adherence-to-exercise-in-chronic-low-back-pain-patients-100607765","NCT07192809","The Effect of Attention Distraction on the Adherence to Exercise, in Chronic Low Back Pain Patients.","Chronic Non-Specific Low Back Pain: Investigating the Effectiveness of a Dual-Task Program as an Attention Distraction Strategy","PAINLESS","Inclusion Criteria:\n\n* Age \\> 18 years\n* Chronic non-specific low back pain (≥3 months)\n* No physical therapy or structured exercise program in the last 3 months\n* Willingness to use the attention distraction application (for the AD-APP group)\n* Completion of the International Physical Activity Questionnaire (IPAQ)\n\nExclusion Criteria:\n\n* History of spinal surgery\n* Neurological conditions affecting movement\n* Regular use of pain relief medication within the past two weeks\n* Pregnancy\n* Severe psychological disorders that may affect compliance","18 Years",{"count":58,"type":21},60,[24],"This randomized controlled trial aims to investigate whether the use of an attention distraction application during exercise increases patient adherence to exercise programs in chronic non-specific low back pain (CNSLBP). In addition, the study will examine whether higher adherence to exercise leads to improved outcomes in pain levels, functional capacity, kinesiophobia, quality of life, central sensitization, and pain catastrophizing.",[62,27,63],"Chronic Low Back Pain (CLBP)","Adherence to Care",[65,66,67,68,69],"chronic low back pain","adherence","distraction","divided attention","chronic non specific low back pain","2025-09-17",{"date":72,"type":39},"2025-09-25",{"date":74,"type":21},"2025-09-20",{"date":76,"type":21},"2026-01-31",{"name":78,"class":46},"University of Thessaly",{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":87,"minAge":88,"maxAge":56,"enrollmentInfo":89,"targetDuration":4,"studyType":22,"phases":91,"briefSummary":92,"conditions":93,"keywords":96,"overallStatus":100,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":47},"100580824","the-effect-of-distraction-techniques-used-in-intramuscular-im-injections-on-pain-in-adolescents-presenting-to-the-emergency-department-with-dysmenorrhea-a-randomized-controlled-study-100580824","NCT06842329","The Effect of Distraction Techniques Used in Intramuscular (IM) Injections on Pain in Adolescents Presenting to the Emergency Department With Dysmenorrhea: A Randomized Controlled Study","\"The Effectiveness of Helfer Skin Tap Technique and ShotBlocker in Reducing Pain Severity During Intramuscular Injections in Adolescent Dysmenorrhea: A Randomized Controlled Trial\"","\"HSTT-SB Dysme","nclusion Criteria:\n\n* Adolescents aged 12-18 years.\n* Experience of dysmenorrhea (menstrual pain) during at least one menstrual cycle.\n* Adolescents presenting to the emergency department with dysmenorrhea.\n* Written informed consent from participants or their legal guardians.\n\nExclusion Criteria:\n\n* Individuals with severe cardiovascular, neurological, or other serious medical conditions.\n* Pregnant individuals.\n* Individuals undergoing regular hormonal therapy or using birth control methods.\n* Individuals with significant psychological or physiological conditions related to pain sensitivity (e.g., hyperalgesia).\n* Individuals receiving other pharmacological treatments or pain management medications during the study.","FEMALE","12 Years",{"count":90,"type":21},90,[24],"Brief Summary:\n\nThis study investigates the effectiveness of non-pharmacological techniques for managing dysmenorrhea (menstrual pain) in adolescents. The study focuses on methods such as Helfer Skin Tap Technique (HSTT) and ShotBlocker, which aim to reduce pain without medication. The goal is to determine how these techniques can help adolescents manage their pain more effectively.\n\nThe study targets adolescents aged 12-18 who experience menstrual pain. Participants will be monitored over several months to assess the impact of these techniques on their pain levels, emotional well-being, and daily activities.\n\nParticipation in the study poses minimal risks. However, the effectiveness of these pain management techniques may vary from person to person. By the end of the study, the aim is to improve pain management strategies for adolescents and gain a better understanding of the effectiveness of non-pharmacological treatments for dysmenorrhea.",[94,95,27],"Dysmenorrhea","Pain",[97,98,99],"helfer skin tap","shotblocker","pain management","RECRUITING","2025-02-21",{"date":103,"type":39},"2025-02-24",{"date":105,"type":39},"2024-10-01",{"date":107,"type":21},"2025-04-01",{"name":109,"class":46},"Duygu MEZDE"]