[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"chronic-respiratory-disease\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:chronic-respiratory-disease":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,45,75,105,131,151,170],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100560627","the-benefits-of-individualized-follow-up-with-a-sport-health-professional-in-the-care-of-patients-with-chronic-respiratory-diseases-100560627",false,"NCT06579612","The Benefits of Individualized Follow-up With a Sport-Health Professional in the Care of Patients With Chronic Respiratory Diseases","The Benefits of Individualized Follow-up With a Sport-Health Professional in the Care of Patients With Chronic Respiratory Diseases, to Maintain Long-term Benefits After a Respiratory Rehabilitation Program","WANTTOMOVE","Inclusion Criteria:\n\n* Diagnosis of one or more chronic respiratory diseases (asthma, chronic obstructive pulmonary disease, diffuse interstitial lung disease, bronchiectasis, obstructive sleep apnea syndrome, etc.).\n* Participation in a respiratory pulmonary program\n* Have given consent\n* Patient of legal age\n* Patient affiliated to Social Security\n\nExclusion Criteria:\n\n* Any medical contraindication to the practice of adapted physical activity in rehabilitation\n* Patients under guardianship or curatorship\n* Patients deprived of their liberty\n* Patients over 80 years of age at the time of inclusion.","ALL","18 Years","80 Years",{"count":21,"type":22},352,"ESTIMATED","INTERVENTIONAL",[25],"NA","Pulmonary rehabilitation is an integral part of care for patients with chronic respiratory diseases. It improves patients' physical capacities, quality of life and symptoms, at least in the short term.\n\nThe hypothesis that patients receiving personalized support from a professional following pulmonary rehabilitation will maintain long-term benefits.\n\nThis study concerns patients with a diagnosis of one or more chronic respiratory diseases.\n\nIt is a multicenter, blinded, randomized controlled superiority trial in 2 parallel arms:\n\n* a group comparing follow-up and personalized support after a pulmonary rehabilitation program (experimental group)\n* a control group receiving only usual care",[28],"Chronic Respiratory Disease",[30,31],"chronic respiratory disease","pulmonary rehabilitation","RECRUITING","2026-06-24",{"date":35,"type":36},"2026-06-26","ACTUAL",{"date":38,"type":36},"2024-11-07",{"date":40,"type":22},"2029-11-07",{"name":42,"class":43},"University Hospital, Brest","OTHER",2,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":17,"minAge":53,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":74},"100346933","genesis-electrical-impedance-tomography-eit-a-preliminary-study-100346933","NCT03797183","Genesis Electrical Impedance Tomography (EIT): A Preliminary Study","The Associations Between EIT and Clinical Measures During Standard of Care Procedures in Patients With Respiratory Disease: A Preliminary Study","Inclusion Criteria:\n\n* 2 weeks old - 40 years old\n* Premature infants with current age \\>2 weeks with a confirmed diagnosis of BPD based on NIH criteria\n* Or Chronic respiratory disease due to underlying neuromuscular disease\n* Or confirmed neuromuscular disease with an echo completed within the preceding 12 months of study participation of DMD or other diagnoses associated with mild cardiomyopathy.\n* have had a VQ scan\n* will be undergoing cardiac catherization for for pulmonary vein stenosis, pulmonary hypertension and\u002For pulmonary artery stenosis\n* Or healthy controls\n\nExclusion Criteria:\n\n* \\\u003C2 weeks of age\n* Congenital diaphragmatic hernia\n* Severe congenital heart disease\n* Significant genetic abnoralities\n* Anything that interferes with lead placement on the chest wall\n* Unwilling\u002Frefusal to sign consent\n* Pregnant or lactating\n* Pacemaker of other surgical implant and spinal implant (causes noise in the data)\n* Moderate to severe cardiomyopathy\n* Patients with temporary cognitive disability due to illness",true,"14 Days","40 Years",{"count":56,"type":22},90,"OBSERVATIONAL","The purpose of this study is to evaluate the Genesis Electrical Impedance Tomography (EIT) imaging system for use in pediatric respiratory disease populations including neuromuscular and bronchopulmonary dysplasia, as well as in age and height matched controls. The EIT does not use radiation, and is read through electrodes.",[60,28,61,62,63,64],"Premature Infant","Neuromuscular Diseases","Healthy","Bronchopulmonary Dysplasia","Pulmonary Vein Stenoses","2025-11-11",{"date":67,"type":36},"2025-11-13",{"date":69,"type":36},"2019-05-03",{"date":71,"type":22},"2026-11",{"name":73,"class":43},"University of Colorado, Denver",1,{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":4,"eligibilityCriteria":81,"healthyVolunteers":11,"sex":17,"minAge":82,"maxAge":4,"enrollmentInfo":83,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":85,"conditions":86,"keywords":92,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":74},"100569263","aevicemd-for-detection-of-wheeze-in-pediatric-and-adult-populations-100569263","NCT06691971","AeviceMD for Detection of Wheeze in Pediatric and Adult Populations","A Pilot Study to Assess Aevice Medical Device for Detection of Wheeze in Pediatric and Adult Populations","Inclusion Criteria:\n\n* The subject is willing and\u002For parents\u002Fguardians are able to give informed consent for participation in the study.\n* Male or Female, aged ≥ 3 years.\n* Diagnosed with acute asthma exacerbation by an ED provider.\n\nExclusion Criteria:\n\n* Any other significant disease or disorder which, in the opinion of the Investigator, may either put the subjects at risk because of participation in the study, or may influence the result of the study, or the subject's ability to participate in the study.","3 Years",{"count":84,"type":22},160,"Respiratory signs and symptoms consisting of wheeze, cough, and breathlessness are obtained in a manual fashion through history taking and physical examination by the healthcare professional. Auscultation of the lung assesses airflow through the trachea-bronchial tree and is helpful in diagnosing various respiratory disorders. AeviceMD is a wearable device that can acquire and process lung sounds, thus assisting in the detection of abnormal lung sounds. The primary objective of this study is to determine if AeviceMD can detect wheeze of pediatrics and adults as accurately as a physician through auscultation. The secondary objective is to investigate if AeviceMD can be used for remote auscultation of breath sounds.",[87,88,89,90,91,28],"Subject Presenting Wheeze","Asthma","Bronchial Disease","Respiratory Tract Diseases","Pediatric Asthma",[93,94,95],"Wheeze","Auscultation","Wearable Medical Device","2025-09-30",{"date":98,"type":36},"2025-10-03",{"date":100,"type":36},"2023-06-29",{"date":102,"type":22},"2026-12",{"name":104,"class":43},"Aevice Health Pte. Ltd.",{"id":106,"slug":107,"hasResults":11,"nctId":108,"briefTitle":109,"officialTitle":109,"acronym":4,"eligibilityCriteria":110,"healthyVolunteers":52,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":111,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":113,"conditions":114,"keywords":115,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":125,"completionDateStruct":127,"leadSponsor":129,"locationsCount":74},"100551355","takingcare---tackling-the-needs-of-carers-of-people-with-chronic-respiratory-diseases-100551355","NCT06459011","TAKINGCARE - TAcKlING the Needs of Carers of People With Chronic respirAtoRy disEases","Inclusion Criteria:\n\n* People with chronic respiratory diseases (CRD):\n\n  * 18 years of age or older;\n  * Diagnosed with ILD, COPD, lung cancer, severe asthma or bronchiectasis;\n  * Fluent in Portuguese;\n  * Identify an informal\u002Ffamily carer;\n* Informal carers of people with CRD:\n\n  * 18 years of age or older;\n  * Fluent in Portuguese.\n* Health Professionals:\n\n  * Fluent in Portuguese;\n  * Contact with people with CRD in their clinical practice.\n\nExclusion Criteria:\n\n* People with CRD:\n\n  * Signs of cognitive impairment in the Six-item Cognitive Impairment Test (6CIT) for the interviews.\n* Informal carers of people with CRD:\n\n  * Signs of cognitive impairment in the 6CIT.",{"count":112,"type":22},250,"This study aims to: i) develop an instrument that assesses the needs of informal carers of people with chronic respiratory diseases (CRD), along diseases' trajectory, and evaluate its measurement properties; ii) identify existing instruments that assess the needs of informal\u002Ffamily carers and their measurement properties, iii) characterize the needs of informal carers of people with CRD and iv) characterize the health literacy of informal carers of people with CRD.\n\nThe first task will be a systematic review. For the second and third tasks, people with CRD, their informal carers and health professionals will be recruited via the pulmonology services from the hospitals:Unidade Local de Saúde de Gaia\u002FEspinho, Unidade Local de Saúde da Região de Aveiro, and Unidade Local de Saúde de Entre o Douro e Vouga. On task 2, a mixed-methods study will be conducted to characterize the needs of informal carers of people with CRD, as well as their health literacy. On task 3, an instrument that assesses the needs of informal carers of people with CRD will be developed and its measurement properties will be studied.\n\nThis study is urgently needed to provide meaningful support to this hidden workforce who provides most of the care to people with DRC contributing to guide meaningful supportive care to this population and their loved ones.",[28],[30,116,117,118,119,120,121],"needs","informal care","loved ones","health literacy","measurement properties","preparedness for caregiving","2024-12-12",{"date":124,"type":36},"2024-12-17",{"date":126,"type":36},"2024-06-24",{"date":128,"type":22},"2028-07-31",{"name":130,"class":43},"Aveiro University",{"id":132,"slug":133,"hasResults":11,"nctId":134,"briefTitle":135,"officialTitle":136,"acronym":4,"eligibilityCriteria":137,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":138,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":140,"conditions":141,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":142,"lastUpdatePostDateStruct":143,"startDateStruct":145,"completionDateStruct":147,"leadSponsor":149,"locationsCount":74},"100556496","observing-physiological-changes-in-patients-with-long-term-oxygen-therapy-100556496","NCT06525857","Observing Physiological Changes in Patients With Long-term Oxygen Therapy","Observing Physiological Changes in Patients With Long-term Oxygen Therapy Via Optical and Accelerometry Signals","Inclusion Criteria:\n\n* Age ≥ 18-year-old, and\n* Chronic respiratory disease including a) chronic obstructive pulmonary disease, b) interstitial lung disease, c) pulmonary hypertension, d) bronchiectasis, and\n* Prescribed new LTOT due to a chronic respiratory disease with resting and\u002For exertional hypoxemia, and\n* Able to speak\u002Fread\u002Funderstand German or French, and\n* Willing and able to understand and provide signed informed consent\n\nExclusion Criteria:\n\n* Pregnant or lactating women, or\n* Inability to follow the procedures\u002Finstructions of the study (e.g. due to language, psychological disorders, dementia, etc.), or\n* Patients having a subordination link to the investigators, or\n* Patients with isolated nocturnal oxygen therapy or LTOT prescription for a heart disease, sleep associated breathing disorder, neuromuscular disease or lung cancer, or\n* Known participation in another human research project (ClinO\u002FHRO) that may affect the objectives of this study.",{"count":139,"type":22},40,"In this project, the investigators aim to assess changes of physiological parameters obtained non-invasively through PPG and accelerometry signals between before and during LTOT (long-term oxygen therapy) and investigate if those changes are different in patients with worsening frailty and\u002For improving quality of life.\n\nFor this, they will record optical (PPG) and accelerometry data via a datalogger on 40 patients undergoing LTOT and assess the PPG-derived physiological signals.",[28],"2024-07-25",{"date":144,"type":36},"2024-07-29",{"date":146,"type":36},"2024-06-01",{"date":148,"type":22},"2026-01-31",{"name":150,"class":43},"Insel Gruppe AG, University Hospital Bern",{"id":152,"slug":153,"hasResults":11,"nctId":154,"briefTitle":155,"officialTitle":156,"acronym":4,"eligibilityCriteria":157,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":158,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":160,"conditions":161,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":142,"lastUpdatePostDateStruct":162,"startDateStruct":164,"completionDateStruct":166,"leadSponsor":168,"locationsCount":74},"100502324","tele-rehabilitation-in-chronic-respiratory-disease-an-observational-cohort-study-100502324","NCT05820776","Tele-rehabilitation in Chronic Respiratory Disease: an Observational Cohort Study","Remote Exercise-based Pulmonary Rehabilitation Telemedicine in Chronic Respiratory Disease: an Observational Cohort Study","Inclusion Criteria:\n\n* stable chronic respiratory disease\n* qualified candidates for pulmonary rehabilitation,\n* current non-smoker;\n* primary diagnosis chronic respiratory disease limited by dyspnea (mMRC≥2);\n* free of exacerbation at the time of admission, and\n* stable co-existing conditions\n\nExclusion Criteria:\n\n* completed PR within the previous 12 months of the current admission and\n* being unable to communicate with the treating team.",{"count":159,"type":22},50,"Pulmonary rehabilitation is a program that helps people with lung disease improve their function. It uses exercise, education, and self-management strategies to improve physical ability and quality of life. Because some people are unable to visit West Park Healthcare Centre, we established a remote supervised pulmonary rehabilitation program that patients can access via an electronic device (computer, tablet or smart phone). Regular quality assurance is necessary to ensure that the program is effective. We plan to collect and summarize the program's results. The benefit of doing so is that it allows us to make any changes or improvements that may help patients with chronic respiratory conditions.",[28],{"date":163,"type":36},"2024-07-26",{"date":165,"type":36},"2023-04-06",{"date":167,"type":22},"2025-12-31",{"name":169,"class":43},"West Park Healthcare Centre",{"id":171,"slug":172,"hasResults":11,"nctId":173,"briefTitle":174,"officialTitle":175,"acronym":4,"eligibilityCriteria":176,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":177,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":179,"conditions":180,"keywords":187,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":192,"lastUpdatePostDateStruct":193,"startDateStruct":195,"completionDateStruct":197,"leadSponsor":199,"locationsCount":74},"100458345","the-long-term-spill-over-impact-of-covid-19-on-health-and-healthcare-of-people-with-non-communicable-diseases-100458345","NCT05248412","The Long-term Spill-over Impact of COVID-19 on Health and Healthcare of People With Non-communicable Diseases","The Long-term Spill-over Impact of COVID-19 on Health and Healthcare of Patients With Non-communicable Diseases (and Without COVID-19) : an In-depth Outcome and Health Economic Evaluation","(For cohort study)\n\nInclusion Criteria:\n\n* People aged 18 years or above with a documented doctor-diagnosed NCDs (diabetes mellitus, hypertension, cardiovascular disease, cancer, chronic kidney disease, or chronic respiratory disease )\n* People who attended at least once HA hospitals, general or specialist out-patients clinics between 1 January 2010 and 31 December 2024\n\nExclusion Criteria:\n\n\\- People with a documented doctor-diagnosed COVID-19\n\n(For cross-sectional study)\n\nInclusion Criteria:\n\n* People aged 18 years or above with a documented doctor-diagnosed NCDs (diabetes mellitus, hypertension, cardiovascular disease, cancer, chronic kidney disease, or chronic respiratory disease )\n* All participants are able to communicate in either Chinese or English and provide informed consent.\n\nExclusion Criteria:\n\n* People with a documented diagnosis of COVID-19 during the study period.",{"count":178,"type":22},250000,"Objectives and aim: To evaluate the long-term spill-over (indirect) effect of Coronavirus disease (COVID-19) on health outcomes and healthcare utilization among people with non-communicable diseases and without COVID-19.\n\nDesign: A population-based cohort study using electronic health records of the Hospital Authority (HA) clinical management system, economic modeling, and serial cross-sectional surveys on healthcare service utilization.\n\nSetting: HA public hospitals and outpatient clinics in Hong Kong\n\nParticipants: People aged ≥ 18 years with a documented diagnosis of diabetes mellitus, hypertension, cardiovascular disease, cancer, chronic respiratory disease, and chronic kidney disease; without COVID-19; attending HA services between 2010 and 2024.\n\nMain outcome measures: All-cause mortality, disease-specific outcomes, healthcare service utilization, and costs.\n\nMethods: The annual incidence of each outcome in each year between 2010 and 2024 will be calculated. An interrupted time-series analysis to assess the changes in outcomes between pre-and-post-COVID-19 outbreak periods. Long term health economic impact of healthcare disruptions during the COVID-19 outbreak will be modeled using microsimulation. Multivariable Cox proportional hazards regression and Poisson\u002Fnegative binomial regression to evaluate the effect of different modes of care on the risk of the outcomes.\n\nImplications: Findings will inform policies and practices on contingency care plans to avoid excessive morbidity and mortality and to assure the quality of care for patients with NCD as part of the territorial response to the health crisis.",[181,182,183,184,28,185,186],"Diabetes Mellitus","Hypertension","Cancer","Cardiovascular Diseases","Kidney Disease, Chronic","Noncommunicable Diseases",[188,189,190,191,186],"COVID-19 Pandemic","Morality","Complication","Utilization, Health Care","2022-02-20",{"date":194,"type":36},"2022-03-08",{"date":196,"type":36},"2021-06-21",{"date":198,"type":22},"2026-06-30",{"name":200,"class":43},"The University of Hong Kong"]