NCT07028463 · University of Colorado, Denver
ALERT-ED: Awareness and Linkage to Resources for At-Risk Emergency Department Patients
(ALERT-ED)
What this study is about
Falls are the leading reason for injury-related emergency department (ED) visits in older adults with high rates of ED revisits for falls. Evidence-based fall prevention programs can reduce falls by 30%, but older adults commonly describe limited awareness of resources.
View original scientific description
Falls are the leading reason for injury-related emergency department (ED) visits in older adults with high rates of ED revisits for falls. Evidence-based fall prevention programs can reduce falls by 30%, but older adults commonly describe limited awareness of resources. Currently, all UCHealth ED patients receive fall risk screening on ED arrival, but patients are rarely made aware of their screening results or referred to resources. To address this gap, our team developed ALERT-ED, an intervention where study patients receive automated notification of fall risk screening results and referral via Livi to evidence-based fall prevention programs near their homes. If ALERT-ED is successful, we will demonstrate that UCHealth can improve patient health via pragmatic, automated notification of screening results and referral to resources. Although we designed ALERT-ED to intervene on fall risk in EDs, the intervention could be used for other health concerns central to UCHealth's mission including for patients seeking care for transplants, cancer, brain health, or orthopedic concerns.
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- 65 years or older
- Screens high risk falls on the Geriatric Fall assessment tool (as shown in protocol and used as standard practice in study ED)
Exclusion criteria
- Does not consent to follow up interview
Where
- Aurora, Colorado
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced May 1, 2026 · Source of record for eligibility and locations