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

Sponsor
University of Wisconsin, Madison (Other)
Overall Status
Recruiting
CT.gov ID
NCT05810064
Collaborator
Agency for Healthcare Research and Quality (AHRQ) (U.S. Fed)
300,000
3
53.3
100000
1877.7

Study Details

Study Description

Brief Summary

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).

Condition or Disease Intervention/Treatment Phase
  • Other: Falls-Risk Clinical Decision Support (CDS) Tool

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 Design

Study Type:
Observational
Anticipated Enrollment :
300000 participants
Observational Model:
Other
Time Perspective:
Retrospective
Official Title:
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
Actual Study Start Date :
Feb 22, 2022
Anticipated Primary Completion Date :
Aug 1, 2026
Anticipated Study Completion Date :
Aug 1, 2026

Arms and Interventions

Arm 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)

Other: Falls-Risk Clinical Decision Support (CDS) Tool
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.

Outcome Measures

Primary Outcome Measures

  1. Number of Falls and Fall-Related Injuries [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.

Secondary Outcome Measures

  1. Summary of Reasons Patients Did Not Schedule or Attend Appointments Based on Referral [during the period 12 months prior to ED visit to 6 months post ED visit (18 month period)]

    Implementation outcome

  2. Percentage of Referred Patients Reached by Clinic Scheduler [during the period 12 months prior to ED visit to 6 months post ED visit (18 month period)]

  3. Percentage of Referred Patients Who Made Clinic Appointments [during the period 12 months prior to ED visit to 6 months post ED visit (18 month period)]

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Retrospective analysis will include data from:
  • ED patients 65 years or older

  • discharged from the ED (not admitted)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Swedish American Emergency Department Rockford Illinois United States 61008
2 East Madison Hospital Madison Wisconsin United States 53718
3 UWHC Emergency Department Madison Wisconsin United States 53792

Sponsors and Collaborators

  • University of Wisconsin, Madison
  • Agency for Healthcare Research and Quality (AHRQ)

Investigators

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

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Wisconsin, Madison
ClinicalTrials.gov Identifier:
NCT05810064
Other Study ID Numbers:
  • 2021-0776
  • 1K08HS024558
  • 1R18HS027735
  • SMPH/EMERG MED
First Posted:
Apr 12, 2023
Last Update Posted:
Apr 13, 2023
Last Verified:
Apr 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Apr 13, 2023