[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Oslo Metropolitan University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":144},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,46,71,98,124],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100530635","positive-feeding-of-the-preterm-infant-100530635",false,"NCT06189352","Positive Feeding of the Preterm Infant","Positive Feeding of the Preterm Infant - a Feasibility Study of a Developmental Supportive Feeding Strategy in the NICU","PoP","Inclusion Criteria:\n\n* gestational age of 28 weeks\n* post menstrual age of 28 weeks after transition from regional hospital\n\nExclusion Criteria:\n\n* diagnoses or malformations that makes eating difficult\n* triplets or more\n* parents not speaking\u002Funderstanding Norwegian or English\n* parents with challenges or special needs for follow up",true,"ALL",{"count":20,"type":21},15,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this feasibility study is to assess the feasibility to implement a feeding strategy for preterm infants.\n\nThe main questions it aims to answer are:\n\n* Is it feasible to implement the PoP-intervention in a level 3a category Neonatal intensive care unit?\n* Is the PoP-intervention acceptable for parents of preterm infants and health care personnel working in Neonatal intensive care unit?\n\nParents of preterm infants and health care personnel will be asked to follow a protocol of a feeding strategy based on the preterm infants development and cues throughout the NICU-stay.",[27,28,29,30,31,32],"Preterm Infant","Breast Feeding","Bottle Feeding","Enteral Feeding","Cue Based Feeding","Develomentally Supportive Care","RECRUITING","2025-08-05",{"date":36,"type":37},"2025-08-11","ACTUAL",{"date":39,"type":37},"2024-10-14",{"date":41,"type":21},"2026-05",{"name":43,"class":44},"Oslo Metropolitan University","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":17,"sex":54,"minAge":55,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":22,"phases":58,"briefSummary":59,"conditions":60,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":65,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":5},"100508069","the-mother-in-norway-study-100508069","NCT05895604","The Mother in Norway Study","The Mother in Norway Study - A Randomised Trial of Nurse-Family Partnership (NFP)","MiNS","Inclusion Criteria: Female; No previous live births; Currently pregnant; Gestation period less than 28 weeks (i.e., less than or equal to 27 weeks, 6 days) at time of recruitment; Live within an area serviced by a NFP Implementing Agency; Not currently enrolled in the study; professionals are concerned about the pregnancy \u002F impending parenthood\n\nExclusion Criteria: Women who have had a previous live birth; Women who are not currently pregnant; Women who are past their 28th week of gestation (i.e., greater than or equal to 28 weeks, 0 days) at time of recruitment; Women who live outside of an area serviced by a NFP Implementing Agency; Women who are currently enrolled in the study; professionals are not concerned about the pregnancy \u002F impending parenthood","FEMALE","16 Years",{"count":57,"type":21},700,[24],"The Norwegian government is implementing the Nurse Family Partnership program (NFP) to combat child abuse and social inequality. This study will examine NFP with an individually randomized controlled parallel-group trial. The study will enroll 700 mothers over three years, with half receiving NFP services and the other half receiving standard care. The primary outcome is violence towards mothers and their children, assessed through questionnaires and observation tests. The study will also evaluate the program's effects on various health-related outcomes using administrative data. Cost-effectiveness analyses will be conducted to compare NFP to existing services and improve its delivery efficiency.",[61,62,63,64],"Maternal Behavior","Injuries","Violence","Mental Health Wellness",{"date":36,"type":37},{"date":67,"type":37},"2023-06-01",{"date":69,"type":21},"2042-12-31",{"name":43,"class":44},{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":4,"eligibilityCriteria":77,"healthyVolunteers":11,"sex":18,"minAge":78,"maxAge":4,"enrollmentInfo":79,"targetDuration":4,"studyType":22,"phases":81,"briefSummary":82,"conditions":83,"keywords":85,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":45},"100553203","treatment-of-phantom-limb-pain-by-intensive-visual-simulation-therapy-100553203","NCT06483035","Treatment of Phantom Limb Pain by Intensive Visual Simulation Therapy","Intensive Visual Simulation as Treatment for Chronic Phantom Limb Pain in Persons With Upper or Lower Limb Amputation - A Randomized Controlled Trial","Inclusion Criteria:\n\n* Unilateral or bilateral lower limb\u002Fupper limb amputees\n* Adults \\> 18 years of age, no age limit\n* A minimum of 12 months since amputation\n* Chronic PLP: \\> 6 months\n* PLP intensity: \\> 3 on the 0-10 VAS scale\n* Analgesic treatments must have been stable for the previous month\n* Stable prosthetic situation (ie, satisfaction with the fitting of the prosthesis) or being a non-user.\n* Adequate Norwegian language skills\n\nExclusion Criteria:\n\n* Significant visual impairment \u002F blind\n* Unable to follow instructions, i.e significant cognitive impairment.","18 Years",{"count":80,"type":21},38,[24],"Phantom limb pain (PLP) is reported by as much as 80 % of patients following an amputation. There is increasing knowledge of the relation between PLP and maladaptive changes in brain cortical regions. Research has shown that the sight of an \"intact arm\" moving in a mirror may reverse maladaptions (Mirror-therapy, MT) and reduce PLP.\n\nThe current project will implement a digital and modernized version of MT, i.e. Intensive Visual Simulation Therapy (IVS-T). Pilot studies have shown promising results on pain reduction in people with phantom limb pain when using IVS-T. However, there is a lack of RCT studies on this patient population.\n\nThis study is a 2-arm randomized controlled trial (RCT) investigating the effectiveness of IVS-T compared with usual care in person with unilateral upper- or lower limb amputation with chronic phantom limb pain.\n\nThe primary aim of the study is to investigate if IVS treatment is superior to usual care in reducing phantom limb pain intensity after 2 months of treatment in unilateral amputees with moderate to severe PLP.\n\nThe study will furthermore explore quality of life, analgesic consumption, phantom pain characteristics, mobility, and disability. In addition, the study utilizes brain imagery during treatments to investigate neural plasticity and the association between PLP and maladaptive cortical changes.",[84],"Phantom Limb Pain",[86,87,88,89],"Amputation","Chronic pain","Intensive Visual Stimulation","RCT","2025-03-18",{"date":92,"type":37},"2025-03-21",{"date":94,"type":37},"2024-09-05",{"date":96,"type":21},"2026-10",{"name":43,"class":44},{"id":99,"slug":100,"hasResults":11,"nctId":101,"briefTitle":102,"officialTitle":102,"acronym":4,"eligibilityCriteria":103,"healthyVolunteers":17,"sex":18,"minAge":104,"maxAge":105,"enrollmentInfo":106,"targetDuration":4,"studyType":22,"phases":108,"briefSummary":109,"conditions":110,"keywords":112,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":117,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":45},"100560523","support-groups---a-model-for-social-inclusion-and-reduction-of-bullying-in-school-100560523","NCT06578260","Support Groups - a Model for Social Inclusion and Reduction of Bullying in School","Inclusion Criteria:\n\n* Primary Schools with more than 200 students\n* Public Health Nurse employed in a 50% position or more\n\nExclusion Criteria:\n\n* Primary Schools with less than 200 students","10 Years","12 Years",{"count":107,"type":21},1586,[24],"Study Title: Support Groups - a model for social inclusion and reduction of bullying in school Study Design: Cluster Randomized Controlled trial (CRCT) Objective: To investigate the effectiveness of a support group intervention using a solution-focused approach among school children in 5th-7th grade in southeastern Norway Intervention: Peer support groups with a solution-focused approach Study Population: School Children",[111],"Bullying",[113,114,115],"Supportgroups","schoolchildren","solution-focused-approach","2024-08-27",{"date":118,"type":37},"2024-08-29",{"date":120,"type":21},"2024-11-01",{"date":122,"type":21},"2028-08-01",{"name":43,"class":44},{"id":125,"slug":126,"hasResults":11,"nctId":127,"briefTitle":128,"officialTitle":128,"acronym":4,"eligibilityCriteria":129,"healthyVolunteers":11,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":130,"targetDuration":4,"studyType":132,"phases":4,"briefSummary":133,"conditions":134,"keywords":4,"overallStatus":136,"whyStopped":4,"lastUpdateSubmitDate":137,"lastUpdatePostDateStruct":138,"startDateStruct":140,"completionDateStruct":141,"leadSponsor":143,"locationsCount":4},"100499520","compressed---a-longitudinal-study-of-compressed-work-schedules-within-the-health-care-and-welfare-services-100499520","NCT05784324","COMPRESSED - A Longitudinal Study of Compressed Work Schedules Within the Health, Care and Welfare Services","Inclusion Criteria:\n\n* Employed within the municipal health, care and welfare services.\n\nExclusion Criteria:\n\n\\-",{"count":131,"type":21},700000,"OBSERVATIONAL","The aim of COMPRESSED is to investigate the potential consequences of a compressed work schedule within the municipal health, care and welfare services.",[135],"The Focus of the Study is Shift Work","NOT_YET_RECRUITING","2023-03-22",{"date":139,"type":37},"2023-03-24",{"date":67,"type":21},{"date":142,"type":21},"2027-12-12",{"name":43,"class":44},""]