[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Joint Authority for Päijät-Häme Social and Health Care\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":158},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,40,70,97,135],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100438993","day-case-colectomy-optimizing-short-stay-surgery-100438993",false,"NCT04996511","Day Case Colectomy: Optimizing Short Stay-surgery.","Inclusion Criteria:\n\n• Colorectal resection for any pathology\n\nExclusion Criteria:\n\n• Arrhytmias likely to cause problems with HRV measurements","ALL","18 Years","100 Years",{"count":19,"type":20},30,"ESTIMATED","INTERVENTIONAL",[23],"NA","HRV measurement of patients recovering from laparoscopic colorectal resection for any pathology.",[26],"Monitoring, Physiologic","RECRUITING","2026-04-21",{"date":30,"type":31},"2026-04-22","ACTUAL",{"date":33,"type":31},"2020-01-01",{"date":35,"type":20},"2027-12-31",{"name":37,"class":38},"Joint Authority for Päijät-Häme Social and Health Care","OTHER",1,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":47,"targetDuration":4,"studyType":21,"phases":49,"briefSummary":50,"conditions":51,"keywords":57,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":69,"locationsCount":39},"100564743","stroke-rehabilitation-utilizing-therapeutical-methods-designed-for-nature-environments-100564743","NCT06633146","Stroke Rehabilitation Utilizing Therapeutical Methods Designed for Nature Environments","Outpatient Stroke Rehabilitation Supported by Nature Interventions","Inclusion Criteria:\n\n* Acute stroke\n\nExclusion Criteria:\n\n* Traumatic intracranial bleeding without stroke\n* A malign, aggressive disease\n* Severe aphasia or incapable of independent decision making",{"count":48,"type":20},40,[23],"Outpatient participants with a recent stroke diagnoses receive complimentary rehabilitation. The nature interventions include ergo- and physiotherapeutic and neurocognitive tasks with the support of an psychotherapeutic frame designed to be performed in a nature environment.",[52,53,54,55,56],"Stroke","Stress, Psychological","Post Traumatic Stress Disorder","Depression, Anxiety","Loneliness",[58,59,60,61,62],"stroke","rehabilitation","social support","cognitive functions","activity","2025-02-25",{"date":65,"type":31},"2025-02-28",{"date":67,"type":31},"2024-06-01",{"date":35,"type":20},{"name":37,"class":38},{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":77,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":78,"targetDuration":4,"studyType":21,"phases":80,"briefSummary":81,"conditions":82,"keywords":84,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":92,"completionDateStruct":94,"leadSponsor":96,"locationsCount":39},"100508294","nature-based-therapies-in-stroke-rehabilitation-100508294","NCT05898542","Nature-based Therapies in Stroke Rehabilitation","Nature-based Therapies Supporting Conventional Therapies in Promoting Stroke Rehabilitation: a Randomised Controlled Pilot Study.","Inclusion Criteria:\n\n* Acute\u002FSubacute stroke\n* Rehabilitation ward patient\n\nExclusion Criteria:\n\n* Incapable of independent decision making\n* Traumatic bleeding in brain tissue\n* Severe aphasia\n* Severe, malign ongoing disease",true,{"count":79,"type":20},60,[23],"Stroke rehabilitation patients are subjected to additional nature-based therapies during a rehabilitation ward period.",[83,52],"Rehabilitation",[59,58,85,86,87,88],"nature-based","therapy","microbiome","gut-brain axis","2024-07-01",{"date":91,"type":31},"2024-07-03",{"date":93,"type":31},"2023-05-31",{"date":95,"type":20},"2026-12-31",{"name":37,"class":38},{"id":98,"slug":99,"hasResults":11,"nctId":100,"briefTitle":101,"officialTitle":101,"acronym":4,"eligibilityCriteria":102,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":103,"enrollmentInfo":104,"targetDuration":4,"studyType":21,"phases":106,"briefSummary":107,"conditions":108,"keywords":113,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":39},"100374148","health-psychological-group-rehabilitation-for-patients-with-chronic-fatigue-syndrome-mecfs-100374148","NCT04151693","Health Psychological Group Rehabilitation for Patients With Chronic Fatigue Syndrome (ME\u002FCFS)","Inclusion Criteria:\n\n* Clinical diagnosis of Chronic fatigue syndrome, G 93.3\n* Must be able to sit two hours and do homework tasks\n* Must be motivated to co-operate with other patients\n* Goal oritentation\n* Have an interest to learn health psychological approach and willingness to participate rehabilitation\n\nExclusion Criteria (diseases without treatment\u002F acute phase):\n\n* hypothyroidism\n* sleep apnea or narcolepsy\n* major depressive disorders, bipolar affective disorders, schizophrenia\n* eating disorders\n* cancer\n* autoimmune disease\n* hormonal disorders\n* subacute infections\n* obesity\n* alcohol or substance abuse\n* vitamin D deficiency","65 Years",{"count":105,"type":20},80,[23],"Chronic fatigue syndrome (ME\u002FCFS) is a severe medical condition. It is characterized by long term fatique and other persisted symptoms, such as a cognitive disabilities and orthostatic intolerance. Symptoms limit a persons ability to carry out ordinary daily activities. In ICD- 10, disease is known as G93.3, postviral fatigue syndrome.\n\nThe purpose of this research (doctoral study) is to produce a health psychological group intervention for patients with ME\u002FCFS.\n\nResearch protocol: 70-80 patients with diagnosis G 93.3. Psychological and psychiatric evaluation for patients (SCID I and parts from SCID II). Depression diagnosis is allowed (on remission). Medication for depression is also allowed. Measurements for ortostatic intolerance (Somnotouch nimbTM) and laboratory measurements: complete blood count, CRP, alkaline phosphatase, GT, ALAT, CK, bilirubin, kidney and thyroid (TSH, T4V) function tests, serum ferritin, glucose, electrolytes and daily urine sodium excretion.\n\nAutonomic nervous system ganglio antibodies: Anti-AT1R- Antibodies, Anti- ETAR- Antibodies, anti alpha-1 adrenergic Receptor Antibodies, anti alpha 2 adrenergic Receptor Antibodies, anti beta-1 adrenergic Receptor Antibodies, anti beta-2-adrenergic Receptor Antibodies, anti- Muscarinic Cholinergic Receptor 1 (M1)- Antibodies, anti- Muscarinic Cholinergic Receptor 2 (M2)- Antibodies, anti- Muscarinic Cholinergic Receptor 3 (M3)- Antibodies, anti- Muscarinic Cholinergic Receptor 4 (M4)- Antibodies, anti- Muscarinic Cholinergic Receptor 5 (M5)- Antibodies.",[109,110,111,112],"Psychological Adaptation","Cognitive Change","Adaptive Behavior","Functioning",[114,115,116,117,118,119,120,121,122,123,124,125,126],"Psychological intervention","Cognitive Behavioral Therapy (CBT)","Accept and Commitment Therapy (ACT)","Cognitive functioning","Fatigue","Autonomic nervous system","Autonomic nervous system ganglio antibodies","Deep breathing","Relaxation","Health care system","Agency","Health psychology","Pacing","2024-04-02",{"date":129,"type":31},"2024-04-03",{"date":131,"type":31},"2019-11-30",{"date":133,"type":20},"2028-05-31",{"name":37,"class":38},{"id":136,"slug":137,"hasResults":11,"nctId":138,"briefTitle":139,"officialTitle":140,"acronym":141,"eligibilityCriteria":142,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":143,"enrollmentInfo":144,"targetDuration":4,"studyType":146,"phases":4,"briefSummary":147,"conditions":148,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":150,"lastUpdatePostDateStruct":151,"startDateStruct":153,"completionDateStruct":155,"leadSponsor":157,"locationsCount":39},"100341941","the-finnish-faecal-microbiota-transplantation-study-finfmt-100341941","NCT03732131","The Finnish Faecal Microbiota Transplantation Study (FINFMT)","Long Term Safety and Efficacy of Faecal Microbiota Transplantation: a Nationwide Obeservational Study","FINFMT","Inclusion Criteria:\n\n* \\> 18 years age\n* receiving FMT for rCDI or any other madical condition\n* written consent\n* Not included in other FMT trials\n\nExclusion Criteria:\n\n* Unable to provide written consent\n* \\\u003C 18 years age\n* Included in other FMT-trial","120 Years",{"count":145,"type":20},200,"OBSERVATIONAL","The objective of the study is to follow up the long term effects of faecal microbiota tranplantation (FMT). All the over 18 years old patients receiving FMT and not included in other trials meet inclusion criteria to this study. Patients will be asked for a written consent. The outcome and possible side effects of the FMT will be followed by blood and feces samples for one year and with questionaires up to ten years after the FMT.",[149],"Faecal Microbiota Transplantation","2020-02-13",{"date":152,"type":31},"2020-02-17",{"date":154,"type":31},"2018-10-18",{"date":156,"type":20},"2029-01-15",{"name":37,"class":38},""]