Recruiting soon

ALERT-EDEmergency Department Patients At-Risk Awareness & Resources Linkage Program

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Study Aim

This study aims to increase awareness and resources for emergency department patients who are at risk of falling, with the goal of reducing fall-related emergency department visits.

What is being tested

ALERT-ED

Behavioral
Who is being recruted

Emergencies+1

+ Pathologic Processes

+ Pathological Conditions, Signs and Symptoms

Over 65 Years
+3 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Prevention Study

Interventional
Study Start: December 2025
See protocol details

Summary

Principal SponsorUniversity of Colorado, Denver
Study ContactElizabeth M Goldberg, MD, ScMMore contacts
Last updated: December 11, 2025
Sourced from a government-validated database.Claim as a partner

Study start date: December 1, 2025

Actual date on which the first participant was enrolled.

Falls are a major cause of injuries in older adults, often leading to repeated visits to the emergency department. Many older adults are not aware of fall prevention resources that can help reduce their risk of falls by up to 30%. Currently, patients at UCHealth emergency departments are screened for fall risk, but they rarely learn about their results or get directed to helpful resources. This study introduces ALERT-ED, a program designed to automatically notify patients of their fall risk screening results and refer them to nearby fall prevention programs. If successful, this could significantly improve patient health by making it easier for them to access necessary resources, and the approach could be applied to other health concerns such as transplant care or cancer. Participants in this study will receive an automated message about their risk of falls as soon as they arrive at the emergency department. This message will also include a referral to local fall prevention programs, which are based on proven methods to help reduce the occurrence of falls. The study will evaluate how effective this notification and referral system is in connecting patients with the resources they need. By making this process automated, it aims to ensure that more patients are informed about their health and can take action to prevent future falls, ultimately improving their quality of life.

Official TitleALERT-ED: Awareness and Linkage to Resources for At-Risk Emergency Department Patients 
Principal SponsorUniversity of Colorado, Denver
Study ContactElizabeth M Goldberg, MD, ScMMore contacts
Last updated: December 11, 2025
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

20700 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Prevention Study

Prevention studies aim to stop a disease from developing. They often involve people at risk and test things like vaccines, lifestyle changes, or preventive medications.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 65 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

EmergenciesPathologic ProcessesPathological Conditions, Signs and SymptomsDisease Attributes

Criteria

2 inclusion criteria required to participate
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)

1 exclusion criteria prevent from participating
Does not consent to follow up interview

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Patient receives link to the Livi Chatbot in After Visit Summary

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

UCHealth

Aurora, United StatesSee the location
Recruiting soonOne Study Center