[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"accidental-falls\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:accidental-falls":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,13,0,[8,49,79,111,140,168,194,221,246,275,299,325,347],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":4},"100636614","tai-chi-intervention-for-balance-function-in-older-adults-predictive-and-modifying-roles-of-circadian-age-100636614",false,"NCT07567976","Tai Chi Intervention for Balance Function in Older Adults: Predictive and Modifying Roles of Circadian Age","Effects of Tai Chi on Balance Function in Community-Dwelling Older Adults: A Randomized Controlled Trial Examining the Predictive and Modifying Roles of Circadian Age, With Multi-Omics and Brain Function Assessments","Inclusion Criteria:\n\n* Aged 55 years or older\n* Community-dwelling\n* Able to walk independently (assistive devices such as canes are permitted)\n* Berg Balance Scale (BBS) score ≤52 at screening\n* Able to understand and follow verbal instructions\n* Willing to wear a wrist accelerometer continuously for 7 days at baseline\n* Willing to accept random group assignment\n* Willing to undergo blood collection during the study\n* Provides written informed consent\n\nExclusion Criteria:\n\n* Regular Tai Chi or yoga practice (more than once per week) within the past 6 months\n* Severe cognitive impairment (Montreal Cognitive Assessment \\[MoCA\\] score \\\u003C20 at screening, or previously diagnosed dementia)\n* Unstable cardiovascular disease (myocardial infarction, stroke, or hospitalization within the past 3 months)\n* Severe musculoskeletal disease that limits exercise participation\n* Neurological diseases affecting balance (e.g., Parkinson's disease, severe peripheral neuropathy)\n* Currently participating in another exercise intervention study\n* Planned surgery or extended absence during the study period\n* Contraindications to functional near-infrared spectroscopy (fNIRS) examination (e.g., scalp injury, metallic implants in the head region)\n* Severe psychiatric illness (e.g., schizophrenia, bipolar disorder)\n* Considered unable to safely participate in moderate-intensity physical activity as judged by the study physician or attending healthcare provider",true,"ALL","55 Years",{"count":20,"type":21},90,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study investigates the effects of a 12-week Tai Chi intervention on balance function in community-dwelling older adults. Participants are randomly assigned to either a Tai Chi exercise group or a health education control group. The primary outcome is balance function measured by the Berg Balance Scale. Secondary outcomes include physical function, psychological well-being, cognitive function, and sleep quality. The study also explores the predictive and modifying roles of baseline circadian age on intervention outcomes.",[27,28,29],"Aging","Postural Balance","Accidental Falls",[31,32,33,34,35,36],"Tai Chi","Tai Ji Quan","Mind-Body Exercise","Older Adults","Fall Prevention","Circadian Rhythm","NOT_YET_RECRUITING","2026-06-30",{"date":40,"type":41},"2026-07-02","ACTUAL",{"date":43,"type":21},"2026-06-01",{"date":45,"type":21},"2027-03",{"name":47,"class":48},"Zhide Liang","OTHER",{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":78},"100561193","occupational-therapy-and-registered-dietitian-services-to-reduce-fall-risk-among-home-delivered-meal-clients-100561193","NCT06586970","Occupational Therapy and Registered Dietitian Services to Reduce Fall Risk Among Home Delivered Meal Clients","Tailored Occupational Therapy and Registered Dietitian Services for Home-Delivered Meal Clients: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Eligible to receive meals according to LifeCare Alliance's standard in-take criteria (Over the age of 60; unable to safely and independently leave the home; does not have access to a caregiver who can prepare meals)\n* Has a working freezer to store between 7-14 frozen meals\u002Fweek\n* Has a working microwave or oven to reheat meals\n* Lives within LifeCare Alliance's 5-county service area\n\nExclusion Criteria:\n\n* Individuals already receiving home-delivered meals from LifeCare Alliance or other meal agency (within the past 40 days)\n* Individuals residing in residential care or a skilled nursing facility\n* Individuals whose dietary restrictions prohibit them from eating meals from LifeCare Alliance's frozen meal selection\n* Individuals at home on hospice care\n* Unable to independently answer LifeCare Alliance's in-take questions","60 Years",{"count":58,"type":21},750,[24],"The purpose of this study is to determine which of the following four service models is most effective for reducing fall risk among home-delivered meal clients: (1) meals alone, (2) meals + registered dietitian services, (3) meals + occupational therapy services, (4) meals + registered dietitian + occupational therapy services.",[62,29,63,64,65,66,67],"Diet, Food and Nutrition","Cardiovascular Diseases","Diabetes","Debility","Frailty","Functional Disability","RECRUITING","2026-04-06",{"date":71,"type":41},"2026-04-13",{"date":73,"type":41},"2024-08-20",{"date":75,"type":21},"2027-07-31",{"name":77,"class":48},"Ohio State University",1,{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":16,"sex":17,"minAge":86,"maxAge":4,"enrollmentInfo":87,"targetDuration":4,"studyType":22,"phases":89,"briefSummary":90,"conditions":91,"keywords":94,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":78},"100567134","development-of-pressure-sensor-based-dementia-and-fall-prevention-program-for-older-adults-100567134","NCT06664229","Development of Pressure Sensor Based Dementia and Fall Prevention Program for Older Adults","Development of the Flexible and Printed Electronic Device for Dementia and Fall Prevention of Older Adults","Inclusion Criteria:\n\n* Older adults in the community who are 65 years old or older.\n\nExclusion Criteria:\n\n* Older adults who cannot walk independently with assisting devices or use wheelchair.\n* Older adults who are diagnosed with dementia, or other neurological\u002Fmental disorders that may limit their cognitive ability to participate in the study.\n* Older adults who cannot speak or read Korean.","65 Years",{"count":88,"type":21},205,[24],"The goal of this intervention program is to test the effectiveness of pressure sensor based dementia and fall prevention program for improving cognitive and physical functions of community dwelling older adults. The main purposes of this study are:\n\n1. Develop a pressure sensor based exercise mat and linked software programs to be used for group training sessions for cognitive and balance training of older adults at a community senior center.\n2. Evaluate efficacy of the program to improve cognitive and physical functions of older adults via a pilot study and a main study with randomized control trial design.\n\nOlder adults will be asked to participate in a group training session that was lead by a fitness coach using a pressure sensor mat, a standing monitor, and a linked software programs. They will be asked to stand on the mat, which is set in front of a monitor to show positions of the mat where they place their foots. The monitor screen will guide them to conduct either a balancing exercise for fall prevention or a cognitive exercise such as memory game or quiz game for dementia prevention.\n\nResearchers will compare age and gender matched control group in a main study to see if cognitive and balancing functions of intervention group is better than the control group by conducting pre and post surveys and physical examinations. A pilot study will examine pre-post changes in the intervention group without the control group.",[92,29,93],"Dementia, Mild","Mild Cognitive Impairment",[95,96,97,98,99,100,101],"Fall prevention","Dementia prevention","Mild cognitive impairment","Exercise game","Cognitive training game","Community based intervention","Older adults","2026-03-17",{"date":104,"type":41},"2026-03-20",{"date":106,"type":41},"2024-01-15",{"date":108,"type":21},"2026-12-31",{"name":110,"class":48},"Sunmi Song",{"id":112,"slug":113,"hasResults":11,"nctId":114,"briefTitle":115,"officialTitle":116,"acronym":4,"eligibilityCriteria":117,"healthyVolunteers":11,"sex":17,"minAge":86,"maxAge":118,"enrollmentInfo":119,"targetDuration":121,"studyType":122,"phases":4,"briefSummary":123,"conditions":124,"keywords":127,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":131,"lastUpdatePostDateStruct":132,"startDateStruct":134,"completionDateStruct":136,"leadSponsor":138,"locationsCount":78},"100626596","fall-prevention-in-older-adults-in-an-italian-cohort-100626596","NCT07437690","Fall Prevention in Older Adults in an Italian Cohort","FALL PREVENTION IN OLDER ADULT: OBSERVATIONAL PROSPECTIVE STUDY ON AN ITALIAN COHORT","Inclusion Criteria\n\nAge ≥ 65 years at the time of enrollment\n\nRadiographically confirmed knee osteoarthritis or hip osteoarthritis classified as Kellgren-Lawrence grade 2 or 3\n\nClinical indication for structured rehabilitation therapy\n\nDiagnosis of sarcopenia according to European Working Group on Sarcopenia in Older People 2 (EWGSOP2) criteria, defined as:\n\nLow muscle strength (handgrip strength \\\u003C 27 kg in men or \\\u003C 16 kg in women, or chair stand test \\> 15 seconds for 5 rises), and\n\nReduced muscle mass confirmed by a validated assessment method (e.g., dual-energy X-ray absorptiometry \\[DXA\\] or bioelectrical impedance analysis \\[BIA\\]) according to established cut-off values\n\nExclusion Criteria\n\nAbsolute contraindication to rehabilitation therapy as determined by the treating physician\n\nHemodynamic instability, including uncontrolled arrhythmias, symptomatic hypotension, or acute coronary syndrome within the previous 3 months\n\nUnstable fractures\n\nSevere open wounds or lacerated-contused injuries requiring surgical management\n\nSevere cognitive impairment preventing participation in rehabilitation activities (e.g., Mini-Mental State Examination score \\\u003C 18)","99 Years",{"count":120,"type":21},50,"2 Months","OBSERVATIONAL","Proximal femoral fractures are associated with increased mortality in older adults and may contribute to loss of functional independence, resulting in a higher risk of long-term institutionalization. The SIOT 2021 guidelines emphasize that management of older patients with proximal femoral fracture (FPF) requires a multidisciplinary approach, ideally integrated across all phases of care, including rehabilitation and secondary prevention at the community level, according to a continuity-of-care model that incorporates the implementation of Fracture Liaison Services.\n\nMultiple clinical, social, and environmental factors influence fall risk. Falls are also associated with psychological consequences. Age-related reductions in muscle strength contribute to progressive functional decline, increased morbidity and mortality related to falls, reduced quality of life, depression, and hospitalization.\n\nSarcopenia is characterized by both quantitative and qualitative reductions in muscle tissue, including progressive replacement of contractile tissue with fibrous and adipose tissue. The European Working Group on Sarcopenia in Older People (EWGSOP), in its updated consensus (EWGSOP2), identifies low muscle strength as the primary parameter of sarcopenia, accompanied by a significant and generalized reduction in muscle mass.\n\nA use-case model dedicated to patients with sarcopenia describes typical demographic and social characteristics, associated comorbidities, and specific care needs, with the aim of identifying the most appropriate management pathways.\n\nThis study adopts a person-centered approach to design, validate, and implement an integrated strategy for fall prevention, taking into account the multiple determinants of fall risk and related adverse health outcomes.",[125,126,29],"Fall Risk, Fall Prevention","Fall Risk",[128,129,130],"accidental falls","sarcopenia","elderly","2026-02-24",{"date":133,"type":41},"2026-02-27",{"date":135,"type":21},"2026-02-20",{"date":137,"type":21},"2026-08-20",{"name":139,"class":48},"Federico II University",{"id":141,"slug":142,"hasResults":11,"nctId":143,"briefTitle":144,"officialTitle":144,"acronym":145,"eligibilityCriteria":146,"healthyVolunteers":16,"sex":17,"minAge":147,"maxAge":4,"enrollmentInfo":148,"targetDuration":150,"studyType":122,"phases":4,"briefSummary":151,"conditions":152,"keywords":153,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":159,"lastUpdatePostDateStruct":160,"startDateStruct":162,"completionDateStruct":164,"leadSponsor":166,"locationsCount":78},"100620279","technology-supported-improvement-management-and-prevention-of-accidental-falls-in-hospitals-100620279","NCT07355556","Technology Supported Improvement, Management and Prevention of Accidental Falls in Hospitals","TechSIMPAFiH","Inclusion Criteria:\n\n* Any member of the ward team as defined by the ward manager including students. All healthcare professional groups, ancillary and administrative staff who work on the selected study ward and any temporary staff from agency or other wards who consent to participate.\n\nExclusion Criteria:\n\n* Any staff under 18 years old","18 Years",{"count":149,"type":21},200,"12 Months","The student will observe fall prevention systems in practice in 2 different hospitals considering how fall prevention technology influences staff behaviour and patients safety in the context of accidental falls in hospital. Accidental falls in hospital are rare but can be life changing for those that suffer them as they are often frail patients who are already vulnerable. Current research shows little improvement with any interventions tested which leaves patient facing clinicians with few resources to assist in the prevention of falls. The investigator believes this is because the measure of accidental falls in hospital is not sensitive enough to calibrate for the different contexts in which patients fall. The student would posit that it is the context that is most influential and addressing the context may lead to improved measures so progress can be made in finding solutions.",[29,35],[154,155,156,157,158],"ethnographic case study","contextual enquiry","observation of clinical staff","The use of technology to prevent falls","mixed methods research","2026-01-12",{"date":161,"type":41},"2026-01-21",{"date":163,"type":21},"2026-04-01",{"date":165,"type":21},"2027-03-31",{"name":167,"class":48},"University of Nottingham",{"id":169,"slug":170,"hasResults":11,"nctId":171,"briefTitle":172,"officialTitle":173,"acronym":4,"eligibilityCriteria":174,"healthyVolunteers":16,"sex":17,"minAge":86,"maxAge":175,"enrollmentInfo":176,"targetDuration":4,"studyType":22,"phases":178,"briefSummary":179,"conditions":180,"keywords":181,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":185,"lastUpdatePostDateStruct":186,"startDateStruct":188,"completionDateStruct":190,"leadSponsor":192,"locationsCount":78},"100495014","a-study-of-dual-task-exercise-training-to-prevent-falls-among-older-adults-with-mild-cognitive-impairment-100495014","NCT05725668","A Study of Dual-task Exercise Training to Prevent Falls Among Older Adults With Mild Cognitive Impairment","Dual-Task Training Exercise to Reduce Falls in Older Adults With Mild Cognitive Impairment","Inclusion Criteria:\n\n* being 65 years and older\n* having complaint of memory loss\n* scoring ≤0.5 on Clinical Dementia Scale\n* having had 1 or more falls in the preceding 12 months or scoring ≥12 seconds on the Timed Up and Go test\n\nExclusion Criteria:\n\n* scoring \\\u003C24 on the Mini-Mental State Examination\n* being able to ambulate independently for household distances\n* having medical clearance\n* having participated in any regular and structured tai ji quan-based exercise programs (≥2 times weekly) in the preceding 6 months\n* having a progressive neuromuscular disorder such as Parkinson's disease or multiple sclerosis\n* being unwilling to be randomized","95 Years",{"count":177,"type":21},336,[24],"To determine the efficacy of a dual-task tai ji quan training therapy in reducing the incidence of falls in older adults with mild cognitive impairment.",[93,29,27],[182,183,184],"Falls","Exercise","Dual tasking","2025-12-09",{"date":187,"type":41},"2025-12-17",{"date":189,"type":41},"2023-07-15",{"date":191,"type":21},"2028-01-31",{"name":193,"class":48},"Oregon Research Institute",{"id":195,"slug":196,"hasResults":11,"nctId":197,"briefTitle":198,"officialTitle":199,"acronym":4,"eligibilityCriteria":200,"healthyVolunteers":16,"sex":17,"minAge":86,"maxAge":4,"enrollmentInfo":201,"targetDuration":4,"studyType":22,"phases":203,"briefSummary":204,"conditions":205,"keywords":208,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":212,"lastUpdatePostDateStruct":213,"startDateStruct":215,"completionDateStruct":217,"leadSponsor":219,"locationsCount":4},"100447544","aquatic-exercise-and-reactive-balance-100447544","NCT05107817","Aquatic Exercise and Reactive Balance","Catching and Throwing Exercises to Improve Reactive Balance: A Randomized Controlled Trial Protocol for the Comparison of Aquatic and Dry-land Training Environments","Inclusion Criteria:\n\n* Ability to stand using a double-leg stance for one minute of time\n* Ability to walk independently\n* Normal or corrected to normal vision\n* Normal or corrected to normal hearing based on a qualitative assessment\n\nExclusion Criteria:\n\n* Any neurological or musculoskeletal disorders that may inhibit the participation in the training and testing protocols\n* A concussion within the past one year before the participation\n* Any cognitive deficiencies (e.g., memory, concentration, or attention disorder)\n* One or more 'yes' answered on the Physical Activity Readiness Questionnaire (PAR-Q)\n* Fear of water",{"count":202,"type":21},44,[24],"The present clinical trial aims to identify if skills acquired during aquatic exercise are more effectively transferred to a reactive balance task than land exercise. This study is designed as a double-blinded, randomized controlled clinical trial. Forty-four older adults aged 60 years or above who meet the eligibility criteria will be recruited and randomized into an aquatic exercise group or land exercise group. Each group will participate in the same balance training exercise during a single session that includes a ball throwing and catching task. A modified lean-and-release test will be implemented on land immediately before, after, and one week after the training session. The outcomes will include reaction time, rapid response accuracy, and mini-BESTest scores obtained from stepping and grasping reactions.",[27,206,29,28,183,207],"Aged","Exercise Therapy",[209,210,211,95],"Reactive balance","Aquatic exercise","Aquatic therapy","2025-04-03",{"date":214,"type":41},"2025-04-08",{"date":216,"type":21},"2026-01",{"date":218,"type":21},"2027-09",{"name":220,"class":48},"Eadric Bressel",{"id":222,"slug":223,"hasResults":11,"nctId":224,"briefTitle":225,"officialTitle":226,"acronym":4,"eligibilityCriteria":227,"healthyVolunteers":16,"sex":17,"minAge":56,"maxAge":4,"enrollmentInfo":228,"targetDuration":4,"studyType":22,"phases":230,"briefSummary":231,"conditions":232,"keywords":236,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":238,"lastUpdatePostDateStruct":239,"startDateStruct":241,"completionDateStruct":243,"leadSponsor":244,"locationsCount":4},"100543969","knee-osteoarthritis-motor-control-risk-of-falls-and-virtual-reality-100543969","NCT06362785","Knee Osteoarthritis, Motor Control, Risk of Falls and Virtual Reality","Study on the Relationship Between Knee Osteoarthritis, Motor Control and the Risk of Falls, and the Effectiveness of Virtual Reality in Managing It in Older People","Inclusion Criteria:\n\n* Age over 60 years.\n* Non-institutionalized individuals.\n* Subjects who wish and consent through informed consent to participate in the study.\n* Have the ability to walk independently (with or without assistive devices).\n* Diagnosis of primary knee osteoarthritis according to the clinical and radiological criteria of the American College of Rheumatology.\n* Specifically, for phase 1, subjects without a knee osteoarthritis diagnosis will also be included.\n\nExclusion Criteria:\n\n* History of significant previous traumas or surgeries to the spine, pelvis, or legs in the last 12 months.\n* Self-reported presence of dizziness, seizures, or epilepsy, aiming to prevent potential exacerbation of symptoms with VR.\n* Vestibular disorders (balance).\n* Neurological diseases, cardiovascular, or respiratory disorders affecting activity; as well as inflammatory or autoimmune diseases affecting the lower limb joints, and other forms of secondary osteoarthritis.\n* Diagnosis of a terminal illness or a health condition that prevents attendance.\n* To have a medical contraindication for exercise.\n* Body Mass Index (BMI) ≥ 40",{"count":229,"type":21},110,[24],"The goal of this clinical trial is to learn about knee osteoarthritis, functionality, and risk of falls in community-dwelling adults aged 60 years and older. The main questions it aims to answer are:\n\n* What are the characteristics of a community-dwelling population over 60 years and older in terms of knee osteoarthritis, functionality, and risk of falls?\n* Does an intervention with virtual reality lower knee osteoarthritis symptoms, raise functionality and prevent falls in community-dwelling adults aged 60 years and older, compared to a control group receiving conventional physiotherapy treatment based on therapeutic exercise?\n\nParticipants will:\n\n* Answer questionnaires.\n* Perform physical laboratory tests through a camera-based motion capture system.\n* Execute task-based exercises in a virtual environment through virtual reality.\n\nResearchers will compare community-dwelling adults aged 60 years and older who execute task based exercises in a virtual environment through virtual reality and community-dwelling adults aged 60 years and older receiving conventional physiotherapy treatment based on therapeutic exercise to see if virtual reality improves knee osteoarthritis symptoms, functionality, and lowers fall risk.",[233,234,29,235],"Knee Osteoarthritis","Task Performance and Analysis","Virtual Reality",[237,234,29,206,235],"Knee osteoarthritis","2025-03-12",{"date":240,"type":41},"2025-03-17",{"date":242,"type":21},"2025-05-01",{"date":43,"type":21},{"name":245,"class":48},"Universidade da Coruña",{"id":247,"slug":248,"hasResults":11,"nctId":249,"briefTitle":250,"officialTitle":251,"acronym":4,"eligibilityCriteria":252,"healthyVolunteers":11,"sex":17,"minAge":253,"maxAge":4,"enrollmentInfo":254,"targetDuration":4,"studyType":22,"phases":256,"briefSummary":257,"conditions":258,"keywords":261,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":266,"lastUpdatePostDateStruct":267,"startDateStruct":269,"completionDateStruct":271,"leadSponsor":273,"locationsCount":78},"100575609","feasibility-of-high-intensity-functional-exercise-with-simultaneous-cognitive-challenge-for-older-people-with-falls-risk-100575609","NCT06774508","Feasibility of High-intensity Functional Exercise with Simultaneous Cognitive Challenge for Older People with Falls Risk","The Feasibility of a High-intensity Functional Exercise Program with Simultaneous Cognitive Challenge to Improve Physical and Cognitive Function in Older People with Intermediate Risk for Falls: a Randomized Controlled Pilot Trial","Inclusion Criteria:\n\n* aged 75 years or older\n* moderate risk of falling (feeling unsteady or afraid of falling, or having fallen in the past year, with a self-selected gait speed ≤0,8 m\u002Fs or TUG \\>15 s without walking aid)\n* can walk independently indoors, without a walking aid\n* can walk 500m independently outdoors, with or without a walking aid\n\nExclusion Criteria:\n\n* a high fall risk (≥2 falls in the past year, serious injury e.g. hip fracture from a fall in the past year requiring medical care, or inability to get up from the floor after a fall)\n* Mini-Mental State Examination (MMSE) score \\\u003C24 or dementia diagnosis\n* a medical condition that may affect participation in high-intensity gait, balance, and leg strength exercise, or other movement-related conditions affecting exercise or tests (e.g., pain, dizziness, visual or hearing impairment)","75 Years",{"count":255,"type":21},33,[24],"This study aims to evaluate the feasibility of a high-intensity functional exercise program with simultaneous cognitive challenge (HIFE+cog) among older people at risk of falls. The evaluation design and intervention development will be assessed with the following specific aims:\n\n1. To investigate the acceptability and safety of the HIFE+cog program in older people at risk of falls, and the methods used in the study by evaluating recruitment, compliance with the intervention, severity of adverse events reported, and participant experiences.\n2. To measure key outcome variables, including completion rates, missing data, estimates, variances, and 95% confidence intervals for between-group differences.\n\nThe study is designed as a randomized controlled pilot trial. Eligible participants will be randomized to either the intervention group (HIFE+cog) or the active control group (HIFE) to partake in individually tailored exercise, supervised and progressed by a physiotherapist, two times per week for 3 months.",[29,28,259,260],"Gait","Cognition",[262,263,259,260,264,265,206],"Accidental falls","Postural balance","Exercise therapy","Resistance training","2025-02-21",{"date":268,"type":41},"2025-02-25",{"date":270,"type":41},"2025-02-17",{"date":272,"type":21},"2025-09-01",{"name":274,"class":48},"Umeå University",{"id":276,"slug":277,"hasResults":11,"nctId":278,"briefTitle":279,"officialTitle":279,"acronym":4,"eligibilityCriteria":280,"healthyVolunteers":16,"sex":17,"minAge":86,"maxAge":281,"enrollmentInfo":282,"targetDuration":4,"studyType":22,"phases":284,"briefSummary":285,"conditions":286,"keywords":287,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":290,"lastUpdatePostDateStruct":291,"startDateStruct":293,"completionDateStruct":295,"leadSponsor":297,"locationsCount":78},"100566654","optimal-intensity-of-reactive-balance-training-for-healthy-older-adults-100566654","NCT06657989","Optimal Intensity of Reactive Balance Training for Healthy Older Adults","Inclusion Criteria:\n\n* Community-dwelling older adults (65-80 years old)\n\nExclusion Criteria:\n\n* Unable to stand independently without upper-limb support for \\>30 seconds and\u002For walk independently (without a gait aid) for ≥10 metres;\n* Diagnosed neurological condition that could affect balance control (e.g., stroke, Parkinson's disease);\n* Score below normative values on the Montreal Cognitive Assessment;\n* Score below age-matched normative values for sensory and motor function, as assessed using the FallScreen battery;\n* Have insufficient English language comprehension such that they cannot understand instructions;\n* Have contraindications to reactive balance training such as severe osteoporosis; and\u002For\n* Are currently attending physiotherapy or supervised exercise.","80 Years",{"count":283,"type":21},96,[24],"Falls in daily life are a serious risk for older adults. A new type of balance training, called reactive balance training (RBT) involves people losing balance many times so that they can practice fast balance reactions, like stepping reactions. Differences in training program features might explain differences in the results of previous RBT studies. Training intensity is the difficulty or challenge of the training program. It would be valuable to know if high-intensity RBT improves balance reactions quickly. The main goal of this study is to see if more intense RBT improves balance reactions faster than less intense RBT. The investigators will compare how quickly people improve balance reactions between high- and moderate-intensity RBT, and between RBT and a control program that does not include RBT. The investigators will also test if the improvements in balance reactions last after the training program is over. The secondary goals are to understand exactly how balance reactions improve with training, and to determine if people who complete RBT improve their general balance skills, and falls efficacy more than people who do not complete RBT.",[29],[263,27,288,289],"Biomechanics","Rehabilitation","2025-01-22",{"date":292,"type":41},"2025-01-27",{"date":294,"type":41},"2025-01-21",{"date":296,"type":21},"2027-12-31",{"name":298,"class":48},"Toronto Rehabilitation Institute",{"id":300,"slug":301,"hasResults":11,"nctId":302,"briefTitle":303,"officialTitle":304,"acronym":4,"eligibilityCriteria":305,"healthyVolunteers":11,"sex":17,"minAge":86,"maxAge":4,"enrollmentInfo":306,"targetDuration":4,"studyType":22,"phases":308,"briefSummary":309,"conditions":310,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":316,"lastUpdatePostDateStruct":317,"startDateStruct":319,"completionDateStruct":321,"leadSponsor":323,"locationsCount":4},"100562467","the-effect-of-digital-education-for-osteoporosis-patients-on-fracture-risk-and-related-health-outcomes-100562467","NCT06603545","The Effect of Digital Education for Osteoporosis Patients on Fracture Risk and Related Health Outcomes.","The Effect of Digital Education for Osteoporosis Patients on Fracture Risk and Related Health Outcomes in Older Swedish Men and Women.","Inclusion Criteria:\n\n* Patients visiting an osteoporosis unit, 65 years and older.\n* Ability to understand and follow study instructions.\n* Signed informed consent.\n* Have been recommended pharmacological osteoporosis treatment after a clinical evaluation including a DXA-scan and assessment of fracture risk at an osteoporosis clinic.\n* Have access to www.1177.se.\n\nExclusion Criteria:\n\n* Patients with previous osteoporosis medication the last year.",{"count":307,"type":21},2640,[24],"A digital education for osteoporosis patients (DEOP) has been developed and tested on patients in Region Vastra Gotaland, Sweden. Currently, the evidence regarding the efficacy of patient education on fracture risk, medication adherence, injurious falls, levels of physical activity, and diet is insufficient. Most patients with osteoporosis in Sweden are diagnosed and treated in primary care, where the knowledge about osteoporosis is often very limited. Thus, in general, osteoporosis patients are not sufficiently informed before receiving a treatment recommendation. This randomized controlled trial aims to investigate if DEOP vs. standard care can reduce the incidence of fracture in older women and men, and if the intervention leads to better adherence to osteoporosis medication, higher quality of life, increased physical activity, and enhanced diet.\n\nThe primary objective is to investigate if DEOP compared to standard care (without DEOP), can reduce the incidence of clinical fractures in men and women, over the age of 65 years, without previous osteoporosis medication the last year, who have been recommended osteoporosis treatment after a DXA scan and assessment of clinical risk factors at an osteoporosis clinic.\n\nThe secondary objectives are to investigate if DEOP compared to standard care (without DEOP), can reduce the incidence of injurious falls, have positive effects on adherence to osteoporosis medication, positively affect diet (calcium and vitamin D intake), physical activity, and improve quality of life in men and women, over the age of 65 years, without previous osteoporosis medication the last year, who have been recommended osteoporosis treatment after a DXA scan and assessment of clinical risk factors at an osteoporosis clinic.\n\nStudy design: randomized multicentre clinical trial. Patients over the age of 65 visiting an osteoporosis unit for a bone density scan (DXA) will be asked to participate in the study. The participants will be randomized to one of two arms where one arm will be invited to DEOP and the other arm will receive standard care, without DEOP.",[311,29,312,313,314,315],"Osteoporosis","Fractures, Bone","Patient Reported Outcome Measures","Drug Adherence","Injury Traumatic","2024-09-16",{"date":318,"type":41},"2024-09-19",{"date":320,"type":21},"2024-09",{"date":322,"type":21},"2029-12",{"name":324,"class":48},"Sahlgrenska University Hospital",{"id":326,"slug":327,"hasResults":11,"nctId":328,"briefTitle":329,"officialTitle":330,"acronym":4,"eligibilityCriteria":331,"healthyVolunteers":16,"sex":17,"minAge":56,"maxAge":281,"enrollmentInfo":332,"targetDuration":4,"studyType":22,"phases":334,"briefSummary":335,"conditions":336,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":337,"lastUpdatePostDateStruct":338,"startDateStruct":340,"completionDateStruct":342,"leadSponsor":344,"locationsCount":4},"100555048","health-education-for-preventing-falls-in-older-adults-living-in-the-community-100555048","NCT06507020","Health Education for Preventing Falls in Older Adults Living in the Community","Health Education for Preventing Falls in Older Adults Living in the Community: a Factorial Randomized Controlled Trial","Inclusion Criteria:\n\n* Age 60-80 inclusive\n* Live in the community\n* Expected to live in their current place of residence for the next 12 months\n* can walk 50 metres without the assistance of an assistive device\n\nExclusion Criteria:\n\n* Exclusion of subjects with acute illness or acute stages of chronic disease",{"count":333,"type":21},888,[24],"This clinical trial aims to evaluate the effectiveness of three health education intervention modules in preventing falls among older adults living in the community. The study is designed as a factorial randomized controlled trial, assessing the impact of three health education intervention modules: Fall prevention knowledge education，Exercise education, and Home hazard reduction education. Each module will have a 'yes' and 'no' version, resulting in eight experimental conditions.\n\nThe primary questions it seeks to address are: (1) What is the main effect of different health education intervention modules on preventing falls in older adults living in the community? (2)What is the interactive effect of different health education intervention modules on preventing falls in older adults living in the community?\n\nThe trial will be conducted in twenty four sub-district in Baiyun District, Guangzhou City. An estimated 37 participants will be recruited from each of the 24 sub-districts, with the sub-districts being randomly assigned to one of the eight experimental groups by a statistician independent of the research team using computer-generated random numbers.",[29,34],"2024-07-16",{"date":339,"type":41},"2024-07-18",{"date":341,"type":21},"2024-08-01",{"date":343,"type":21},"2025-08-01",{"name":345,"class":346},"Guangzhou Center for Disease Control and Prevention","OTHER_GOV",{"id":348,"slug":349,"hasResults":11,"nctId":350,"briefTitle":351,"officialTitle":352,"acronym":353,"eligibilityCriteria":354,"healthyVolunteers":11,"sex":17,"minAge":147,"maxAge":4,"enrollmentInfo":355,"targetDuration":4,"studyType":22,"phases":357,"briefSummary":358,"conditions":359,"keywords":361,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":365,"lastUpdatePostDateStruct":366,"startDateStruct":368,"completionDateStruct":370,"leadSponsor":372,"locationsCount":4},"100539303","the-safety-integration-stakeholders-saints-program-to-integrate-worker-and-patient-safety-in-oregon-rural-hospitals-100539303","NCT06302088","The Safety Integration Stakeholders (SAINTS) Program to Integrate Worker and Patient Safety in Oregon Rural Hospitals","Safety Integration Stakeholders: A Randomized Control Trial to Minimize Patient Fall Risk and Reduce Patient-assist Injuries Among Critical Access Hospital Staff","SAINTS","Inclusion Criteria:\n\n* Employed at participating sites (critical-access hospitals in rural Oregon)\n* Patient-care workers (e.g. RNs, CNAs)\n\nExclusion Criteria:\n\n* Non-clinical staff (e.g. clerical, janitorial)\n* Non-unit staff (e.g. physical therapy)",{"count":356,"type":21},240,[24],"The safety integration stakeholders (saints) program to integrate worker and patient safety in Oregon rural hospitals. The rationale is that the saints program will positively impact outcomes by identifying and training peer leaders on strategies to optimize environmental, administrative, and educational components to become a saint and regularly collaborate with safety stakeholders\u002Fadministrative leaders at each site through continuous improvement cycles (e.g. plan-do-study-act).",[29,360],"Injuries",[362,363,364],"Patient falls","patient-assist injuries","safety climate","2024-03-20",{"date":367,"type":41},"2024-03-22",{"date":369,"type":21},"2024-10-01",{"date":371,"type":21},"2027-12",{"name":373,"class":48},"Oregon Health and Science University"]