[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Eastern Switzerland University of Applied Sciences\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":150},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,41,71,96,124],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":21,"conditions":22,"keywords":26,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100629604","capturing-parental-wellbeing-in-everyday-life-through-a-mobile-diary-app-100629604",false,"NCT07476833","Capturing Parental Wellbeing in Everyday Life Through a Mobile Diary App","Parental Wellbeing in Everyday Life: Ecological Momentary Assessment Study on the Wellbeing of Parents of Children Aged 0 - 12 in Switzerland","Inclusion Criteria:\n\nParents living in Switzerland\n\n* with at least one child aged between 0 months - 11 years and 11 months\n* German-speaking\n* any form of parenting\n* any relationship status\n* any form of couples or other forms of cohabitation\n* No restrictions regarding nationality, wealth, external childcare, employment (full-time, part-time or homemaker) or similar characteristics.\n\nParticipants must have a smartphone with internet access to participate in the mobile diary study\n\nExclusion Criteria:\n\n* All Children \\> 11 years and 11 months of age\n* Not German speaking\n* Swiss nationality but living abroad\n* No smartphone with internet access","ALL",{"count":18,"type":19},300,"ESTIMATED","OBSERVATIONAL","This observational study investigates the wellbeing of parents in German-speaking Switzerland in everyday contexts using smartphone-based Ecological Momentary Assessment (EMA). Family caregiving can be both rewarding and burdensome, yet little is known about how parental wellbeing fluctuates in daily life and across caregiving situations. The study aims to examine momentary subjective wellbeing, caregiving activities, and contextual factors in natural settings. Participants complete repeated real-time assessments via a digital diary application five times a day over a 14-day study period. The study seeks to characterize within-person variability in parental wellbeing and identify contextual factors associated with positive and negative daily experiences.",[23,24,25],"Wellbeing","Sleep","Support, Family",[27],"Parental Wellbeing","NOT_YET_RECRUITING","2026-03-12",{"date":31,"type":32},"2026-03-17","ACTUAL",{"date":34,"type":19},"2026-03-01",{"date":36,"type":19},"2026-07-31",{"name":38,"class":39},"Eastern Switzerland University of Applied Sciences","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":16,"minAge":47,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":56,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":40},"100575780","hyperoxia-during-outpatient-pulmonary-rehabilitation-in-chronic-lung-disease---does-it-matter-100575780","NCT06776731","Hyperoxia During Outpatient Pulmonary Rehabilitation in Chronic Lung Disease - Does it Matter?","Inclusion Criteria:\n\n* We will include male and female with a confirmed diagnosis of COPD (post-bronchodilator forced expiratory volume in one second (FEV1) \u002F forced vital capacity (FVC) ratio of \\\u003C0.7; a greater than 10 pack-year smoking history)\n* undergoing pulmonary rehabilitation\n* aged ≥ 18 years\n* stable condition \\> 3 weeks (e.g. no exacerbations)\n* resting oxygen saturation (SpO2) ≥ 88%\n* exercise induced hypoxemia defined by a fall in SpO2 by ≥ 4% and\u002F or below 90% during a 6MWT\n* informed consent as documented by signature.\n\nExclusion Criteria:\n\n* Severe daytime resting hypoxemia (SpO2 \\\u003C 88% )\n* long-term oxygen therapy, unstable condition requiring adaptation of pharmacologic and other treatment modalities or requirement of intensive care or relevant severe concomitant disease\n* inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, neurological or orthopedic problems with walking disability or inability to ride a bicycle\n* women who are pregnant or breast feeding; enrolment in another clinical trial with active treatment.","18 Years",{"count":49,"type":19},32,"INTERVENTIONAL",[52],"NA","Chronic obstructive pulmonary disease (COPD) is a global burden. Treatment options have improved in recent years, pulmonary rehabilitation plays a key role. Oxygen therapy is recommended in patients with a low saturation at rest, but no clear guidance is given for patients who desaturate during exercise. The effect of ambulatory oxygen during exercise is not yet completely understood, especially in those patients with exercise-induced desaturation.\n\nAim: Evaluate the effect of supplemental oxygen therapy during a 3-months long ambulatory pulmonary rehabilitation program on exercise endurance. Patients will either receive supplemental oxygen therapy or room air during exercise training.\n\nMethods: A total of 32 patients with a confirmed diagnosis of COPD undergoing pulmonary rehabilitation will be included (male and female : aged ≥ 18 years; stable condition \\> 3 weeks (e.g. no exacerbations); resting oxygen saturation (SpO2) ≥ 88% and exercise induced hypoxemia defined by a fall in SpO2 by ≥ 4% and\u002F or below 90% during a 6-minute walking test). 3-months comprehensive PR for both intervention and control group including: education and awareness, instruction on inhalation therapies, smoking cessation counselling, respiratory and skeletal muscle training in groups, guided walks \u002F cycle ergometer training. The intervention group will be trained using SSOT and the control group will receive sham air (ambient air). Patients and assessors will be blinded. Between group difference in cycling constant work rate exercise test (CWRET) time from baseline to 3 months SSOT (5l\u002Fmin) vs ambient air will be the primary outcome of this study.\n\nData will be summarized by means (SD) and medians (quartiles) for normal and non-normal distributions. Effects of treatment will be evaluated by mean differences with 95% confidence intervals, T-tests or Wilcoxon matched pair tests as appropriate. A p-value threshold of \\\u003C0.05 or a confidence interval not including zero will be considered as statistically significant. Analyses will be performed according to the intention to treat principle.",[55],"Chronic Obstructive Pulmonary Disease (COPD)",[57,58,59,60,61],"COPD","oxygen therapy","pulmonary rehabilitation","hyperoxia","exercise medicine","RECRUITING","2025-08-04",{"date":65,"type":32},"2025-08-07",{"date":67,"type":32},"2025-01-06",{"date":69,"type":19},"2027-08-01",{"name":38,"class":39},{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":4,"eligibilityCriteria":77,"healthyVolunteers":11,"sex":16,"minAge":47,"maxAge":4,"enrollmentInfo":78,"targetDuration":4,"studyType":50,"phases":80,"briefSummary":81,"conditions":82,"keywords":83,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":95},"100597828","effect-of-rehabilitation-at-moderate-altitude-on-airway-resistance-measured-with-forced-oscillation-technique-in-copd-patients-100597828","NCT07063563","Effect of Rehabilitation at Moderate Altitude on Airway Resistance Measured With Forced Oscillation Technique in COPD-patients","Effect of Rehabilitation at Moderate Altitude on Airway Resistance Measured With Forced Oscillation Technique in Patients With COPD","Inclusion Criteria:\n\n* Aged ≥18 years\n* Stable clinical condition for \\>3 weeks (e.g., no exacerbations)\n* Resting SpO₂ ≥88% and exercise-induced hypoxemia defined as a drop in SpO₂ of ≥4% and\u002For a level below 90% during the 6MWT\n* Informed consent documented by signature\n\nExclusion Criteria:\n\n* Severe daytime resting hypoxemia (SpO₂ \\\u003C88%)\n* Long-term oxygen therapy\n* Unstable clinical condition requiring adjustment of pharmacological or other treatment modalities, need for intensive care, or presence of relevant severe comorbidities\n* Inability to comply with study procedures (e.g., due to language barriers, psychological disorders, neurological or orthopedic impairments, walking disability, or inability to ride a bicycle)\n* Women who are pregnant or breastfeeding\n* Enrolment in another clinical trial involving active treatment",{"count":79,"type":19},52,[52],"Airway resistance will be measured using the forced oscillation technique (FOT). The parameters Rrs, Xrs, and ∆Xrs will be compared before and after a pulmonary rehabilitation cycle at moderate altitude. Additionally, the differences between low and moderate altitude will also be examined.",[57],[84,85,86],"Oxygen","Exercise","Rehabilitation","2025-07-16",{"date":89,"type":32},"2025-07-20",{"date":91,"type":19},"2025-07-23",{"date":93,"type":19},"2025-12-31",{"name":38,"class":39},2,{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":101,"acronym":4,"eligibilityCriteria":102,"healthyVolunteers":103,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":104,"targetDuration":4,"studyType":50,"phases":106,"briefSummary":107,"conditions":108,"keywords":111,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":117,"lastUpdatePostDateStruct":118,"startDateStruct":120,"completionDateStruct":122,"leadSponsor":123,"locationsCount":40},"100572816","bliib-fit---mach-mit-in-residential-care-facilities-100572816","NCT06738186","\"Bliib Fit - Mach Mit!\" in Residential Care Facilities","\"Bliib Fit - Mach Mit!\" in Alters- Und Pflegeinstitutionen","Inclusion Criteria:\n\n* Written informed consent\n* Low to moderate risk of falling\n* Physically and cognitively able to independently carry out exercise instructions (based on referral of clinical staff on site)\n* Mini Mental State Examination (MMSE) test score ≥ 20\n\nExclusion Criteria:\n\n* Inability to speak or understand German\n* High risk of falling\n* Unstable cardiovascular condition or other health condition, which does not support a safe participation in exercise program (based on referral of clinical staff on site, patient file)\n* Scheduled transfer to another institution within the next 3 months",true,{"count":105,"type":19},40,[52],"The goal of this clinical trial is to learn, if the video-based exercise program \"Bliib fit - mach mit!\" can be used to improve physical fitness in older adults living in residential care facilities. The main questions it aims to answer are:\n\nDoes the video-based exercise program improve participants' physical fitness? Does the video-based exercise program improve participants' quality of life, perceived fall risk, self-efficacy and daily physical activity levels?\n\nResearchers will compare this exercise program to an optimized standard care activation program (caregiver-led) to see if the video-based program can affect physical fitness in older adults living in residential care facilities.\n\nParticipants will participate in the exercise or activation program for 12 weeks, four times a week, with each session lasting 20 minutes.",[109,110],"Physical Fitness in Older Adults","Exercise Program",[112,113,114,115,116],"physical activity promotion","exercise","physical fitness","elderly","residential care facility","2024-12-12",{"date":119,"type":32},"2024-12-17",{"date":121,"type":32},"2024-12-05",{"date":93,"type":19},{"name":38,"class":39},{"id":125,"slug":126,"hasResults":11,"nctId":127,"briefTitle":128,"officialTitle":129,"acronym":130,"eligibilityCriteria":131,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":132,"targetDuration":4,"studyType":50,"phases":134,"briefSummary":135,"conditions":136,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":142,"lastUpdatePostDateStruct":143,"startDateStruct":145,"completionDateStruct":147,"leadSponsor":149,"locationsCount":40},"100564635","exergaming-revolution-in-dementia-100564635","NCT06631742","Exergaming Revolution in Dementia","The Effect of an Exergaming Intervention on Physical Activity and Sleep in People With Major Neurocognitive Disorders Living in Long-term Care Facilities: a Pilot Randomized Controlled Trial.","GameDementia","Inclusion Criteria:\n\n* Neurocognitive disorder based on Alzheimer's Disease, Parkinson's disease, Lewy body dementia or Mixed dementia according to the criteria of the American Psychiatric Association: Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM 5)\n* Mini-Mental-Status-Examination (MMSE) Score of ≥5 and ≤26 out of e maximum of 30\n\nExclusion Criteria:\n\n* MMSE \\\u003C5\n* Unstable cardiovascular condition or other medical condition that does not allow for safe participation according to the recommendations of the American College of Sports Medicine\n* Planned transfer to another facility within the next 3 months\n* Acute behavioural problems",{"count":133,"type":19},48,[52],"This pilot randomized controlled trial evaluates the effect of a 12 weeks exergaming training in people with major neurocognitive disorders (MNCD) living in long-term care facilities.",[137,138,139,140,141],"Major Neurocognitive Disorder","Alzheimer Disease","Parkinson Disease","Lewy Body Dementia","Mixed Dementias","2024-10-07",{"date":144,"type":32},"2024-10-08",{"date":146,"type":32},"2024-09-27",{"date":148,"type":19},"2027-04-30",{"name":38,"class":39},""]