Combined exercise and education program to prevent falls in older adults
Effectiveness of Comprehensive Intervention for the Prevention of Fall in Older Adults; a Randomized Controlled Trial
This study tests whether a program that combines exercise and education can help older adults avoid falls better than regular medical care.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 484 (estimated) |
| Ages | 65 Years to 95 Years |
| Sex | All |
| Sponsor | Seoul National University Hospital Academic / other |
| Locations | 1 site (Seoul) |
| Trial ID | NCT05615077 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of a combined exercise and education intervention aimed at reducing fall risk among older adults. It involves a randomized controlled trial comparing this intervention to conventional medical care. Participants will undergo assessments of various physical and cognitive functions at multiple time points over a year, including balance, muscle strength, and quality of life. The goal is to establish a standardized protocol for this combined approach to fall prevention.
Who should consider this trial
Good fit: Ideal candidates are older adults aged 65 to 90 who can walk independently and are willing to participate in a year-long exercise program.
Not a fit: Patients with severe medical conditions, significant neurological deficits, or those requiring assistive devices for mobility may not benefit from this intervention.
Why it matters
Potential benefit: If successful, this intervention could significantly reduce the incidence of falls among older adults, improving their overall health and independence.
How similar studies have performed: Previous studies have shown promising results with combined exercise and education interventions in reducing fall risk, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * patients older than 65 years and under 90 years * if at least one \<3 key question\> is met or \<stay independent score\> ≥ 4 points * patients who can walk more than 10m without an assistive device (ambulatory without an assistive device) * patients who are willing to participate in exercise intervention for 12 months * patients who can receive information about this study, submit written consent before participating in the study, and can comply with the requirements of the clinical trial Exclusion Criteria: * medically unstable conditions (e.g., cirrhosis with complications, end-stage renal failure requiring regular dialysis, hemorrhagic disease, uncontrolled hypertension, those who have been treated for a malignant tumor within 5 years) * in case of ongoing neurological deficit except for stroke survivors (e.g., dementia, Alzheimer's disease, Parkinson's disease, etc.) * decreased cardiopulmonary function such as heart failure, chronic obstructive pulmonary disease * musculoskeletal problems that affect physical function and athletic ability (e.g., those who have undergone hip joint surgery, artificial joint surgery, spine surgery within the last 1 year) * patients who have experienced alcohol abuse within the last 1 year (if 3 or more are meet in Cut off, Annoyed, Guilty, Eye opener \[CAGE\] evaluation) * in case the purpose of this clinical trial cannot be understood or the matters necessary for the study cannot be carried out * when it is judged by other researchers that the subject's condition makes it difficult to participate in this study
Where this trial is running
Seoul
- Seoul National University Hospital — Seoul, South Korea (Recruiting)
Study contacts
- Principal investigator: Keewon Kim, MD, PhD — Seoul National University Hospital
- Study coordinator: Keewon Kim, MD, PhD
- Email: keewonkimm.d@gmail.com
- Phone: +82-10-6238-9649
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.