Skip to content

Transforming nursing assessment in acute hospitals: A cluster randomised controlled trial of Evidence-based Nursing CORE assessment (the ENCORE trial)

Effectiveness of an evidence-based nursing core assessment protocol in general wards on patient, staff and economic outcomes: A cluster randomised controlled trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12618001903279
Acronym
The ENCORE Trial
Enrollment
32247
Registered
2018-11-22
Start date
2019-09-01
Completion date
2020-06-30
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The rising acuity and complexity of hospital care has increased the need for patient surveillance while also posing obstacles to this practice in general wards. Nursing assessment practices are narrow, focused on vital signs and concentrated at the pointy end of actual patient deterioration: a stage at which effective and preventative nursing intervention is not relevant and medical rescue is the model of care. This three year single blind, cluster-randomised controlled trial will be implemented across seven hospitals. It will test an enhanced model of nurse surveillance, supported by systems-level practice change, redirecting practice from rescue to prevention of patient deterioration in general wards. The project provides the first rigorous evaluation of strengthening nurse surveillance to improve patient and organisational outcomes, including studies of clinical and cost effectiveness.

Interventions

The ENCORE intervention is a complex systems intervention. Each intervention ward will adopt the following core components of the intervention: Proactive surveillance: A structured Core Plus nursing surveillance model for recognition of early changes in patient status on general wards. *Core assessment comprises standardised minimum assessment activities that are common across all clinical areas. The Plus specialty assessment parameters are customised minimum assessment activities relevant to

The ENCORE intervention is a complex systems intervention. Each intervention ward will adopt the following core components of the intervention: Proactive surveillance: A structured Core Plus nursing surveillance model for recognition of early changes in patient status on general wards. *Core assessment comprises standardised minimum assessment activities that are common across all clinical areas. The Plus specialty assessment parameters are customised minimum assessment activities relevant to the ward specialty areas. *The Core Plus model is designed for collection and synthesis of patient data to inform further symptom directed assessment and/or ongoing care decisions. ENCORE informs nursing care planning and multidisciplinary team communication. Systems re-design: Facilitated ward-level practice change to embed the Core Plus model and optimise early intervention for preventable deterioration. *Nurses will conduct Core Plus assessment of patients in their allocation at the beginning of each shift. *The patient’s primary nurse reviews patient status and goals of care during multidisciplinary team ward rounds. Our partner investigators are committed to support ward-level negotiated and tailored strategies to enable and sustain this practice change and embed the ENCORE intervention in ward routine. In re-focusing nursing assessment practices from minimal vital signs recording to purposeful assessment, the ENCORE intervention will strengthen nurse surveillance to ensure adequate and ongoing monitoring of acute care patients’ health status. This practice model will optimise nurses’ capacity to detect and act on emerging indicators of a change in patient status, enabling early intervention for preventable deterioration and adverse events. A 6-month implementation period for intervention wards will support staff engagement and participation in developing context-specific solutions for practice change: *Implementation will adopt an external-internal model of facilitation. Expert external facilitators (research team) will work with internal facilitators (ENCORE leads) on each intervention ward to embed practice change. Each intervention ward will contribute ENCORE leads (clinical nurses) for 6 months as internal facilitators responsible for their ward’s implementation plan, supported by the project coordinator/research team. *Ward staff (targeting >80% of permanent registered nurses in each ward) will attend face-to-face, group-based introductory (1 x 4 hours) and development (1 x 2 hours) ENCORE workshops over the first month of implementation, facilitated by the project coordinator/research team. Workshops are designed to be collaborative and participatory in customising the Core Plus assessment model and developing local strategies for ward-level practice change. *Clinical reminders and ENCORE intervention resources will be provided on each intervention ward (i.e. a video demonstrating the core components of the intervention, posters, lanyard-sized cards, Core Plus assessment bedside guidelines, professional stethoscopes for nurses). Sponsorship for the study was sought from the Executive Directors of Nursing and Chief Executive Officers of each hospital prior to the funding application. A prospective process evaluation will examine implementation outcomes of the ENCORE intervention including uptake, fidelity, acceptability and sustainability. This will be achieved using surveys, focus group and individual interviews of clinical staff participants conducted by a member of the research team.

Sponsors

Queensland University of Technology
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used) (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Clusters: Eligible hospital wards (clusters) will be general acute care wards, between 20-30 beds and where >70% of nursing staff are permanent (full or part time). Patients: Patients will be recruited prospectively from all hospitals using identical tools and methods, six months following commencement of the intervention allowing embedding of the intervention into routine care. All eligible patients admitted to participating wards over a six month period will be recruited using an opt-out approach for access to medical records. Eligible patients will be 18 years and over and screened by ward nursing staff as able to read and understand the plain language study information provided on admission. Nursing and Medical Staff: All nurses who work as permanent staff in the participating wards and medical officers in those wards will be invited to participate in a survey at baseline, 6 months and 12 months post intervention.

Exclusion criteria

Specialist acute care units (e.g., ICU, Coronary Care Unit, Operating Theatres) will be ineligible to participate.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 7, 2026