Effectiveness of an Automated Falls-Risk Screening and Referral Tool in the Emergency Department (ED)

February 13, 2026 updated by: University of Wisconsin, Madison

Preventing Future Falls in Older Adult ED Patients: Evaluating the Implementation and Effectiveness of a Novel Automated Screening and Referral Intervention - Assessing Outcomes From Medical Records and Medicare Claims Data

The purpose of this retrospective cohort study is to evaluate the effectiveness of an EHR-based clinical decision support system (CDS) for automatically screening older adult ED patients for risk of future falls and providing ED clinicians opportunity to place referrals orders to the UW Health Mobility and Falls Clinic for those at highest risk prior to discharge.

This CDS tool has already been implemented at the UW Hospital ED, and as a QI initiative will be implemented in a staged process at two other UW Health-affiliated emergency departments (The American Center and Swedish American Hospital).

Study Overview

Status

Recruiting

Conditions

Detailed Description

The specific aim of this retrospective cohort study is to test the effectiveness of the automated screening and referral intervention on completed referrals to the UW Health fall prevention clinic and rates of injurious falls, using a limited dataset created from EHR and Medicare claims data. The investigators hypothesize that ED patients referred using the falls risk CDS tool will have decreased healthcare use due to fall-related injuries, and that the intervention will have similar levels of effectiveness across different types of patient characteristics. The investigators will also systematically examine barriers to patients completing their clinic referrals, as well as clinic scheduling and pre-visit planning protocols that may have excluded patients from receiving Falls Clinic services.

Effectiveness will be assessed based on examination of a limited dataset consisting of EHR and Medicare claims data measuring rates of (1) patient referrals at each ED, (2) completed referrals to the Mobility and Falls Clinic (i.e., a completed clinic appointment), and (3) healthcare visits for fall-related causes occurring within the six months following the initial ED visit.

The primary analysis to evaluate effectiveness of the fall-risk CDS tool will include data from older adult patients (age ≥65) who visit study EDs during the intervention period at each site, have a UW Health System-affiliated primary care provider, and are discharged from the ED or ED observation unit (not admitted). Members of the UWH Applied Data Science team (not part of the study team) will extract data from patient EHR to create a limited dataset including: past falls and fall-related injuries (in the 12 months pre-visit, including the index ED visit), post-visit falls and fall-related injuries (in the 6 months following the index ED visit), patient demographics (age, gender, race/ethnicity, insurance), comorbidities, active medications, and utilization (e.g., primary and specialty care visits). Education and income levels will be approximated using census track data. Area Deprivation Index will also be employed based on patient address. These variables will be extracted retrospectively and stored on secure servers.

Study Type

Observational

Enrollment (Estimated)

30000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Illinois
      • Rockford, Illinois, United States, 61008
        • Not yet recruiting
        • Swedish American Emergency Department
    • Wisconsin
      • Madison, Wisconsin, United States, 53718
        • Recruiting
        • East Madison Hospital
      • Madison, Wisconsin, United States, 53792
        • Recruiting
        • UWHC Emergency Department

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

ED patients age 65 or older who are not admitted.

Description

Retrospective analysis will include data from:

  • ED patients 65 years or older
  • discharged from the ED (not admitted)

Study Plan

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

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Discharged ED Patients prior to Intervention
Patients aged 65 and older who are in the emergency department and subsequently discharged (not admitted)
Discharged ED Patients after Intervention
Patients aged 65 and older who are in the emergency department and subsequently discharged (not admitted)
CDS in the Electronic Health Record (EHR) to screen patients at high-risk for future falls enabling referrals to the UW Health Mobility and Falls clinic.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of Falls and Fall-Related Injuries
Time Frame: during the period 12 months prior to ED visit to 6 months post ED visit (18 month period)
Comparison of data before and after implementation of CDS tool and before and after ED visit.
during the period 12 months prior to ED visit to 6 months post ED visit (18 month period)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Summary of Reasons Patients Did Not Schedule or Attend Appointments Based on Referral
Time Frame: during the period 12 months prior to ED visit to 6 months post ED visit (18 month period)
Implementation outcome
during the period 12 months prior to ED visit to 6 months post ED visit (18 month period)
Percentage of Referred Patients Reached by Clinic Scheduler
Time Frame: during the period 12 months prior to ED visit to 6 months post ED visit (18 month period)
during the period 12 months prior to ED visit to 6 months post ED visit (18 month period)
Percentage of Referred Patients Who Made Clinic Appointments
Time Frame: during the period 12 months prior to ED visit to 6 months post ED visit (18 month period)
during the period 12 months prior to ED visit to 6 months post ED visit (18 month period)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Brian W Patterson, MD, MPH, University of Wisconsin, Madison

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 22, 2022

Primary Completion (Estimated)

August 1, 2026

Study Completion (Estimated)

August 1, 2026

Study Registration Dates

First Submitted

March 30, 2023

First Submitted That Met QC Criteria

March 30, 2023

First Posted (Actual)

April 12, 2023

Study Record Updates

Last Update Posted (Actual)

February 17, 2026

Last Update Submitted That Met QC Criteria

February 13, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • 2021-0776
  • SMPH/EMERG MED (Other Identifier: UW Madison)
  • 1K08HS024558 (U.S. AHRQ Grant/Contract)
  • 1R18HS027735 (U.S. AHRQ Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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