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Clinical Trials/NCT05606328
NCT05606328
Completed
N/A

Improving Delirium Screening and Detection for Older Adults Presenting to the Emergency Department (ED): A Novel ED Delirium Screening and Detection Program

Northwell Health1 site in 1 country18 target enrollmentFebruary 28, 2023

Overview

Phase
N/A
Intervention
Emergency Department Delirium Screening and Detection Program (ED-DDP)
Conditions
Delirium
Sponsor
Northwell Health
Enrollment
18
Locations
1
Primary Endpoint
Accurate Delirium Screening by Emergency Department (ED) Nurses (RE-AIM: Efficacy)
Status
Completed
Last Updated
3 months ago

Overview

Brief Summary

Delirium occurs in up to 20% of older adults presenting to the Emergency Department (ED) and is associated with poor outcomes. Failure to identify patients with ED delirium not only prevents initiation of mitigation strategies, but is also a barrier to advancing the field in terms of evaluating management and clinical outcomes. This project studies the potential of an ED Delirium Detection Program (ED-DDP), developed to address the need for consistent and accurate ED delirium detection.

This research will have two objectives:

  • Aim 1 will conduct a pilot stepped wedge cluster randomized trial (SW-CRT) of the ED-DDP across 3 diverse EDs to determine preliminary efficacy of the detection training program, and
  • Aim 2 will use a mixed methods approach to assess RE-AIM implementation outcomes (Reach, Efficacy, Adoption, Implementation, and Maintenance) of the training program.

Aim 1 will consist of a multicomponent 1-day delirium champion workshop where the training is delivered, real-time direct observation/training of champions via telehealth, practical training of nurses throughout each ED by champions, and patient chart review. In Aim 2, the investigators will assess implementation outcomes using training logs, tele-observation, interviews with champions and nurses, and electronic medical record screening.

The overarching aim of this proposal is to determine the preliminary efficacy of the training program for improving ED delirium screening, detection, and management in older adults, while also evaluating implementation outcomes of the program for champions/nurses. The investigators will use findings from this study to inform a full-scale SW-CRT to evaluate the impact of the program on patient outcomes at Northwell Health. The long-term goal of this study is to implement and disseminate a comprehensive ED-DDP that will improve screening, detection, and management of ED delirium in older adults.

Detailed Description

Grounded in the RE-AIM framework, investigators will use mixed methods to conduct implementation outcome assessments of the ED-DDP for champions and nurses. A multimodal approach, using training logs, tele-observations, and EHR data, will assess quantitative outcomes during implementation/intervention periods: Reach (training completion), Efficacy (accurate screening tool use), Adoption (screening rates), and Implementation (fidelity/time of program delivery). Investigators will conduct semi-structured interviews (intervention period) to assess and explain: successes and challenges of training completion (Reach) and Adoption of delirium screening; adaptations made to ED DDP delivery (Implementation); and plan for Maintenance.

Registry
clinicaltrials.gov
Start Date
February 28, 2023
End Date
October 8, 2024
Last Updated
3 months ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Nurse educators, managers, or bedside nurses self-identified or recommended by emergency department (ED) leadership to volunteer as a program site champion
  • Primarily working at a participating ED site
  • Commitment to program participation

Exclusion Criteria

  • Unable to meet program requirements, including attending champion workshop, agreement to observation and training via telehealth, and commitment to train department staff
  • Does not primarily work in the ED

Arms & Interventions

Implementation Period

ED leadership at each site will identify 5-10 delirium champions (nurse educators and managers, bedside nurses) based on their interest in delirium and commitment to program participation, including training of nurses by champions. The implementation period will take place over a period of 3 months. No data analysis will take place during the implementation period.

Intervention: Emergency Department Delirium Screening and Detection Program (ED-DDP)

Intervention Period

The intervention period will take place 3-9 months after implementation of the ED-DDP program over a 15 month period, depending on when a site is randomized to receive the ED-DDP intervention.

Outcomes

Primary Outcomes

Accurate Delirium Screening by Emergency Department (ED) Nurses (RE-AIM: Efficacy)

Time Frame: Intervention period (3-9 months post program implementation)

Tele-observations will be used to asses screening accuracy, defined as the proportion of nurses who score at least 80% accuracy on the brief confusion assessment method (bCAM) use using a validated Spot Check Form. The investigators will observe a random sample of nurses (N=30, 10 at each ED site) performing a delirium screen in real-time. A successful outcome will be considered if computed proportion of nurses accurately using the bCAM tool is 80% or higher.

Secondary Outcomes

  • Proportion of Delirium Champions Who Complete Training (RE:AIM: Reach)(Implementation period (3 months))
  • Proportion of Emergency Department Nurses Who Complete Training (RE-AIM: Reach)(Implementation period (3 months))
  • Proportion of Nurses Who Screen Eligible Patients (REAIM: Adoption)(Intervention period (3-9 months post implementation))
  • Proportion of Training Program Components That Adhered to ED-DDP Protocol (REAIM: Implementation/Fidelity)(Implementation period (3 months))
  • Time Required to Train Delirium Champions and Nurses (REAIM: Implementation/Time)(Implementation period (3 months))

Study Sites (1)

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