[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100630325":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":28,"centralContacts":24,"locations":33,"responsibleParty":54,"collaborators":24,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":63,"eligibilityCriteria":64,"healthyVolunteers":59,"sex":65,"minAge":66,"maxAge":24,"enrollmentInfo":67,"targetDuration":24,"studyType":70,"phases":71,"briefSummary":73,"conditions":74,"keywords":80,"overallStatus":35,"whyStopped":24,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":111},{"fullName":5,"class":6},"Hospital de Granollers","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Standard ILD Follow-Up Pathway","ACTIVE_COMPARATOR","Participants in this arm will follow the standard ILD follow-up pathway, in which routine components of ILD monitoring-such as pulmonary function tests, six-minute walk test when performed, laboratory analyses, imaging when clinically indicated, pharmacy consultations, nursing assessments and medical visits-are scheduled independently by each department according to routine workflows and availability. These procedures usually take place on separate days, and completing a full follow-up cycle commonly requires multiple hospital visits. The organizational structure of care, scheduling processes and clinical content remain unchanged.",[13],"Other: Standard ILD Follow-Up Pathway",{"label":15,"type":16,"description":17,"interventionNames":18},"Optimized One-Day ILD Follow-Up Circuit","EXPERIMENTAL","Participants in this arm will follow an optimized coordinated ILD follow-up circuit in which all required procedures are pre-scheduled and consolidated into a single structured one-day visit. This includes medical consultation, nursing assessment, pharmacy review, pulmonary function testing, laboratory analyses and imaging when clinically indicated. When needed, rheumatology or internal medicine evaluation is incorporated into the same coordinated visit. The intervention does not introduce new tests, does not modify clinical decision-making and does not alter hospital prioritization or waiting-list rules; it reorganizes the timing and coordination of existing procedures to reduce fragmentation and overall time burden.",[19],"Other: Optimized One-Day ILD Follow-Up Circuit",[21,25],{"type":6,"name":9,"description":22,"armGroupLabels":23,"otherNames":24},"Organizational usual-care comparator consisting of the standard ILD follow-up pathway. For patients with established ILD receiving antifibrotic and\u002For immunosuppressive therapy, follow-up components such as pulmonary function tests, 6-minute walk test when performed, laboratory monitoring, imaging when indicated, pharmacy visits, nursing assessments, and medical consultations are requested and scheduled independently by each department according to routine workflows and waiting times. These procedures usually occur on separate days, and a full follow-up cycle frequently requires multiple hospital visits. The study team does not alter scheduling priorities, clinical decisions, or the type of tests performed.",[9],null,{"type":6,"name":15,"description":26,"armGroupLabels":27,"otherNames":24},"Organizational intervention that coordinates and bundles all required ILD follow-up procedures into a single structured \"one-day\" visit. For patients with established ILD on antifibrotic and\u002For immunosuppressive therapy, the intervention pre-schedules pulmonary function tests, laboratory monitoring, imaging when indicated, pharmacy consultation, nursing assessment, and medical visits within the same day. When clinically necessary, rheumatology or internal medicine consultations are integrated into the same coordinated circuit. The intervention does not introduce new tests or treatments and does not modify hospital waiting-list rules; it only reorganizes the timing and consolidation of existing follow-up procedures to reduce overall time burden.",[15],[29],{"name":30,"affiliation":31,"role":32},"Jaume Bordas-Martinez, MD, PhD","Hospital General de Granollers","PRINCIPAL_INVESTIGATOR",[34],{"facility":31,"status":35,"city":36,"state":37,"zip":38,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"RECRUITING","Granollers","Barcelona","08402","Spain","ES",{"type":42,"coordinates":43},"Point",[44,45],2.28773,41.60797,{"lat":45,"lon":44},[48],{"name":49,"role":50,"phone":51,"phoneExt":52,"email":53},"Jaume Bordas-Martínez, MD, PhD","CONTACT","+34 938 425 000","+34 938 425 00","jbordas@fphag.org",{"type":32,"investigatorFullName":55,"investigatorTitle":56,"investigatorAffiliation":5,"oldNameTitle":24,"oldOrganization":24},"Jaume Bordas-Martinez","Principal Investigator","100630325","optimizing-the-follow-up-journey-in-interstitial-lung-disease-the-optimize-ild-2-trial-100630325",false,"NCT07486206","Optimizing the Follow-Up Journey in Interstitial Lung Disease: The OPTIMIZE-ILD-2 Trial","OPTIMIZE-ILD-2: A Randomized, Pragmatic, Parallel-Group Trial Evaluating the Impact of an Optimized Coordinated Follow-Up Circuit on Time Burden in Patients With Interstitial Lung Disease","OPTIMIZE-ILD-2","Inclusion Criteria:\n\n* Age ≥ 18 years.\n* Established diagnosis of interstitial lung disease (ILD).\n* Currently receiving antifibrotic therapy, immunosuppressive therapy, or both, as part of routine ILD care.\n* Under active follow-up at the participating ILD center.\n* Able to attend the required follow-up procedures included in the study visit.\n* Able to provide informed consent.\n\nExclusion Criteria:\n\n* Inability to complete the coordinated follow-up visit for non-medical reasons (e.g., logistical impossibility).\n* Clinical instability or acute illness interfering with planned follow-up procedures (such as respiratory infection, suspected ILD exacerbation, acute heart failure, or other acute conditions).\n* Participation in another interventional clinical trial that may alter visit frequency or follow-up structure.\n* Cognitive impairment preventing informed consent or completion of questionnaires.\n* Patient refusal to participate or refusal to allow data collection.","ALL","18 Years",{"count":68,"type":69},152,"ESTIMATED","INTERVENTIONAL",[72],"NA","The OPTIMIZE-ILD-2 trial is a prospective, randomized, open-label clinical trial designed to evaluate the impact of a coordinated follow-up pathway on patients with established interstitial lung disease (ILD). In routine clinical practice, follow-up workflows for ILD are frequently fragmented, requiring multiple hospital visits for pulmonary function tests, laboratory analysis, treatment administration, and consultations with various specialists, which increases the burden for both patients and caregivers. This study compares the standard follow-up care against an optimized circuit where all routine monitoring procedures and interdisciplinary consultations are pre-bundled and scheduled within a single, coordinated hospital visit.\n\nAll eligible patients under active ILD follow-up are included consecutively to ensure a pragmatic, real-world representation of the treated ILD population. The primary objective is to measure the total follow-up time burden, defined as the total home-to-home time required to complete the follow-up circuit. As a cross-sectional assessment within a longitudinal context, secondary objectives include assessing socioeconomic cost-burden, the environmental carbon footprint of the follow-up journey, health-related quality of life, and clinical frailty. Caregiver-related outcomes, including burden and experience measures, are contingent upon the presence of a primary caregiver and the provision of their independent informed consent.\n\nThe design of this protocol was informed by a patient focus group and is officially endorsed by the 'AIRE' Associació Catalana de Malalts i Trasplantats Pulmonars, ensuring a patient-centered approach that prioritizes follow-up efficiency and human impact.",[75,76,77,78,79],"Interstitial Lung Disease (ILD)","Fibrotic Interstitial Lung Disease","Idiopathic Pulmonary Fibrosis (IPF)","Progressive Pulmonary Fibrosis","Interstitial Lung Disease Due to Connective Tissue Disease (Disorder)",[81,82,83,84,78,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101],"Interstitial Lung Disease","ILD","Pulmonary Fibrosis","Idiopathic Pulmonary Fibrosis","CTD-ILD","Fibrotic ILD","Antifibrotic Therapy","Immunosuppressive Therapy","Follow-Up Pathway","Follow-Up Care Coordination","Time Burden","Home-to-Home Time Burden","One-Day ILD Clinic","Health Services Research","Patient-Centered Follow-Up","Organizational Intervention","Pulmonary Function Tests","Quality of Life","Patient Experience","Carbon Footprint","Multidisciplinary Care","2026-04-06",{"date":104,"type":105},"2026-04-09","ACTUAL",{"date":107,"type":105},"2026-03-09",{"date":109,"type":69},"2028-03-01",{"name":5,"class":6},1]