[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"occupational-diseases\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:occupational-diseases":42},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,83,115,150,193,221,250,270],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":45,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":82},"100641995","human-observatory-study-100641995",false,"NCT07646782","Human Observatory Study","The Human Observatory: A Prospective Individual and Population-Level Study of Aging, Health, and Longevity","HOS","Inclusion Criteria:\n\n* Enrolled in the 100-Year Human Aging Study at any fixed or mobile clinical site; OR completion of online health screener with provision of geographic anchor data and consent.\n\nExclusion Criteria:\n\n* Age under 18 years (current protocol; pediatric amendment planned).",true,"ALL","18 Years",{"count":21,"type":22},1000000,"ESTIMATED","OBSERVATIONAL","The Human Observatory Study is a prospective observational and ecological surveillance study building a continuously-updating world model for human health, disease, and death at the individual and population level. Individual multi-system clinical data from enrolled participants are linked to a continuously-ingested ecological data infrastructure spanning environmental exposures, social determinants, genealogical and family history records, mortality data, and population health databases at geographic resolutions from home address to global scale and beyond. The resulting model generates individual screening recommendations informed by population-level causal estimates, and population-level causal forecasts anchored by present-timepoint individual clinical biology. Thus creating a feedback architecture designed to improve both simultaneously.",[26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44],"Aging","Mortality","All-cause Mortality","Life Expectancy","Cardiovascular Diseases","Neoplasms","Cognitive Dysfunction","Metabolic Syndrome","Frailty","Musculoskeletal Disease","Neurodegenerative Disease","Dementia","Activities of Daily Living","Health Related Quality of Life","Disability Physical","Environmental Exposure","Occupational Diseases","Health Equity","Social Determinants of Health",[46,47,48,49,50,51,52,53,54,55,56,57,58,43,59,60,61,62,63,64,65,66,67,68,69],"longevity","biological aging","causal inference","life expectancy","exposome","Environmental Health","Social Determinants","Genealogy","Family History","Human Family Tree","Population Health","Neighborhood Health","Geographic Health Disparities","Mortality Prediction","Biomarker Validation","Cardiopulmonary Exercise Testing","Body Composition","Preventive Medicine","Healthspan","Functional Decline","Centenarian","Space Medicine","Aerospace Medicine","World Model","RECRUITING","2026-06-09",{"date":73,"type":74},"2026-06-15","ACTUAL",{"date":76,"type":74},"2026-04-25",{"date":78,"type":22},"2099-12-31",{"name":80,"class":81},"Longevity Metrics, Inc.","INDUSTRY",1,{"id":84,"slug":85,"hasResults":11,"nctId":86,"briefTitle":87,"officialTitle":88,"acronym":4,"eligibilityCriteria":89,"healthyVolunteers":11,"sex":18,"minAge":90,"maxAge":91,"enrollmentInfo":92,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":94,"conditions":95,"keywords":98,"overallStatus":104,"whyStopped":4,"lastUpdateSubmitDate":105,"lastUpdatePostDateStruct":106,"startDateStruct":108,"completionDateStruct":110,"leadSponsor":112,"locationsCount":82},"100621209","development-of-multidimensional-screening-tool-for-wmsds-100621209","NCT07367646","Development of Multidimensional Screening Tool for WMSDs","Development and Validation of a Multidimensional Screening Tool for Work-Related Musculoskeletal Disorders: A COSMIN-Guided Psychometric Study","Inclusion Criteria:\n\n* Current regular employees working at the study site.\n* Adults aged 19 years or older who understand the study purpose and procedures and voluntarily agree to participate in writing.\n* Participants capable of reading, understanding, and self-responding to the questionnaire.\n* Individuals with musculoskeletal symptoms according to NIOSH standards: symptoms lasting more than one week OR recurring at least once a month in the past 12 months (symptoms include pain, aching, stiffness, burning sensation, tingling, or numbness).\n\nExclusion Criteria:\n\n* Individuals with cognitive or mental impairments that make it difficult to understand the study or complete the survey.\n* Individuals suspected of having a medical emergency or severe disease requiring immediate medical attention.\n* Individuals deemed unsuitable for participation by the researcher.","19 Years","65 Years",{"count":93,"type":22},250,"The purpose of this study is to develop a multidimensional screening tool for Work-Related Musculoskeletal Disorders (WMSDs) and to evaluate its psychometric properties. The study involves a cross-sectional survey of approximately 250 workers in the bio-pharmaceutical industry to assess the tool's structural validity, internal consistency, construct validity, and measurement invariance following COSMIN guidelines.",[96,97,42],"Work-Related Musculoskeletal Disorders","Musculoskeletal Diseases",[99,100,101,102,103],"WMSDs","Musculoskeletal Pain","Screening Tool","Psychometrics","Occupational Health","NOT_YET_RECRUITING","2026-04-22",{"date":107,"type":74},"2026-04-24",{"date":109,"type":22},"2026-06-20",{"date":111,"type":22},"2026-12-31",{"name":113,"class":114},"Sahmyook University","OTHER",{"id":116,"slug":117,"hasResults":11,"nctId":118,"briefTitle":119,"officialTitle":119,"acronym":120,"eligibilityCriteria":121,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":122,"targetDuration":4,"studyType":124,"phases":125,"briefSummary":127,"conditions":128,"keywords":134,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":140,"lastUpdatePostDateStruct":141,"startDateStruct":143,"completionDateStruct":145,"leadSponsor":147,"locationsCount":149},"100571143","confirming-the-effects-of-acupuncture-treatments-to-relieve-symptoms-of-gulf-war-illness-100571143","NCT06716411","Confirming the Effects of Acupuncture Treatments to Relieve Symptoms of Gulf War Illness","CARE","Inclusion Criteria:\n\n* Deployed to the Gulf Theater of operations (as defined by 38 CFR 3.317, includes Iraq, Kuwait, Saudi Arabia, Bahrain, Qatar, the United Arab Emirates, Oman, the Gulf of Aden, the Gulf of Oman, the Persian Gulf, the Arabian Sea, the Red Sea, and the airspace above all of these locations) between August 1990 and the present date\n* Have at least 2 of the following symptoms from the 3 CDC clusters of symptom that have lasted for more than 6 months. Each symptom cluster must be characterized as mild-moderate or severe, with at least one symptom in each cluster required to be severe. The clusters are:\n\nA. Fatigability: fatigue 24 hours or more after exertion B. Mood and Cognition: feeling depressed; feeling irritable; difficulty thinking or concentrating; feeling worried, tense, anxious; problems finding words; or problems getting to sleep C. Musculoskeletal: joint pain or muscle pain\n\nExclusion Criteria:\n\n* Currently enrolled in another clinical trial\n* Have another disease that likely could account for the symptoms, as determined by our Medical Monitor\n* Severe psychiatric illness (in the last 2 years psychiatric hospitalization, suicidal attempt, alcohol or substance abuse, use of antipsychotic medication) as measured by the Primary Care Evaluation of Mental Disorder (Prime MD).\n* Unable to complete the protocol on based on the evaluation of the Medical Monitor.",{"count":123,"type":22},200,"INTERVENTIONAL",[126],"NA","This unblinded Phase II clinical trial will test the effects of individualized acupuncture treatments offered in extant acupuncture practices in the community; practitioners will have had at least 5 years of experience plus additional training provided by the study. Veterans with diagnosed symptoms of Gulf War Illness will be randomized to either six months of biweekly acupuncture treatments (group 1, n=100) or 2 months of waitlist followed by weekly acupuncture treatments (group 2, n=100). Measurements were taken at baseline, 2, 4 and 6 months. The primary outcome is the SF-36 physical component scale score (SF-36P).",[129,130,131,42,132,133],"Persian Gulf Syndrome","Gulf War Syndrome","Multiple Chronic Illnesses","War-Related Injuries","Wounds and Injuries",[135,136,137,138,139],"Acupuncture","Gulf War Illness","Complex Medical Illness","Chronic Multisymptom Illness","Veteran","2026-04-02",{"date":142,"type":74},"2026-04-03",{"date":144,"type":74},"2026-02-03",{"date":146,"type":22},"2028-09-30",{"name":148,"class":114},"University of Utah",10,{"id":151,"slug":152,"hasResults":11,"nctId":153,"briefTitle":154,"officialTitle":155,"acronym":156,"eligibilityCriteria":157,"healthyVolunteers":17,"sex":18,"minAge":158,"maxAge":91,"enrollmentInfo":159,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":161,"conditions":162,"keywords":171,"overallStatus":104,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":185,"startDateStruct":187,"completionDateStruct":189,"leadSponsor":191,"locationsCount":82},"100632676","neck-musculoskeletal-symptoms-among-turkish-endodontists-100632676","NCT07516782","Neck Musculoskeletal Symptoms Among Turkish Endodontists","Analysis of Neck Musculoskeletal Symptoms, Functional Parameters, and Associated Factors in Turkish Endodontists","ENDO-NECK","Inclusion Criteria:\n\n* Aged 25 to 65 years\n* Actively practicing as an endodontist in Turkey in public institutions, university hospitals, or the private sector\n* Willing and able to provide informed consent\n* Endodontists with or without neck pain\n\nExclusion Criteria:\n\n* History of cervical spine surgery within the last 3 months\n* History of cervical spine infection within the last 3 months (e.g., spondylodiscitis)\n* History of malignancy involving the cervical region\n* Spinal cord compression due to tumor or another cause\n* Presence of neurological deficit\n* Inflammatory disease involving the cervical region, such as rheumatoid arthritis\n* Use of muscle relaxant medication within the last 1 week","25 Years",{"count":160,"type":22},120,"This observational study aims to evaluate the prevalence, severity, and characteristics of neck musculoskeletal symptoms among Turkish endodontists. Endodontists are exposed to prolonged static postures and repetitive movements during clinical procedures, which may increase the risk of neck-related disorders.\n\nParticipants will be asked to complete questionnaires regarding demographic characteristics, occupational factors, ergonomic conditions, and neck pain. In addition, physical assessments including cervical range of motion, muscle strength, endurance, posture, and proprioception will be performed using validated measurement tools.\n\nThe study also aims to identify factors associated with neck pain, such as working conditions, posture, and clinical experience. The findings may help improve preventive strategies, ergonomic recommendations, and rehabilitation approaches for dental professionals.",[163,164,165,166,167,168,42,169,170],"Neck Pain","Neck Pain Musculoskeletal","Musculoskeletal Assessment","Musculoskeletal Disorder of the Neck","Musculoskeletal Disorders (MSDs)","Occupational Musculoskeletal Disorders","Endodontics","Dentistry",[172,173,163,100,174,175,103,176,177,96,178,179,180,181,182,183],"Endodontists","Dentists","Cervical Spine","Ergonomics","Neck Disability Index","Posture","Cervical Range of Motion","Musculoskeletal Symptoms","Cervical Isometric Muscle Strength","Neck Muscle Endurance","Cervical Muscle Strength","Forward Head Posture","2026-04-01",{"date":186,"type":74},"2026-04-08",{"date":188,"type":22},"2026-05",{"date":190,"type":22},"2027-08",{"name":192,"class":114},"Atlas University",{"id":194,"slug":195,"hasResults":11,"nctId":196,"briefTitle":197,"officialTitle":198,"acronym":4,"eligibilityCriteria":199,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":200,"targetDuration":4,"studyType":124,"phases":202,"briefSummary":203,"conditions":204,"keywords":207,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":212,"lastUpdatePostDateStruct":213,"startDateStruct":215,"completionDateStruct":217,"leadSponsor":219,"locationsCount":82},"100625045","active-pauses-for-musculoskeletal-disorder-prevention-in-workers-100625045","NCT07417527","Active Pauses for Musculoskeletal Disorder Prevention in Workers","Prevention Program for Musculoskeletal Disorders Through Active Pauses for Workers in the Basque Country","Inclusion Criteria:\n\n* Active workers.\n* Aged 18 years or older.\n* Capability to perform vigorous physical exercise.\n\nExclusion Criteria:\n\n* Medical contraindications to physical exercise.\n* Recent surgery.\n* Pregnancy.",{"count":201,"type":22},150,[126],"The goal of this clinical trial is to learn if short exercise breaks at work can prevent muscle and joint pain in workers. The main questions it aims to answer are:\n\nDo strength exercises help workers move better and feel less pain?\n\nAre strength exercises better than stretching exercises for worker health?\n\nResearchers will compare a strength exercise program to a mobility (stretching) program to see which one works better to improve physical health and work ability.\n\nParticipants will:\n\nPerform short exercise breaks (5 minutes) at their workplace every day for 8 weeks.\n\nAttend one supervised session per week to learn the exercises.\n\nComplete simple physical tests (like standing up from a chair) and answer surveys about their health at the start and end of the study.",[167,42,205,206],"Sedentary Behaviors","Prevention",[208,209,210,211,103],"Active Pauses","Workplace Exercise","Strength Training","Stretching","2026-02-17",{"date":214,"type":74},"2026-02-19",{"date":216,"type":74},"2026-01-01",{"date":218,"type":22},"2029-12",{"name":220,"class":114},"University of the Basque Country (UPV\u002FEHU)",{"id":222,"slug":223,"hasResults":11,"nctId":224,"briefTitle":225,"officialTitle":226,"acronym":227,"eligibilityCriteria":228,"healthyVolunteers":17,"sex":18,"minAge":229,"maxAge":230,"enrollmentInfo":231,"targetDuration":4,"studyType":124,"phases":233,"briefSummary":234,"conditions":235,"keywords":237,"overallStatus":104,"whyStopped":4,"lastUpdateSubmitDate":241,"lastUpdatePostDateStruct":242,"startDateStruct":244,"completionDateStruct":246,"leadSponsor":248,"locationsCount":4},"100592428","arpe-training-for-manual-handling-workers-a-quasi-experimental-study-on-ergonomic-knowledge-and-practice-100592428","NCT06993298","ARPE Training for Manual Handling Workers: A Quasi-Experimental Study on Ergonomic Knowledge and Practice","Development and Effectiveness of the Augmented Reality Physical Ergonomics (ARPE) Training Module for Manual Material Handling Workers: A Quasi-Experimental Study Protocol","ARPE;MMH","Inclusion Criteria:\n\nMalaysian citizen\n\nAge 18 years and above\n\nCurrently employed as a manual material handling (MMH) worker in a warehouse\n\nRegularly performs MMH tasks (e.g., lifting, lowering, pushing, pulling, carrying, holding, or restraining objects weighing 14 kg or more)\n\nWorks a minimum of 8 hours per day in a role involving MMH\n\nOwns a mobile phone capable of downloading and running the MAKAR XR app\n\nExclusion Criteria:\n\nPregnant\n\nCurrently an intern or temporary worker\n\nHas undergone ergonomic training within the past six months","20 Years","60 Years",{"count":232,"type":22},78,[126],"The goal of this study is to evaluate whether an Augmented Reality-based ergonomic training module (ARPE) can improve ergonomic knowledge, self-prevention, and self-evaluation practices among adult manual material handling (MMH) workers in warehouses. The main questions it aims to answer are:\n\nDoes the ARPE training module improve workers' ergonomic knowledge?\n\nDoes it enhance their ability to prevent and assess risks of work-related musculoskeletal disorders (WMSDs)?\n\nResearchers will compare an intervention group using the ARPE module with a control group receiving traditional training based on national ergonomic guidelines to see if the AR module leads to better outcomes.\n\nParticipants will:\n\nAttend a briefing and use the ARPE training via the MAKAR XR app\n\nComplete self-assessment questionnaires at baseline, week 1, and week 6\n\nReceive reminders and follow-ups through WhatsApp",[42,236],"Work Related Upper Limb Disorder",[238,239,240],"Augmented Reality (AR)","Ergonomic","Work Related Musculo skeletal Disorder (WMSD)","2025-05-23",{"date":243,"type":74},"2025-05-28",{"date":245,"type":22},"2025-09-01",{"date":247,"type":22},"2026-10-01",{"name":249,"class":114},"Universiti Teknologi Mara",{"id":251,"slug":252,"hasResults":11,"nctId":253,"briefTitle":254,"officialTitle":254,"acronym":4,"eligibilityCriteria":255,"healthyVolunteers":17,"sex":18,"minAge":158,"maxAge":256,"enrollmentInfo":257,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":259,"conditions":260,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":261,"lastUpdatePostDateStruct":262,"startDateStruct":264,"completionDateStruct":266,"leadSponsor":268,"locationsCount":82},"100580937","the-relationship-between-ergonomic-knowledge-of-healthcare-professionals-and-musculoskeletal-disorders-100580937","NCT06843798","The Relationship Between Ergonomic Knowledge of Healthcare Professionals and Musculoskeletal Disorders","Inclusion Criteria:\n\n* Being between 25 and 45 years old.\n* Being a health worker\n* Having at least 2 years of work experience\n\nExclusion Criteria:\n\n* Participant having a musculoskeletal disorder before the study\n* Having had surgery within 6 months\n* Being pregnant\n* Having a traumatic accident or injury that would affect the study","45 Years",{"count":258,"type":22},400,"This study aims to investigate the relationship between the ergonomic awareness levels of Healthcare Workers and musculoskeletal disorders.",[42],"2025-03-24",{"date":263,"type":74},"2025-03-25",{"date":265,"type":74},"2025-03-15",{"date":267,"type":22},"2025-04-01",{"name":269,"class":114},"Uskudar University",{"id":271,"slug":272,"hasResults":11,"nctId":273,"briefTitle":274,"officialTitle":275,"acronym":276,"eligibilityCriteria":277,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":91,"enrollmentInfo":278,"targetDuration":4,"studyType":124,"phases":280,"briefSummary":281,"conditions":282,"keywords":286,"overallStatus":104,"whyStopped":4,"lastUpdateSubmitDate":296,"lastUpdatePostDateStruct":297,"startDateStruct":299,"completionDateStruct":301,"leadSponsor":303,"locationsCount":4},"100527561","cost-effectiveness-impact-of-a-workplace-based-intervention-to-reduce-occupational-sitting-time-in-office-based-workers-100527561","NCT06149364","Cost-effectiveness, Impact of a Workplace-based Intervention to Reduce Occupational Sitting Time in Office-based Workers","Cost-effectiveness and Impact of a Workplace-based Intervention to Reduce Occupational Sitting Time Among Office-based Workers: a Randomized Controlled Trial","ISKE","Inclusion Criteria:\n\n* working at least six full time hours\n* Age of 18-65 years\n* Speaking Finnish language\n* Having designated access to internet\n* Telephone, and a desk within their workplace (home and away from home workplaces will be considered).\n\nExclusion Criteria:\n\n* Non-ambulatory\n* Pregnant\n* Those participating in other RCTs\n* Those planning relocation",{"count":279,"type":22},140,[126],"The purpose of this study is to examine the impact and cost effectiveness of a workplace-based intervention aimed at reducing prolonged occupational sitting among office-based workers. The study will be conducted in three phases. Phase I: is an Integrative review on economic evaluations of workplace-based interventions for reducing occupational sitting time. Phase II: is a secondary analysis of register data within the Northern Finland Birth Cohort 1966 (NFBC-1966). This is aimed at evaluating the association between prolonged sitting time with societal and\u002For organization economic perspective across different occupational categories at midlife. Phase III will be a Randomized Control Trial (RCT) of an office-based intervention designed to reduce prolonged occupational sitting time. The sample for the RCT will be 140 office-based workers - 70 participants will be enrolled in the control group whilst 70 participants will be enrolled within the intervention group. The study will be conducted from 2021 to 2025. An article-based dissertation will be completed at the end of the study, this will be mainly based on four articles that will be published in international peer reviewed journals.",[283,284,42,285],"Physical Inactivity","Sedentary Behavior","Physical Activity",[287,288,289,290,291,292,293,294,295],"Cost-effectiveness","Economic evaluation","Randomized control trial","Sitting time","Workplace","Office workers","Productivity","Absenteeism","RCT","2024-04-08",{"date":298,"type":74},"2024-04-09",{"date":300,"type":22},"2024-06",{"date":302,"type":22},"2027-12",{"name":304,"class":114},"University of Helsinki"]