[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100635371":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":24,"locations":30,"responsibleParty":44,"collaborators":18,"id":48,"slug":18,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":18,"eligibilityCriteria":52,"healthyVolunteers":49,"sex":53,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":18,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":70,"overallStatus":75,"whyStopped":18,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":85},{"fullName":5,"class":6},"Gazi University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Application group","EXPERIMENTAL","After the purpose of the study and the method of application are explained to the intensive care patients, the \"Patient Identifier Information Form\", \"Cancer Fatigue Scale\", \"Functional Assessment of Cancer Therapy-General Scale (FACT-G)\", \"Hospital Anxiety and Depression Scale (HADS)\", and \"Nurse Presence Scale (PONS)\" will be applied. A total of 2 week (3 sessions per week) of art-based intervention will be applied . The measurements will be repeated afterwards.",[13],"Other: art-based intervention",{"label":15,"type":16,"description":17,"interventionNames":18},"Control Group","NO_INTERVENTION","No application will be made to the control group.",null,[20],{"type":6,"name":21,"description":22,"armGroupLabels":23,"otherNames":18},"art-based intervention","The Art-Based Intervention program will be implemented in 3 sessions per week, for a total of 6 sessions. Before starting the Art-Based Intervention program, the researcher will provide information about the purpose of the activity and the tools to be used. Each session will have a theme, and the session will be conducted according to the instructions given to the patient within the framework of this theme. Before each session, the theme specific to that day will be explained to the patients. Sessions will last approximately 45 minutes.",[9],[25],{"name":26,"role":27,"phone":28,"phoneExt":18,"email":29},"Ozlem Canbolat","CONTACT","+90 312 216 26 86","ozlemcanbolat@gazi.edu.tr",[31],{"facility":5,"status":18,"city":32,"state":33,"zip":34,"country":35,"countryCode":18,"cosmosGeoPoint":36,"geoPoint":41,"contacts":42},"Ankara","Çankaya","06560","Turkey (Türkiye)",{"type":37,"coordinates":38},"Point",[39,40],32.85427,39.91987,{"lat":40,"lon":39},[43],{"name":26,"role":27,"phone":28,"phoneExt":18,"email":29},{"type":45,"investigatorFullName":46,"investigatorTitle":47,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","Özlem Canbolat","Associate Professor","100635371",false,"NCT07551817","The Effect of Art-Based Intervention on Fatigue, Anxiety, Perception of Nurse Presence, and Quality of Life in Patients With Hematological Cancers","Inclusion Criteria:\n\n* Being between 18 and 65 years of age\n* Speaking and understanding Turkish\n* Being literate\n* Having a diagnosis of hematological cancer,\n* Receiving chemotherapy in an inpatient ward,\n* Not having a psychiatric diagnosis,\n* Having an ECOG score of 1 or 2,\n\nExclusion Criteria:\n\n* Having vision loss and hearing loss,\n* Having an ECOG score of 3 or 4\n* Patients who wanted to leave the study\n* Failure to attend at least two sessions of art therapy.","ALL","18 Years","65 Years",{"count":57,"type":58},52,"ESTIMATED","INTERVENTIONAL",[61],"NA","This study will be conducted in a randomized controlled experimental design to examine The effect of art-based intervention on fatigue, anxiety, perception of nurse presence, and quality of life in patients with hematological cancer. The study will be conducted with 52 patients (26 intervention, 26 control groups) treated in the Hematology department of a training and research hospital between May 2025 and October 2026. Art-based intervention will be applied to the intervention group for 2 week (3 sessions per week), No application will be made to the control group. The data collection tools in the study are the Patient Identifier Information Form, Cancer Fatigue Scale, Functional Assessment of Cancer Therapy-General Scale (FACT-G), Hospital Anxiety and Depression Scale (HADS), and Nurse Presence Scale (PONS).",[64,65,66,67,68,69],"Art-based Intervention","Hematological Cancer","Nurse Presence","Quality of Life","Fatigue","Anxiety",[71,72,73,74,68,69],"Art-based intervention","Hematological cancer","Nurse presence","Quality of life","NOT_YET_RECRUITING","2026-04-22",{"date":78,"type":79},"2026-04-27","ACTUAL",{"date":81,"type":58},"2026-05-01",{"date":83,"type":58},"2026-12-31",{"name":5,"class":6},1]