[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100563767":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":18,"locations":27,"responsibleParty":50,"collaborators":18,"id":53,"slug":54,"hasResults":55,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":18,"eligibilityCriteria":59,"healthyVolunteers":55,"sex":60,"minAge":61,"maxAge":62,"enrollmentInfo":63,"targetDuration":18,"studyType":66,"phases":67,"briefSummary":69,"conditions":70,"keywords":74,"overallStatus":77,"whyStopped":18,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":87},{"fullName":5,"class":6},"Pakistan Institute of Medical Sciences","OTHER_GOV",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Interventional Group","EXPERIMENTAL","The Intervention or CBT group included 40 children aged 8-16 years with malignancies recieving chemotherapy. They will recieve weekly five sessions of CBT (30-35 minutes per session)",[13],"Behavioral: Interventiion or CBT Group",{"label":15,"type":16,"description":17,"interventionNames":18},"Control or Usual Care Group","NO_INTERVENTION","The Control or No Intervention Group also known as Comparision Group or Usual Group will recieve the standard care or usual care for their condition. It will serve as a baseline for the CBT or Intervention Group.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"BEHAVIORAL","Interventiion or CBT Group","This RCT aims to evaluate the effect of Cognitive Behavioral Therapy (CBT) compared to usual care (UC) in pediatric oncology patients. We hypothesize that those receiving CBT will report lower depression and anxiety and improved QoL six months post-enrollment.",[9],[26],"Cognitive or Pschological Intervention",[28],{"facility":29,"status":18,"city":30,"state":18,"zip":31,"country":32,"countryCode":33,"cosmosGeoPoint":34,"geoPoint":39,"contacts":40},"Muhammad Wasim Khan","Islamabad","44000","Pakistan","PK",{"type":35,"coordinates":36},"Point",[37,38],73.04329,33.72148,{"lat":38,"lon":37},[41,46],{"name":42,"role":43,"phone":44,"phoneExt":18,"email":45},"Muhammad Wasim Khan, MBBS, FCPS","CONTACT","03334411620","mail4wasimkhan@gmail.com",{"name":47,"role":43,"phone":48,"phoneExt":18,"email":49},"Nuzhat Yasmeen, MBBS, FCPS, DPH, PhD","03332135791","drnuzhatyasmeen@yahoo.com",{"type":51,"investigatorFullName":52,"investigatorTitle":52,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","Dr. Muhammad Wasim Khan","100563767","efficacy-of-psychological-intervention-for-children-with-cancer-100563767",false,"NCT06620445","Efficacy of Psychological Intervention for Children With Cancer","Efficacy of Psychological Intervention for Children With Cancer: A Randomized Controlled Trail","Eligibility Criteria:\n\nInclusion Criteria:\n\n1. Children aged 16-18 years\n2. Diagnosed with malignancy\n3. Recieving chemotherapy at the Pediatric Oncology Department of PIMS Islamabad\n4. Able to understand and participate in CBT sessions\n5. Parent\u002FCaregiver consent and child assent\n\nExlusion Criteria:\n\n1. Children with severe cognitive impairment or intellectual disability\n2. Children with a comorbid medical conditions\n3. Children whose parents or caregivers are unable to provide consent","ALL","8 Years","16 Years",{"count":64,"type":65},80,"ESTIMATED","INTERVENTIONAL",[68],"NA","The study will be conductued at the Pediatric Oncology Department of the Children's Hospital, PIMS Islamabad, over the peroid of six months. This single-blinded, two-arm RCT study will involve 80 children aged 8 to 16 years with maligancies recieving chemotherapy. Participants will be randomly allocated to either interventional or CBT group which will recieve weekly five sessions of Cognitive Behaviour Therapy (CBT) or the control group, which will recieve the usual care. CBT session will be contducted by Clinical Psychologist will last 30-35 minutes. Outcomes will be measured at Baseine and one month post intervention using Revised Child Anxiety and Depression Scale (RCADS) and Pediatric Quality of Life Generic Core Score 4.0.",[71,72,73],"Clinical Depression","Clinical Anxiety","Quality of Life",[75,76],"Psychological Intervention","Pediatric Cancer","NOT_YET_RECRUITING","2024-09-26",{"date":80,"type":81},"2024-10-01","ACTUAL",{"date":83,"type":65},"2024-10-10",{"date":85,"type":65},"2025-06-30",{"name":5,"class":6},1]