[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hrqol-health-related-quality-of-life\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hrqol-health-related-quality-of-life":34},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,56,115],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":36,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":44,"lastUpdatePostDateStruct":45,"startDateStruct":48,"completionDateStruct":50,"leadSponsor":52,"locationsCount":55},"100613601","assess-the-efficacy-of-tailored-patient-information-and-voluntary-patient-managed-outpatient-digital-follow-up-i-pod-as-an-adjunct-to-standard-treatment-according-to-national-guidelines-in-the-national-trauma-plan-among-adult-trauma-patients-in-norway-100613601",false,"NCT07268716","Assess the Efficacy of Tailored Patient Information and Voluntary Patient-managed Outpatient Digital Follow-up (I-POD) as an Adjunct to Standard Treatment According to National Guidelines in the National Trauma Plan Among Adult Trauma Patients in Norway.","A Randomized Controlled Clinical Trial to Assess the Efficacy of Tailored Patient Information and Voluntary Patient-Managed Outpatient Digital Follow-Up as an Adjunct to Standard Treatment According to National Guidelines in Adult Trauma Patients in Norway (The POSTRAUMA Trial).","POSTRAUMA","Inclusion Criteria:\n\n* 16 years or older\n* Fulfils the national criteria for TTA and admitted to HUS following trauma\n* Included in NTR database\n* Able to give informed consent\n\nExclusion Criteria:\n\n* 15 years or younger\n* Not included in NTR database\n* Deceased before discharge from the hospital.\n* Not able to give informed consent\n* Insufficient command of the Norwegian language\n* Foreign tourists or nationals\n* Suicide attempt or serious self-inflicted trauma\n* Serious psychiatric disorders or serious ongoing substance abuse","ALL","16 Years",{"count":20,"type":21},256,"ESTIMATED","INTERVENTIONAL",[24],"NA","The POSTRAUMA trial is a clinical trial at The Regional trauma centre of Western Norway, Haukeland University Hospital.\n\nTrauma is the leading cause of death worldwide in patients aged 1-45 years. In Norway, approximately 10,000 patients are admitted to hospital annually due to trauma, with 66% being male. The mean age is 43 years for male and 48 years for female, indicating a relatively young patient population.\n\nWhile mortality rates are decreasing, a significant proportion of trauma survivors experience long-term disabilities, reduced quality of life, and difficulties in returning to work. These consequences impose substantial burdens on individuals, families, and society. Considering these issues, a shift in focus is needed-from survival alone to long-term functional recovery and quality of life after trauma.\n\nSevere trauma often requires long-term follow-up, both physically and psychosocially. Traditional follow-up can be fragmented and not tailored to individual needs. Digital patient monitoring and tailored information have the potential to improve patient pathways, but knowledge about how these are experienced by patients is limited.\n\nThe goal is to find out if Norwegian trauma patients who receive tailored patient information and patient-managed outpatient digital follow-up, in addition to standard treatment have:\n\n* Less disability\n* Return more often to work\n* Improved quality of life\n\nThe study population are Norwegian trauma patients, 16 years or older at date of inclusion, who are admitted to Haukeland University hospital (HUS) following trauma with trauma team activation. 256 patients will be included in this trial.\n\nParticipants will:\n\n* Answer a questionnaire at inclusion, one month, 6 months and 12 months.\n* Participants in the intervention group will be invited to digital outpatient follow up one month after the accident.\n* Some participants will be interviewed about how they experienced their trauma follow up.",[27,28,29,30,31,32,33,34,35],"Trauma Centers","Trauma Patients","Trauma (Including Fractures)","Trauma Injury","Rehabilitation After Neurological or Orthopaedic Injuries","Rehabilitation","Return to Work","HRQOL (Health Related Quality Of Life)","EQ5D5L-VAS",[37,38,39,40,41,42],"multitrauma","trauma","rehabilitation","return to work","HRQOL","EQ5D","NOT_YET_RECRUITING","2025-12-16",{"date":46,"type":47},"2025-12-22","ACTUAL",{"date":49,"type":21},"2026-03-02",{"date":51,"type":21},"2029-12-31",{"name":53,"class":54},"Haukeland University Hospital","OTHER",1,{"id":57,"slug":58,"hasResults":11,"nctId":59,"briefTitle":60,"officialTitle":61,"acronym":62,"eligibilityCriteria":63,"healthyVolunteers":64,"sex":17,"minAge":65,"maxAge":66,"enrollmentInfo":67,"targetDuration":4,"studyType":69,"phases":4,"briefSummary":70,"conditions":71,"keywords":74,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":109,"completionDateStruct":111,"leadSponsor":113,"locationsCount":55},"100603274","long-term-burden-of-bpd-and-health-related-quality-of-life-bronq-family-100603274","NCT07134387","Long-Term Burden of BPD and Health-Related Quality of Life (BronQ Family)","BronQ Family: Assessing the Long-term Impact of Bronchopulmonary Dysplasia (BPD) on Affected Families' Health-related Quality of Life","BronQ Family","Inclusion Criteria:\n\nBPD-group:\n\n* Being a parent or primary caregiver of a child until the age of 18 years (0 to under 18 years),\n\n  * who was born preterm (before 37 weeks of gestation),\n  * who has been discharged from their initial hospital stay after birth,\n  * who suffered from BPD in the newborn period and\n  * who was born or is currently living in the following countries: France, Germany, Italy, the Netherlands, Spain, the United Kingdom (including Northern Ireland) and the United States\n* providing sufficient proficiency in one of the languages of the questionnaire\n\nControl group:\n\n* Being a parent or primary caregiver of a child until the age of 18 years (0 to under 18 years),\n\n  * who was born preterm (before 37 weeks of gestation),\n  * who has been discharged from their initial hospital stay after birth,\n  * who did not suffer from BPD in the newborn period and\n  * who was born or is currently living in the following countries: France, Germany, Italy, the Netherlands, Spain, the United Kingdom (including Northern Ireland) and the United States\n* providing sufficient proficiency in one of the languages of the questionnaire\n\nExclusion Criteria:\n\nBPD-group:\n\n* Other family members than parents\u002Fprimary caregivers\n* Parents or primary caregivers\n\n  * of a child older\u002Fequal than 18 years of age\n  * of a child with BPD who has not been discharged yet\n  * of a child without a BPD in the newborn period\n  * with insufficient proficiency in one of the languages available in the questionnaire\n\nControl group:\n\n* Other family members than parents\u002Fprimary caregivers\n* Parents or primary caregivers\n\n  * of children older\u002Fequal than 18 years of age\n  * of a child born term\n  * of a child without BPD who has not been discharged yet\n  * with insufficient proficiency in one of the languages available in the questionnaire",true,"0 Years","18 Years",{"count":68,"type":21},480,"OBSERVATIONAL","The objective of this study is to examine the long-term impact of having a child with Bronchopulmonary Dysplasia (BPD) on the parents and caregivers from the time of diagnosis through adulthood. The primary focus will be on parents and caregivers of children until the age of 18 (\\\u003C 18) years who were diagnosed with BPD as newborns. Data will be collected through an online questionnaire in France, Germany, Italy, the Netherlands, Spain, the United Kingdom (including Northern Ireland), and the United States. It will ask about inclusion and exclusion criteria, background information (caregiver, child, and family situation), the child's medical situation, parental health-related quality of life (HRQoL), health literacy, feelings, support structures, and economic burden of the family.",[72,73,34],"Bronchopulmonary Dysplasia (BPD)","Chronic Lung Disease of Newborn",[75,76,77,78,79,80,81,72,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104],"Parental Quality of life","QoL","Health-related quality of life","HRQoL","Caregiver burden","Parental well-being","Family","Chronic Lung Disease (CLD)","Chronic Lung Diseaseof Newborn","Respiratory Morbidity","Long-term outcomes","Parents","Caregivers","Infants","Newborn","Children","Preterm","Prematurity","NICU","Intensive Care","Neonatal","Survey","Questionnaire","Multinational study","retrospective data collection","participatory research","Patient-reported outcomes","PROs","Patient-reported outcome measures","PROMs","RECRUITING","2025-11-18",{"date":108,"type":47},"2025-11-21",{"date":110,"type":47},"2025-09-16",{"date":112,"type":21},"2027-01",{"name":114,"class":54},"Global Foundation for the Care of Newborn Infants",{"id":116,"slug":117,"hasResults":11,"nctId":118,"briefTitle":119,"officialTitle":120,"acronym":4,"eligibilityCriteria":121,"healthyVolunteers":11,"sex":17,"minAge":122,"maxAge":123,"enrollmentInfo":124,"targetDuration":4,"studyType":69,"phases":4,"briefSummary":126,"conditions":127,"keywords":129,"overallStatus":105,"whyStopped":4,"lastUpdateSubmitDate":132,"lastUpdatePostDateStruct":133,"startDateStruct":135,"completionDateStruct":137,"leadSponsor":139,"locationsCount":55},"100585748","health-related-quality-of-life-in-children-and-adolescents-with-clubfoot-100585748","NCT06906406","Health-Related Quality of Life in Children and Adolescents With Clubfoot","Health-Related Quality of Life in Children and Adolescents With Clubfoot. A Prospective Observational Study","Inclusion Criteria:\n\n* Children aged 2 to 15 years diagnosed with congenital clubfoot.\n* Undergoing treatment or follow-up at Drammen Hospital.\n* Both unilateral and bilateral cases included.\n* Written informed consent from parents or legal guardians.\n\nExclusion Criteria:\n\n* Concurrent severe medical or psychological conditions affecting outcomes.\n* Lack of written informed consent.\n* Incomplete or missing data for PedsQL or PBS assessments.","2 Years","15 Years",{"count":125,"type":21},30,"This prospective cohort study aims to evaluate the health-related quality of life (HRQoL) in children aged 2 to 15 years with congenital clubfoot, treated primarily according to the Ponseti method. The study will assess HRQoL using the Pediatric Quality of Life Inventory (PedsQL 4.0) and clinical outcomes using the PBS Clubfoot Score (PBS). Participants will be followed for 2 and 5 years to evaluate changes in HRQoL and clinical function. The primary objective is to understand the long-term impact of clubfoot and its treatment on patients' physical, emotional, and social well-being.",[128,90,34],"Clubfoot",[78,130,90,128,131],"PedsQL","Ponseti","2025-03-28",{"date":134,"type":47},"2025-04-02",{"date":136,"type":47},"2025-01-01",{"date":138,"type":21},"2030-12-31",{"name":140,"class":54},"Vestre Viken Hospital Trust"]