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Rescue for Emergency Surgery Patients Observed to uNdergo Acute Deterioration

RESPOND Study (Rescue for Emergency Surgery Patients Observed to uNdergo Acute Deterioration)

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04919720
Acronym
RESPOND
Enrollment
9064
Registered
2021-06-09
Start date
2021-03-05
Completion date
2026-02-28
Last updated
2021-06-09

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

Conditions

Emergencies, Failure to Rescue

Keywords

Emergency General Surgery, Safety II, Human Factors and Ergonomics, Failure to Rescue, Laparotomy

Brief summary

This is a Five Year programme designed to identify and evaluate human factors interventions to improve the response to patients deteriorating following emergency surgery. The programme comprises four work packages: Work Package 1: Qualitative interviews and observations to analyse current rescue systems; Work Package 2: Identify and co-design interventions to improve rescue systems,involving both staff and patients and carers; Work Package 3: Mixed-methods feasibility trial across 3 sites in England, Work Package 4: Step-wedge randomised control trial based across 24 hospital sites in England, evaluating efficacy of interventions in improving response to deteriorating patients.

Detailed description

Patient safety researchers study problems in healthcare systems which harm patients. The investigators wish to study a healthcare situation where system problems are costing lives. In Emergency General Surgery (EGS), dealing mainly with patients with severe abdominal pain, the death rate after abdominal surgery to find out what's wrong (called 'laparotomy') is 5 times higher than for similar routine surgery. Studies of serious complications after major operations show that when patients deteriorate after surgery, their chances of survival depend on how quickly and how well clinical teams react. The investigators plan to analyse how EGS teams currently treat deteriorating patients, and help them develop and test better response systems. Up to 3000 deaths per year could be avoided if these systems were improved . Human Factors science analyses how complex work systems succeed or fail, and how to improve them. The investigators will conduct a Human Factors analysis of real life responses to deterioration in EGS laparotomy patients, examining how staff actually deal with deteriorating patients (referred to as work as done), and how this differs from official guidelines (referred to as work as imagined). A modern approach to Human Factors called Safety II studies both strengths and weaknesses of systems to design solutions. The investigators will use this method to analyse current EGS rescue systems, and develop a new system for managing deterioration, including ways of involving patients or carers effectively. The investigators will test and modify this system until it can be shown that it improves team performance during rescue. Once it appears stable and effective, the investigators will test it in a multi-hospital trial. Hospitals will start using the new system at different dates (decided by chance), and the investigators will compare their performance before and after they start. The investigators will study the cost-effectiveness of the intervention and analyse what worked well and why, to make sure the lessons are learned effectively.

Interventions

BEHAVIORALFRAM Model and Human Factors/Quality Improvement Intervention

The group will use semi-structured interviews and ethnographic observations to inform development of a Functional Resonance Analysis Method (FRAM) model of the process for rescue of deteriorating patients in EGS, using information from 3 hospitals. A focus group approach will be used in co-designing reform of the system for responding to post-operative deterioration, working with small groups of frontline clinical staff from relevant areas in the three Trusts involved.

Sponsors

Oxford University Hospitals NHS Trust
CollaboratorOTHER
University of Michigan
CollaboratorOTHER
University of Southern California
CollaboratorOTHER
University of Leicester
CollaboratorOTHER
University of Birmingham
CollaboratorOTHER
Jonkoping University
CollaboratorOTHER
LP Human Factors Ltd
CollaboratorUNKNOWN
Chelsea and Westminster NHS Foundation Trust
CollaboratorOTHER
HUMAN FACTORS EVERYWHERE
CollaboratorUNKNOWN
University of Oxford
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Step-wedge, cluster-randomised trial

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Senior Medical staff in EGS and in other departments and disciplines with important roles in rescue (Anaesthetics, Gastroenterology, Interventional Radiology, Intensive Treatment Unit) * Junior medical staff in EGS (First Year 1 and 2, Core trainee and Surgical Trainee 3 + grades) * Senior nursing staff in EGS and other relevant departments (Theatres, Intensive Treatment Unit/outreach) * Recovered patients or their carers

Exclusion criteria

* Patients lacking mental capacity * Patients who cannot communicate in English AND for whom translation facilities cannot be secured * Patients with documented PTSD (Post Traumatic Stress Disorder) related to their experience of complications after laparotomy

Design outcomes

Primary

MeasureTime frameDescription
Improvement in response to deterioration12 monthsReduction in ratio of mortality to complications
Improved Effectiveness of response to deterioration12 monthsNumber, severity and duration of Modified Early Warning Score (MEWS) system alerts,
Improved quality of response to deterioration12 monthsQualitative interview data with senior surgeons showing comparison of response quality and success in cases where patient or carer alerts were present with those where they were not
Improved effectiveness of response to deterioration12 monthsNumber of specialist interventions following emergency laparotomy

Secondary

MeasureTime frameDescription
Improvement in mortality of emergency laparotomy patients12 monthsreduction in mortality of emergency laparotomy patients
Improvement in recovery of emergency laparotomy patients12 monthsReduction in ITU stay and overall hospital stay

Countries

United Kingdom

Contacts

Primary ContactPeter McCulloch, MBChB, MD
mcculloch.pa@nds.ox.ac.uk07786267510
Backup ContactElena Villarreal
elena.villarreal@nds.ox.ac.uk

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026