Understanding corridor care in UK emergency departments

ISRCTN ISRCTN16396025
DOI https://doi.org/10.1186/ISRCTN16396025
IRAS number 343816
Secondary identifying numbers CPMS 65013
Submission date
10/01/2025
Registration date
09/05/2025
Last edited
09/05/2025
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Other
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Background and study aims
Crowding in emergency departments leads to patient care in areas not originally designed for this use, known as “escalation areas”. This includes repurposed clinical areas and non-clinical areas, such as hospital corridors. A standardised definition of this umbrella term is yet to be generated. To date, there is no evidence describing how many patients are cared for in such environments, who these patients are and any effect on longer-term outcomes for patients with this experience. This study aims to address these evidence gaps by:
1. Defining emergency department escalation areas
2. Estimating the number of patients cared for in escalation areas
3. Describing which patients experience escalation area care
The results will evidence the scale of crowding in UK emergency departments and help to inform policy debate about resource allocation to emergency care. It will also support future research into the effect of escalation area care on patient outcomes.

Who can participate?
Patients presenting to the emergency department who spend some or all of their stay in an escalation area or who are admitted to hospital without spending time in an escalation area.

What does the study involve?
The study involves no change to the tests carried out or treatment received. It involves the collection of information that is recorded as part of the routine care provided to the relevant patients.

What are the possible benefits and risks of participating?
There is no anticipated benefit to individual patients taking part in this study. There is the potential for future benefit to participants and other healthcare users if the findings are used to inform the future use of escalation areas and how care is delivered in these areas. As there is no change to tests or treatment as part of the study, and all information used is recorded as part of routine clinical care, there is no additional risk to participants in terms of the care they receive. There are small privacy and confidentiality risks that are addressed in the manner in which data is collected and stored

Where is the study run from?
The study is sponsored by North Bristol NHS Trust (UK). It is led by the UK Royal College of Emergency Medicine (RCEM) Trainee Emergency Research Network (TERN). The chief investigator for the study is based at the University of Bristol (UK)

When is the study starting and how long is it expected to run for?
March 2024 to May 2025

Who is funding the study?
The Royal College of Emergency Medicine (UK)

Who is the main contact?
Dr Ben Clarke (TERN Fellow), tern@rcem.ac.uk

Study website

Contact information

Dr Tom Roberts
Public, Scientific, Principal Investigator

University of Bristol
Bristol
BS8 1QU
United Kingdom

ORCiD logoORCID ID 0000-0003-4991-974X
Email tom.roberts@bristol.ac.uk

Study information

Study designMulti-centre observational cohort study with a combination of prospective and retrospective recruitment
Primary study designObservational
Secondary study designDelphi study
Study setting(s)Hospital
Study typeSafety
Participant information sheet Not available in web format, please use contact details to request a participant information sheet
Scientific titleUnderstanding escalation area and corridor care in UK emergency departments: an observational cohort and Delphi study
Study acronymUnCorKED
Study objectivesWhat proportion of Emergency Department patients are being cared for in escalation areas and who are they?
Ethics approval(s)

Approved 01/12/2024, London - Brighton & Sussex Research Ethics Committee (2 Redman Place, London, E20 1JQ, United Kingdom; +44 (0)2071048202; brightonandsussex.rec@hra.nhs.uk), ref: 24/LO/0837

Health condition(s) or problem(s) studiedUK Emergency Department use of escalation areas
InterventionMulticentre observational cohort study utilising a 'snapshot' approach to identify the proportion of patients within UK emergency departments who are being looked after in the escalation area. Data will be collected at the departmental and individual patient levels.

The potential cohort for this study is all patients in the ED at each of the five snapshots. These snapshots will be spread out over a 2-week period (with at least 48 hours between timepoints) from 3rd to 16th March 2025. From this cohort, any patient who spends any time in an escalation area OR does not spend any time in an escalation area and subsequently is deemed to require admission to hospital will be included in the study. This is a purely observational study so there is no change to any patient's management. The researchers will complete follow-up data collection in up to 28 days.
Intervention typeOther
Primary outcome measureThe proportion of patients in UK Emergency Departments having care provided in escalation areas, prospectively collected at sites, performed at each of the five snapshots spread out over a 2-week period (with at least 48 hours between timepoints) from 3rd to 16th March 2025
Secondary outcome measures1. Demographics of patients within UK Emergency Departments who are being looked after in escalation areas, collected from the electronic health record for each eligible patient at each snapshot
2. 28-day hospital length of stay and mortality rates for patients who receive care in escalation areas, collected from the electronic health record for each eligible patient at each snapshot
3. Type of escalation area(s) experienced, collected from the electronic health record for each eligible patient at each snapshot
4. Time spent in escalation areas, collected from the electronic health record for each eligible patient at each snapshot
5. ED diagnosis, collected from the electronic health record for each eligible patient at each snapshot
6. ED disposition, collected from the electronic health record for each eligible patient at each snapshot

These five snapshots will be spread out over a 2-week period (with at least 48 hours between timepoints) from 3rd to 16th March 2025
Overall study start date28/03/2024
Completion date31/05/2025

Eligibility

Participant type(s)Patient
Age groupAll
SexBoth
Target number of participants10000
Key inclusion criteriaAny patient present in the ED at the recruitment time points, who experience ED escalation area care during their ED stay or are admitted to hospital. Escalation areas will be defined for the purposes of identifying eligible patients as any area not routinely used unless the capacity of the usual ED geographical footprint is exceeded.
Key exclusion criteriaDoes not meet the inclusion criteria
Date of first enrolment03/03/2025
Date of final enrolment16/03/2025

Locations

Countries of recruitment

  • England
  • Northern Ireland
  • Scotland
  • United Kingdom
  • Wales

Study participating centres

Airedale NHS Foundation Trust
Airedale General Hospital
Skipton Road
Steeton
Keighley
BD20 6TD
United Kingdom
The Grange University Hospital
Caerleon Road
Cwmbran
NP44 8YN
United Kingdom
Southmead Hospital
Southmead Road
Westbury-on-trym
Bristol
BS10 5NB
United Kingdom

Sponsor information

North Bristol NHS Trust
Hospital/treatment centre

Research & Development
North Bristol NHS Trust
Level 3, Learning & Research Building
Southmead Hospital
Westbury-on-Trym
Bristol
BS10 5NB
England
United Kingdom

Phone +44 (0)117 4149330
Email research@nbt.nhs.uk
Website http://www.nbt.nhs.uk/
ROR logo "ROR" https://ror.org/036x6gt55

Funders

Funder type

University/education

Royal College of Emergency Medicine
Private sector organisation / Universities (academic only)
Alternative name(s)
RCEM
Location
United Kingdom

Results and Publications

Intention to publish date03/03/2026
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryData sharing statement to be made available at a later date
Publication and dissemination planThe results of this study will be submitted for publication in an appropriate peer reviewed journal. They will be presented at emergency care focussed conferences. In addition to this they will be disseminated by social media and the TERN website.
IPD sharing planThe data-sharing plans for the current study are unknown and will be made available at a later date

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Protocol file version 6.0 10/02/2025 28/03/2025 No No

Additional files

46672_PROTOCOL_V6.0_10Feb25.pdf

Editorial Notes

13/01/2025: Study's existence confirmed by the HRA.