[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"blood-sampling\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:blood-sampling":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,53],{"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":33,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100649221","two-different-therapeutic-interventions-applied-during-blood-sampling-in-children-100649221",false,"NCT07731347","Two Different Therapeutic Interventions Applied During Blood Sampling in Children","The Effect of Two Different Therapeutic Interventions on Pain, Anxiety and Fear During Venipuncture in Children","Inclusion Criteria:\n\n* Being between 5 and 7 years old,\n* Having a scheduled venous blood sampling procedure in the Pediatric Emergency Unit,\n* Having a level of consciousness suitable for communication,\n* The child and their parents agreeing to participate in the study,\n* Being able to communicate in Turkish.\n\nExclusion Criteria:\n\nInability to participate in the application due to visual or hearing problems,\n\n* Inability to administer the scales due to a developmental or neurological disease,\n* Being under the influence of sedative or analgesic medication,\n* Inability to complete the application during the research process,\n* Lack of parental consent.",true,"ALL","5 Years","7 Years",{"count":21,"type":22},105,"ESTIMATED","INTERVENTIONAL",[25],"NA","This research is a three-group, randomized controlled experimental study designed to determine the effect of two different therapeutic interventions applied during blood sampling on pain, anxiety, and fear levels in children aged 5-7 years.\n\nChildren participating in the study will be randomly divided into three groups:\n\n1. Group (Experiment 1): Distraction method using betta fish observation\n2. Group (Experiment 2): Distraction method using hand puppets\n3. Group (Control): Routine clinical practice (without any therapeutic intervention) Before, during, and after blood sampling, children's pain level (FLACC scale), fear level (child fear scale), and anxiety level (child anxiety scale) will be evaluated.",[28,29,30,31,32],"Blood Sampling","Child, Only","Pain","Fear","Nurse's Role",[34,35,36,37,38,39],"Play Therapy","blood sampling","child","pain","fear","nursing","NOT_YET_RECRUITING","2026-07-28",{"date":43,"type":44},"2026-07-29","ACTUAL",{"date":46,"type":22},"2026-08-01",{"date":48,"type":22},"2026-12-01",{"name":50,"class":51},"Igdir University","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":57,"acronym":58,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":17,"minAge":60,"maxAge":4,"enrollmentInfo":61,"targetDuration":4,"studyType":63,"phases":4,"briefSummary":64,"conditions":65,"keywords":69,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":52},"100626411","analysis-of-inflammatory-biomarker-changes-in-dry-blood-spot-versus-venous-blood-samples-100626411","NCT07435285","Analysis of Inflammatory Biomarker Changes in Dry Blood Spot Versus Venous Blood Samples","DBS-VB","Inclusion Criteria:\n\n* Men or women aged ≥18 years, who are planning to receive a seasonal vaccine OR have a scheduled acute stressor\\*.\n\nExclusion Criteria:\n\n* Any infectious symptoms (fever, cough, rhinorrhea, sore throat, diarrhea, loss of smell or taste) within the previous 7 days\n* Any self-reported active\u002Frecent use of cocaine, injection drugs, or amphetamines\n* Acute worsening of a known chronic health condition within the previous 30 days (e.g., of IBD, COPD, asthma, rheumatologic disease)\n* Known severe allergy or intolerance to the planned vaccine\n* Contraindication to the vaccine received, if applicable\n\n  \\*List of possible scheduled acute stressors include:\n* Hard exercise (incl. 10km run or longer, high-intensity interval training, or comparable endurance activity)\n* Social event with moderate alcohol consumption\n* Planned change in medication dose and\u002For frequency of use\n* Onset of menstruation (day 1)\n* Other pre-planned stressors expected to elicit an inflammatory response","18 Years",{"count":62,"type":22},50,"OBSERVATIONAL","The purpose of this study is to see whether dried blood spot (DBS) samples can measure inflammatory biomarkers as accurately as venous blood samples.\n\nInvestigators will be measuring inflammatory biomarkers changes obtained in DBS compared with paired venous blood samples following a controlled physiological stressor (i.e. after a vaccine or other planned event that can cause a temporary rise in inflammation).\n\nThese findings will help understand whether DBS can be a reliable alternative to traditional blood draws in future research and healthcare.",[66,67,28,68],"Inflammation","Inflammation Biomarkers","Dried Blood Spot",[70,35,71,72,73,74],"inflammation","biomarkers","inflammatory biomarkers","dried blood spot","paired sampling","RECRUITING","2026-03-23",{"date":78,"type":44},"2026-03-27",{"date":80,"type":44},"2026-01-15",{"date":82,"type":22},"2026-12",{"name":84,"class":51},"McGill University Health Centre\u002FResearch Institute of the McGill University Health Centre"]