[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"disability\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:disability":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,51,76,103,138,174,251,278,303,323],{"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":24,"briefSummary":26,"conditions":27,"keywords":31,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100609919","online-learning-module-to-advance-research-related-to-people-with-disabilities-100609919",false,"NCT07220837","Online Learning Module to Advance Research Related to People With Disabilities","Randomized Control Trial (RCT) of Online Learning Module to Advance Research Related to People With Disabilities (D2\u002FR3)","D2\u002FR3","Inclusion Criteria:\n\n* Aged \\>=18\n* Conducts non-disability focused research (in the past 3 years)\n* Conducts (primarily) research with\u002Fon adults\n* Affirms their understanding that eligibility and data must pass quality assurance checks before compensation is disbursed\n\nExclusion Criteria:\n\n* Participant in Aim1\u002FAim2 of D2\u002FR3 study\n* Respondent fails to provide a valid US-based personal institutional email",true,"ALL","18 Years",{"count":21,"type":22},200,"ESTIMATED","INTERVENTIONAL",[25],"NA","This study will measure the effects of a brief one-time eLearning intervention on researcher Knowledge, Attitudes, and Perceptions (KAP) of including people with disabilities (PWDs) in biomedical \\& behavioral research. Researchers will be recruited from across the Einstein\u002FMontefiore network, and other medical centers with a focus on CTSAs.",[28,29,30],"Developmental Disability","Intellectual Disability","Disability",[32,33,34,35,36,37],"Bias","Attitudes","Perceptions","Inclusion","Translational Science","Representation","RECRUITING","2026-06-17",{"date":41,"type":42},"2026-06-22","ACTUAL",{"date":44,"type":42},"2025-12-16",{"date":46,"type":22},"2026-08",{"name":48,"class":49},"Albert Einstein College of Medicine","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":57,"minAge":58,"maxAge":59,"enrollmentInfo":60,"targetDuration":4,"studyType":23,"phases":62,"briefSummary":63,"conditions":64,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":50},"100640273","comparing-the-effects-of-lumbar-stability-exercises-and-telerehabilitation-on-reducing-lumbar-lordotic-angle-pain-and-disability-in-postpartum-women-100640273","NCT07593183","Comparing the Effects of Lumbar Stability Exercises and Telerehabilitation on Reducing Lumbar Lordotic Angle, Pain, and Disability in Postpartum Women","Inclusion Criteria:\n\n* Female participants 6 weeks up to 12 month post-partum women.\n* Participants who has access to internet services and technologies\n* Participants with mild-to-moderate self-reported low back pain for at least 2 weeks.\n* Objectively measured lumbar lordotic angle beyond normative range of 40 Degree\n\nExclusion Criteria:\n\n* Congenital spine deformities like scoliosis\n* Pelvic prolapsed","FEMALE","20 Years","40 Years",{"count":61,"type":22},38,[25],"Low back pain is the most common symptoms experienced by people throughout the world. Although lifetime prevalence of low back pain among women is more but it is particularly common during pregnancy, affecting approximately 50% of women. Pregnancy induces significant physiological changes, which lead to increased ligamentous laxity that may persist for 3 to 6 months postpartum. Additionally, the expanding uterus shifts the maternal center of gravity anteriorly, resulting in compensatory lumbar hyperlordosis and contributing to lower back discomfort. While these adaptations help accommodate pregnancy, they often do not fully resolve after birth, especially in the presence of abdominal muscle weakness. The result is altered posture characterized by an exaggerated lumbar lordotic curve that may predispose postpartum women to continued pain and lumbar instability. Without a structured postpartum rehabilitation program, these postural abnormalities may go uncorrected. Ensuring adherence and completion of such programs is critical for preventing long-term musculoskeletal complication. There are many efficient way to help in maintaining adherence and completion of program including the use of digital platforms. The increasing availability of low cost internet and communication technologies has enhanced the capacity to deliver healthcare services through internet, enabling broader access to physiotherapy services and follow-up care through telerehabilitation. Telerehabilitation is one of the emerging field of telemedicine, defined as set of tools, procedure, and protocols to deliver the rehabilitation process remotely. The objective of the study is to facilitate implementation of the telerehabilitation for home based program for postpartum female. The objectives of the study is to compare the effectiveness of telerehabilitation-based lumbar stability exercises versus on-site lumbar stability exercises in improving lumbar stability among postpartum female and to facilitate implementation of the telerehabilitation for home based program for postpartum female. It is a randomized controlled trial. Participants meeting the inclusion criteria will be recruited and consent form will be taken than participants will be allocated to group A (On-Site Lumbar Stability exercise) and B (Telerehabilitation) through 1:1 method. Pre-treatment assessment will be carried out on Day 1 using the outcome measures tool like NPRS, ODI and LLA. Participant will receive intervention for 6 weeks, 3 sessions per weeks. After the completion, on 6 week Post-treatment assessment will be carried out using the same outcome measures tool like NPRS, ODI and LLA.",[65,66,30],"Lumbar Lordotic Angle","Lumbar Pain","2026-05-12",{"date":69,"type":42},"2026-05-18",{"date":71,"type":22},"2026-05-13",{"date":73,"type":22},"2026-07-15",{"name":75,"class":49},"Foundation University Islamabad",{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":17,"sex":18,"minAge":83,"maxAge":4,"enrollmentInfo":84,"targetDuration":4,"studyType":23,"phases":86,"briefSummary":87,"conditions":88,"keywords":89,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":94,"lastUpdatePostDateStruct":95,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":50},"100632063","a-digitally-enabled-system-for-precision-assessment-and-intervention-of-disability-risk-in-older-adults-100632063","NCT07508813","A Digitally-Enabled System for Precision Assessment and Intervention of Disability Risk in Older Adults","The Construction of a Digitally-Enabled Precision Assessment and Intervention System for Disability Risk in Older Adults and a Full-Cycle, Multi-Scenario Demonstration Study","Inclusion Criteria:\n\n* Community-dwelling permanent residents aged ≥65 years;\n* Able to operate a smartphone independently or with assistance from a primary caregiver;\n* Clear consciousness with basic comprehension and communication abilities;\n* Voluntarily agree to participate in the study and provide informed consent.\n\nExclusion Criteria:\n\n* Those who are unable to perform basic activities of daily living independently, or who have significant cognitive or communication impairments.","65 Years",{"count":85,"type":22},238,[25],"1. Identify the primary risk factors for disability in older adults through multi-dimensional risk factor screening.\n2. Develop a risk stratification model for disability in older adults by integrating outcome indicators and temporal characteristics, and construct an intelligent early warning model to enable automated assessment and monitoring of disability risk.\n3. Establish key digital technologies for early warning and prevention of disability risk in older adults, and develop a whole-process digital intervention platform incorporating a decision support system for disability prevention management.\n4. Create a digitally empowered hospital-community-household collaborative system for precise assessment and intervention of disability risk in older adults, achieving data-driven whole-process active disability management. The system will be demonstrated and evaluated in communities with diverse characteristics across urban, county, and rural settings.",[30],[90,91,92,93],"older adults","disability","prevention","risk","2026-03-30",{"date":96,"type":42},"2026-04-02",{"date":98,"type":42},"2025-10-31",{"date":100,"type":22},"2026-12-30",{"name":102,"class":49},"Second Affiliated Hospital, School of Medicine, Zhejiang University",{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":109,"eligibilityCriteria":110,"healthyVolunteers":11,"sex":18,"minAge":59,"maxAge":111,"enrollmentInfo":112,"targetDuration":4,"studyType":23,"phases":114,"briefSummary":115,"conditions":116,"keywords":122,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":137},"100611771","therapeutic-effects-of-instrument-assisted-versus-sound-assisted-soft-tissue-mobilization-in-chronic-non-specific-low-back-pain-100611771","NCT07244913","Therapeutic Effects of Instrument-assisted Versus Sound-assisted Soft Tissue Mobilization in Chronic Non-specific Low Back Pain","Therapeutic Effects of Instrument-assisted Versus Sound-assisted Soft Tissue Mobilization Among Patients With Chronic Non-specific Low Back Pain","IASTM VS SASTM","Inclusion Criteria:\n\n* Pain between the inferior gluteal folds and the costal margins.\n* Pain with a duration of a minimum of 24 weeks.\n* Moderate to severe pain (\\>3) was measured using the Numeric Pain Rating Scale.\n* Straight Leg raise Limited (hamstring tightness)\n\nExclusion Criteria:\n\n* Pain in lower back with radiating\u002Freferring but limited to proximal legs\n* Pain for the last 03 months and at least half of the days in the last six months.\n* Presence of neurological problem\u002Fdeficit\u002Fdisease (e.g., nerve root compression, motor deficit, paresthesia) and lower limb symptoms.\n* Presence of disease like Infection, tumors, spondylolisthesis grade II or higher, vertebral fractures, identifiable cause like endometriosis\n* Medicine like immunosuppression or steroid medication;\n* Spinal deformities\n* History of severe rheumatic, orthopedic, or cardiovascular disease in the last three months before study participation.\n* Previously diagnosed Osteoporosis\n* SIJ dysfunction is evaluated by a positive compression test.\n* BMI over 35.\n* Skin allergy or hypersensitivity that can lead to skin irritation due to IASTM\u002FSASTM tools.","55 Years",{"count":113,"type":22},60,[25],"Chronic low back pain (CLBP) is the most common medical problem observed among musculoskeletal pain and spinal pain problems. It can reduce the movements due to muscular imbalances, decreased activity of daily living, and effects on health-related quality of life. It is the major cause of activity limitation, work absence, and reported clinical issues. Most of the cases of low back pain remained undiagnosed and received only symptomatic management.",[117,118,119,120,30,121],"Chronic Non-Specific Low Back Pain","Pelvic Obliquity","Hamstring Flexibility","Physical Function","Lumbar Flexibility",[123,124,125,126,127,118,120,119],"IASTM","SASTM","CPGS","Disability Index","Flexibility","2025-12-30",{"date":130,"type":42},"2026-01-02",{"date":132,"type":42},"2025-12-23",{"date":134,"type":22},"2026-06-04",{"name":136,"class":49},"University of Lahore",2,{"id":139,"slug":140,"hasResults":11,"nctId":141,"briefTitle":142,"officialTitle":143,"acronym":144,"eligibilityCriteria":145,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":146,"targetDuration":4,"studyType":23,"phases":148,"briefSummary":149,"conditions":150,"keywords":153,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":165,"lastUpdatePostDateStruct":166,"startDateStruct":168,"completionDateStruct":170,"leadSponsor":172,"locationsCount":50},"100595859","minnesota-retain-phase-3-100595859","NCT07037927","Minnesota RETAIN Phase 3","Minnesota Retaining Employment and Talent After Injury\u002FIllness Network (RETAIN) Phase 3","MN RETAIN","Inclusion Criteria:\n\n* \\> 18-years-old,\n* MN Resident,\n* Works or intends to work in MN,\n\nMeets one of the following:\n\n* Employed at the time of enrollment (must be a W2 employee) OR,\n* Unemployed and in the workforce (looking for a job) referred by either:\n* Dislocated Worker (DW) Program,\n* Healthcare provider\u002Fcare team managing work restrictions\n* Within 6 months of last day of work,\n\nMeets one of the following:\n\n* Provider work restrictions of unable to work for at least 2 weeks\n* Per healthcare team anticipated to be unable to work for at least 2 weeks\n* Employer's inability to accommodate current work restrictions\n\nMeets one of the following:\n\n* Diagnosis of a personal injury or illness that impacts employment (acute injury\u002Fillness or exacerbation of a chronic condition).\n* Surgery or procedure anticipated within the next 4-weeks that impacts employment\n* Documentation of work restrictions (i.e., written note\u002Fform documentation in electronic medical record prior to enrollment)\n\nExclusion Criteria:\n\n* Does not have the capacity to give appropriate informed consent,\n* Active workers' compensation claim relating to the qualifying injury or illness,\n* Pending application OR Receiving Social Security Disability Insurance (SSDI) or -Supplemental Security Income (SSI),\n* Self-Employed (i.e., 1099 worker)",{"count":147,"type":22},1000,[25],"MN RETAIN Phase 3 is a non-randomized trial to evaluate the impact of RETAIN program expansion and services on workforce retention and reduction of future workplace disability in the state of MN. The program is funded by US Department of Education (DOE). There will be collaboration between partners to implement best practices in early intervention to support injured or ill employees in stay-at-work and return-to-work. MN RETAIN involves a partnership between Mayo Clinic and MN Department of Employment and Economic Development (DEED), and stakeholders throughout MN. MN DEED serves as the main recipient and administrator of the funding within the state with Mayo Clinic a subrecipients of the grant.",[151,152,30],"Injuries Related Work","Illness Related Work",[154,155,144,156,157,158,159,160,161,162,163,164],"RETAIN","Minnesota RETAIN","Illness Recovery","Injury Recovery","Out of work help","Work Placement assistance","Job Help","Work Help","Help Keeping my job","Stay at work","Return to work","2025-10-29",{"date":167,"type":42},"2025-10-30",{"date":169,"type":42},"2025-07-07",{"date":171,"type":22},"2029-09-30",{"name":173,"class":49},"Mayo Clinic",{"id":175,"slug":176,"hasResults":11,"nctId":177,"briefTitle":178,"officialTitle":179,"acronym":180,"eligibilityCriteria":181,"healthyVolunteers":17,"sex":18,"minAge":182,"maxAge":4,"enrollmentInfo":183,"targetDuration":4,"studyType":185,"phases":4,"briefSummary":186,"conditions":187,"keywords":212,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":242,"lastUpdatePostDateStruct":243,"startDateStruct":245,"completionDateStruct":247,"leadSponsor":249,"locationsCount":50},"100469557","generation-victoria-cohort-2020s-a-statewide-longitudinal-cohort-study-of-victorian-children-and-their-parents-100469557","NCT05394363","Generation Victoria Cohort 2020s: A Statewide Longitudinal Cohort Study of Victorian Children and Their Parents","Generation Victoria Cohort 2020s. A Statewide Longitudinal Cohort of Victorian Children and Their Parents","GenV","Inclusion Criteria (Children):\n\n* Birth date between 4th October 2021 and 3rd October 2023\n* Live at the time of recruitment\n* Residing in Victoria at the time of recruitment\n* Has a legally acceptable representative capable of understanding the informed consent document and providing consent on the child's behalf, who provides a signed and dated informed consent form (e.g. a parent\u002Fguardian)\n\nInclusion Criteria (Adults):\n\n* Be a parent or guardian of a child who meets the eligibility criteria above\n* Provide a signed and dated informed consent form or have a legally acceptable representative capable of understanding the informed consent document and providing consent on the participant's behalf.\n\nExclusion criteria:\n\n* Children who are deceased at the time of recruitment (i.e. still born or died after birth) and their parents\u002Fguardians\n* Families unable to provide informed consent in any of the languages available","1 Day",{"count":184,"type":22},150000,"OBSERVATIONAL","Generation Victoria (GenV) is a longitudinal, population-based study of Victorian children and their parents that will bring together data on a wide range of conditions ,exposures and outcomes. GenV blends study-collected, study-enhanced and linked data. It will be multi-purpose, supporting observational, interventional, health services and policy research within the same cohort. It is designed to address physical, mental and social issues experienced during childhood, as well as the antecedents of a wide range of diseases of ageing. It seeks to generate translatable evidence (prediction, prevention, treatments, services) to improve future wellbeing and reduce the future disease burden of children and adults.\n\nThe GenV Cohort 2020s is open to all children born over a two-year period, and their parents, residing in the state of Victoria Australia. The GenV Cohort 2020s is preceded by an Advance Cohort of children born between 5 Dec 2020 and 3 October 2021, and their parents. This comprises all families recruited at GenV's Vanguard hospital (Joan Kirner Women's and Children's) and at birthing hospitals throughout Victoria as GenV scaled up to commence recruiting for the GenV Cohort 2020s. The Advance Cohort have ongoing and full participation in GenV for their lifetime unless they withdraw but may have less complete data and biosamples.",[188,189,190,191,192,193,194,195,196,197,198,199,200,201,202,30,203,204,205,206,207,208,209,210,211],"Mental Health","Child Wellbeing","Infant Health","Child Health","Reproductive Health","Healthy Aging","Health Equity","Quality of Life","Social Determinants of Health","Environmental Exposure","Genetics","Cognition","Learning","Child Development","Congenital Abnormalities","Injuries","Communicable Diseases","Noncommunicable Diseases","Physical Fitness","Diet","Obesity","Allergy and Immunology","Inflammation","Intergenerational Relations",[213,180,214,215,216,191,217,218,219,220,221,222,223,224,225,226,227,228,229,230,231,232,194,233,234,235,236,237,238,239,196,240,241],"Generation Victoria","Cohort Studies","Data Collection","Data Linkage","Midlife Health","Children","Infants","Family","Parents","Mothers","Fathers","Life course perspective","Population Health","Longitudinal Studies","Genetics, population","Demography","Epidemiology","Health Disparity","Minority Health","Vulnerable Populations","Clinical Trial","Randomized Controlled Trial","Pragmatic Clinical Trial","Health Services Research","Economic Models","Value of Life","Geographic Information Systems","Climate Change","Built Environment","2025-07-30",{"date":244,"type":42},"2025-08-03",{"date":246,"type":42},"2021-10-04",{"date":248,"type":22},"2033-10",{"name":250,"class":49},"Murdoch Childrens Research Institute",{"id":252,"slug":253,"hasResults":11,"nctId":254,"briefTitle":255,"officialTitle":255,"acronym":256,"eligibilityCriteria":257,"healthyVolunteers":17,"sex":18,"minAge":83,"maxAge":4,"enrollmentInfo":258,"targetDuration":4,"studyType":185,"phases":4,"briefSummary":260,"conditions":261,"keywords":266,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":269,"lastUpdatePostDateStruct":270,"startDateStruct":272,"completionDateStruct":274,"leadSponsor":276,"locationsCount":50},"100582470","the-beijing-longitudinal-disability-survey-in-community-elderly-100582470","NCT06863727","The Beijing Longitudinal Disability Survey in Community Elderly","BLINDSCE","Inclusion Criteria:\n\n* Community-dwelling adults aged 65 years or older who reside in Beijing.\n* Participants who sign an institutionally approved informed consent.\n\nExclusion Criteria:\n\n* Participants with severe mental disorders and serious medical conditions preventing study investigation\n* Participants undergoing long-term professional treatment for physical function and cognitive functioning, such as hospitalization or rehabilitation.",{"count":259,"type":22},1962,"The goal of this observational study is to establish the prospective cohort of the Beijing Longitudinal Disability Survey in Community Elderly (BLINDSCE) to explore the high-risk factors and preventive interventions for disability and cognitive impairment among community-dwelling adults aged 65 years and over. The main question it aims to answer is:\n\n* What are the high-risk factors able to predict the incidence and advance of disability and cognitive impairment in community-dwelling adults aged 65 years and over?\n* What are the categories of function and cognitive performance trajectory in community-dwelling adults aged 65 years and over?",[262,30,263,264,265],"Ageing","Cognitive Impairment","Frailty","Intrinsic Capacity",[262,30,263,267,268],"Community","Cohort","2025-03-03",{"date":271,"type":42},"2025-03-07",{"date":273,"type":42},"2023-08-07",{"date":275,"type":22},"2028-07-31",{"name":277,"class":49},"Xuanwu Hospital, Beijing",{"id":279,"slug":280,"hasResults":11,"nctId":281,"briefTitle":282,"officialTitle":282,"acronym":283,"eligibilityCriteria":284,"healthyVolunteers":17,"sex":18,"minAge":285,"maxAge":4,"enrollmentInfo":286,"targetDuration":4,"studyType":185,"phases":4,"briefSummary":288,"conditions":289,"keywords":293,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":295,"lastUpdatePostDateStruct":296,"startDateStruct":298,"completionDateStruct":300,"leadSponsor":302,"locationsCount":50},"100552406","china-healthy-aging-cohort-study-100552406","NCT06472674","China Healthy Aging Cohort Study","China-Ageing","Inclusion Criteria:\n\n* Aged 60 years or older\n* Lived in the community for more than 1 year\n* Signed the informed consent form\n\nExclusion Criteria:\n\n* Cannot complete the survey","60 Years",{"count":287,"type":22},6780,"This is a community-based prospective cohort study in China. The study has been initialized in 2024 and included older residents. The goal of this observational study is to explore the risk factors related to disability and dementia in the elderly Chinese community population, and develop a risk prediction model for disability and dementia.",[290,30,291,292],"Age Problem","Dementia","Death",[294],"Disability, Dementia, Ageing, Cohort","2024-06-23",{"date":297,"type":42},"2024-06-25",{"date":299,"type":42},"2024-06-13",{"date":301,"type":22},"2063-06",{"name":277,"class":49},{"id":304,"slug":305,"hasResults":11,"nctId":306,"briefTitle":307,"officialTitle":307,"acronym":308,"eligibilityCriteria":284,"healthyVolunteers":17,"sex":18,"minAge":285,"maxAge":4,"enrollmentInfo":309,"targetDuration":4,"studyType":185,"phases":4,"briefSummary":311,"conditions":312,"keywords":313,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":315,"lastUpdatePostDateStruct":316,"startDateStruct":318,"completionDateStruct":320,"leadSponsor":322,"locationsCount":50},"100546429","beijing-disability-risk-and-ageing-monitoring-study-100546429","NCT06394817","Beijing Disability Risk and Ageing Monitoring Study","BEAM",{"count":310,"type":22},2000,"This is a community-based prospective cohort study in Beijing, China. The study has been initialized in 2023 and enrolled older residents. This study aims to develop disability risk assessment standards and an early warning model for older adults.",[290,30,292],[314],"Disability, Ageing, Cohort","2024-06-17",{"date":317,"type":42},"2024-06-20",{"date":319,"type":42},"2023-02-20",{"date":321,"type":22},"2063-05",{"name":277,"class":49},{"id":324,"slug":325,"hasResults":11,"nctId":326,"briefTitle":327,"officialTitle":328,"acronym":329,"eligibilityCriteria":330,"healthyVolunteers":11,"sex":18,"minAge":331,"maxAge":332,"enrollmentInfo":333,"targetDuration":4,"studyType":23,"phases":335,"briefSummary":336,"conditions":337,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":340,"lastUpdatePostDateStruct":341,"startDateStruct":343,"completionDateStruct":345,"leadSponsor":347,"locationsCount":50},"100502352","orofacial-functions-and-masticatory-function-in-children-with-different-types-of-deterioration-in-oral-health-100502352","NCT05821140","Orofacial Functions and Masticatory Function in Children With Different Types of Deterioration in Oral Health","Evolution of the Maturation of Orofacial Functions and of the Masticatory Function During a Rehabilitation Program, in Children With Different Types of Deterioration in Oral Health","KIDYCROC","Inclusion Criteria:\n\n* All children, from 3 to 17 years old (inclusion limits), attending the special dental care unit of the CHU Estaing in Clermont Ferrand or the CH Guy Thomas in Riom are included in the study:\n* Children and adolescents who have given their consent (6-17 years) and whose legal guardians have given their consent.\n* Children (3-6 years old) with consent from the legal guardian.\n* The subject is affiliated with a Social Security system.\n\nThis may include:\n\n1. children with multiple caries, requiring full rehabilitation under sedation or general anesthesia +\u002F- prosthetic rehabilitation,\n2. children with orofacial dysmorphologies\u002Fmalocclusions, associated or not with a general syndrome, requiring orthodontic and\u002For prosthetic treatment\n3. children with dental abnormalities, associated or not with a general syndrome, requiring conservative, orthodontic and\u002For prosthetic treatment,\n4. children with a healthy oral status in the course of their bi-annual oral health chek-up.\n\nExclusion criteria:\n\n* Children with an ASA III or IV category according to the American Society of Anesthesiologists\n* Children who do not have a solid diet due to severe neuromotor disorders.\n* Children for whom a geographical or organizational barrier prevents follow-up in the service, children in social placement\n* Children over 18 years of age\n* Children (6-17 years) who do not volunteer to participate\n* Children (6-17 years old) who are unable to give consent to participate in the research.\n* Children for whom one of the legal guardians refuses to participate in the study\n* Children whose legal guardians are not capable of giving informed consent.\n* Children who are not affiliated to a Social Security system.\n* Pregnant or nursing teenagers","3 Years","17 Years",{"count":334,"type":22},112,[25],"This project aims at studying the evolution of masticatory function (food bolus granulometry, masticatory behavior, muscle activity and masticatory performance) during oral rehabilitation, in children with different types of oral health impairment.\n\nSecondary objectives are to study the relationships between children masticatory function (food bolus granulometry, masticatory behavior, muscle activity and masticatory performance) and its evolution during oral rehabilitation, and:\n\n* their type of oral health alteration\n* their eating behaviors\n* their height and weight status\n\nDuring examination the following parameters are collected:\n\n* Various clinical indicators of oral health\n* The child's weight and height\n* Frequency and nature of orofacial dysfunctions\n* The oral health related quality of life of children and their families\n* Chewing tests are performed (chewing gum, natural food such as carrot, cereals, and cheese samples, samples of gelatins of different hardness)\n\nExamination and differents tests are performed every six months for a total of 5 years (per participant)\n\nThe dental care procedures performed during the study were carried out in the usual way.",[338,30,339,201],"Mastication","Oral Stage","2023-04-06",{"date":342,"type":42},"2023-04-20",{"date":344,"type":42},"2022-07-05",{"date":346,"type":22},"2032-02",{"name":348,"class":49},"University Hospital, Clermont-Ferrand"]