Accidental Falls

17

Review clinical trials related to Accidental Falls. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Optimal Intensity of Reactive Balance Training for Healthy Older Adults

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.

Participants needed: 96
Trial details
Age: 65-80Biological sex: AllType: InterventionalSponsor: Toronto Rehabilitation InstituteUpdated: Sep 29, 2026Locations: 1
Eligibility criteria

Community-dwelling older adults (65-80 years old)

Unable to stand independently without upper-limb support for >30 seconds and/or... [+6]

Status: Not yet recruiting

Effect of Otago vs. Sensorimotor Training on Balance and Fall Risk in People With Diabetes

The purpose of this study is to compare the effects of the Otago Exercise Program versus Sensorimotor Training on dynamic postural stability and risk of fall in patients with type 2 diabetes mellitus. Participants will be randomly assigned into two equal intervention groups. One group will receive the Otago Exercise Program, while the other group will receive Sensorimotor Training. Both groups will participate in their respective exercise protocols for 8 weeks. Dynamic postural stability and the risk of falling will be assessed before and after the intervention period using standardized physical therapy evaluation tools.

Participants needed: 40
Trial details
Age: 45-55Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Oct 2, 2026
Eligibility criteria

Diagnosed with type 2 diabetes mellitus for at least 5 years. [+6]

Severe diabetic complications (e.g., advanced neuropathy with complete loss of p... [+8]

Status: Not yet recruiting

A Manualized Recreational Therapy Balance Program for Older Adults With Parkinson's and Movement Disorders

This study evaluates a manualized recreational therapy balance program for older adults with Parkinson's disease and movement disorders who live in small cities and rural areas of Oklahoma, where access to movement disorder specialists is limited. Twenty-four older adults with Parkinson's disease and movement disorders will be randomly assigned to one of two groups of 12. One group will attend the balance program continuously for 24 weeks. The other group will attend the program for 12 weeks and will then be observed for 12 weeks without the program. All sessions are led by a Certified Therapeutic Recreation Specialist and last about 50 minutes once a week. Participants will be assessed three times: before the program begins, at three months, and at six months. The assessments measure gait velocity and stride length, postural stability, fall-related confidence, anxiety and depression, and social connectedness. The purpose of the study is to learn how long a community balance program needs to continue for older adults to keep the gains they make, and how quickly those gains decline when the program ends.

Participants needed: 24
Trial details
Age: 50+Biological sex: AllType: InterventionalSponsor: Oklahoma State UniversityUpdated: Sep 29, 2026Locations: 1
Eligibility criteria

Diagnosis of Parkinson's disease or another movement disorder [+3]

Medical condition that prevents safe participation in balance exercise [+1]

Status: Recruiting

Comparative Effects of Reactive Balance Training and Task-Oriented Training on Postural Stability in Patients With Diabetic Peripheral Neuropathy

Diabetic peripheral neuropathy (DPN) is a common complication of prolonged hyperglycemia that damages peripheral nerves, leading to impaired sensory function, increased fall risk, and reduced quality of life. Balance training has shown promising effects in improving postural stability and reducing fall risk in individuals with DPN by engaging visual, vestibular, and proprioceptive systems and promoting central nervous system adaptation. This randomized controlled trial aims to compare the effects of Reactive Balance Training (RBT) and Task-Oriented Training (TOT) on postural stability in patients with DPN. The study will be a single-blinded, two-group randomized controlled trial conducted over one year at Foundation University College of Physical Therapy. A sample of 36 participants will be recruited through convenience sampling and randomly allocated into two groups using the coin-toss method. Ethical approval will be obtained from the FUSH ERC, and written informed consent will be obtained after explaining the study procedures, risks, and benefits. Postural stability will be assessed using the Posture Assessment Checklist, Mini-BESTest, Functional Reach Test (FRT), and Timed Up and Go (TUG). Group A will receive RBT, while Group B will receive TOT. Each session will last 30-40 minutes, including a 5-7-minute warm-up, 20-30 minutes of group-specific intervention, and a 5-minute cool-down. Participants will receive 60-second rest intervals after every three sets or 8-10 repetitions. The intervention will continue for six weeks, with three sessions per week, totaling 18 sessions. Assessments will be conducted at baseline, at week 3, and post-intervention at week 6 using the same outcome measures.

Participants needed: 36
Trial details
Age: 40+Biological sex: AllType: InterventionalSponsor: Foundation University IslamabadUpdated: Sep 18, 2026Locations: 1
Eligibility criteria

Both gender [+6]

History of neurological disorders other than DPN (e.g., stroke, Parkinson's dise... [+4]

Status: Not yet recruiting

Polymodal Fall Prediction in Healthy Older Adults: Clinical, Laboratory, and Blood-Based Biomarkers

The goal of this observational study is to identify clinical, laboratory, and biological markers associated with past (and future falls) in healthy older adults aged 65 years and over. The main question it aims to answer is: Which clinical, functional, laboratory, and blood-based markers distinguish older adults who have fallen at least once during the previous 12 months from those who have not? Researchers will compare older adults with a history of falls with similar older adults without a history of falls. One hundred healthy older adults aged 65 and over, including both fallers and non-fallers, will be recruited for the study. Participants will complete questionnaires and undergo cognitive and physical tests, physical activity and sleep monitoring, gait, balance, muscle, sensory and vestibular assessments, brain and muscle imaging, and blood sampling. Blood samples will be used to study proteins and genetic variants that may be associated with falls. Participants will then be followed for one year using a smartphone-based application to report falls. The study is based on the hypothesis that a history of falling in an otherwise healthy older adult may be associated with subtle clinical, functional, and biological differences compared with a similar older adult without a history of falls. The findings may support the future development of more accurate and scalable tools for early fall-risk detection and targeted fall-prevention strategies. No direct therapeutic benefit is expected from participation.

Participants needed: 100
Trial details
Age: 65+Biological sex: AllType: ObservationalSponsor: Slb PharmaUpdated: Sep 4, 2026
Eligibility criteria

being aged ≥65 years, [+5]

neurological or psychiatric disorders affecting motor or cognitive function (e.g... [+8]

Status: Recruiting

The Effects of Light-Targeted Balance Training on Balance, Functional Performance, and Fear of Falling in Individuals With a History of Falls

In recent years, exercise programs based on visual stimuli have been reported to improve balance and motor control . However, studies investigating the effects of light-targeted balance training on balance, functional performance, and fear of falling in individuals with a history of falls are limited. The aim of this study is to determine the effects of light-targeted balance training on balance, functional performance, and fear of falling in individuals with a history of falls. In addition, the study aims to investigate whether this training method provides additional benefits compared with traditional balance training. The findings of this study are expected to contribute to the development of rehabilitation programs aimed at preventing falls.

Participants needed: 50
Trial details
Age: 18-95Biological sex: AllType: InterventionalSponsor: Uskudar UniversityUpdated: Aug 31, 2026Locations: 1
Eligibility criteria

History of at least one fall within the past 12 months [+4]

Acute orthopedic injury or an active musculoskeletal condition causing pain [+5]

Status: Not yet recruiting

Tai Chi Intervention for Balance Function in Older Adults: Predictive and Modifying Roles of Circadian Age

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.

Participants needed: 90
Trial details
Age: 55+Biological sex: AllType: InterventionalSponsor: Zhide LiangUpdated: Jul 2, 2026
Eligibility criteria

Aged 55 years or older [+8]

Regular Tai Chi or yoga practice (more than once per week) within the past 6 mon... [+9]

Status: Recruiting

Occupational Therapy and Registered Dietitian Services to Reduce Fall Risk Among Home Delivered Meal Clients

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.

Participants needed: 750
Trial details
Age: 60+Biological sex: AllType: InterventionalSponsor: Ohio State UniversityUpdated: Apr 13, 2026Locations: 1
Eligibility criteria

Eligible to receive meals according to LifeCare Alliance's standard in-take crit... [+3]

Individuals already receiving home-delivered meals from LifeCare Alliance or oth... [+4]

Status: Recruiting

Development of Pressure Sensor Based Dementia and Fall Prevention Program for Older Adults

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: 1. 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. 2. 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. Older 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. Researchers 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.

Participants needed: 205
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Sunmi SongUpdated: Mar 20, 2026Locations: 1
Eligibility criteria

Older adults in the community who are 65 years old or older.

Older adults who cannot walk independently with assisting devices or use wheelch... [+2]

Status: Not yet recruiting

Fall Prevention in Older Adults in an Italian Cohort

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. Multiple 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. Sarcopenia 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. A 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. This 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.

Participants needed: 50
Trial details
Age: 65-99Biological sex: AllType: ObservationalSponsor: Federico II UniversityUpdated: Feb 27, 2026Locations: 1Duration: 2 Months
Eligibility criteria

Not listed

Status: Not yet recruiting

Technology Supported Improvement, Management and Prevention of Accidental Falls in Hospitals

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.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of NottinghamUpdated: Jan 21, 2026Locations: 1Duration: 12 Months
Eligibility criteria

Any member of the ward team as defined by the ward manager including students. A...

Any staff under 18 years old

Status: Recruiting

A Study of Dual-task Exercise Training to Prevent Falls Among Older Adults With Mild Cognitive Impairment

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.

Participants needed: 336
Trial details
Age: 65-95Biological sex: AllType: InterventionalSponsor: Oregon Research InstituteUpdated: Dec 17, 2025Locations: 1
Eligibility criteria

being 65 years and older [+3]

scoring <24 on the Mini-Mental State Examination [+5]

Status: Not yet recruiting

Aquatic Exercise and Reactive Balance

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.

Participants needed: 44
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Eadric BresselUpdated: Apr 8, 2025
Eligibility criteria

Ability to stand using a double-leg stance for one minute of time [+3]

Any neurological or musculoskeletal disorders that may inhibit the participation... [+4]

Status: Not yet recruiting

Knee Osteoarthritis, Motor Control, Risk of Falls and Virtual Reality

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: * What are the characteristics of a community-dwelling population over 60 years and older in terms of knee osteoarthritis, functionality, and risk of falls? * 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? Participants will: * Answer questionnaires. * Perform physical laboratory tests through a camera-based motion capture system. * Execute task-based exercises in a virtual environment through virtual reality. Researchers 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.

Participants needed: 110
Trial details
Age: 60+Biological sex: AllType: InterventionalSponsor: Universidade da CoruñaUpdated: Mar 17, 2025
Eligibility criteria

Age over 60 years. [+5]

History of significant previous traumas or surgeries to the spine, pelvis, or le... [+6]

Status: Not yet recruiting

The Effect of Digital Education for Osteoporosis Patients on Fracture Risk and Related Health Outcomes.

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. The 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. The 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. Study 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.

Participants needed: 2,640
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Sahlgrenska University HospitalUpdated: Sep 19, 2024
Eligibility criteria

Patients visiting an osteoporosis unit, 65 years and older. [+4]

Patients with previous osteoporosis medication the last year.

Status: Not yet recruiting

Health Education for Preventing Falls in Older Adults Living in the Community

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. The 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? The 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.

Participants needed: 888
Trial details
Age: 60-80Biological sex: AllType: InterventionalSponsor: Guangzhou Center for Disease Control and PreventionUpdated: Jul 18, 2024
Eligibility criteria

Age 60-80 inclusive [+3]

Exclusion of subjects with acute illness or acute stages of chronic disease

Status: Not yet recruiting

The Safety Integration Stakeholders (SAINTS) Program to Integrate Worker and Patient Safety in Oregon Rural Hospitals

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/administrative leaders at each site through continuous improvement cycles (e.g. plan-do-study-act).

Participants needed: 240
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Oregon Health and Science UniversityUpdated: Mar 22, 2024
Eligibility criteria

Employed at participating sites (critical-access hospitals in rural Oregon) [+1]

Non-clinical staff (e.g. clerical, janitorial) [+1]