Actively Recruiting

Age: 18Years - 100Years
All Genders
ID06997328

5 Rs to Rescue A Cluster Trial With an Embedded Process Evaluation

Led by University of Cape Town · Updated on 2026-01-23

6000

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Failure to rescue refers to preventable deaths after surgery due to delays in identifying and treating complications. This research aims to evaluate whether a quality improvement intervention called '5 Rs to Rescue' can enhance monitoring and care for surgical patients in hospitals across four African countries: Ethiopia, South Africa, Tanzania, and Uganda. The study uses a multi-center, cluster trial design with mixed methods to assess the intervention's impact on reducing postoperative deaths. The '5 Rs to Rescue' intervention focuses on five key areas: assessing risk with the ASOS risk score, recognizing patient deterioration through regular vital signs and an Early Warning Score system, responding promptly using care pathways for common complications, reassessing patients after deterioration, and reflecting on care during regular meetings. This complex intervention is implemented in participating hospitals to improve patient surveillance after surgery. Participants are adults aged 18 and older who have surgery and receive postoperative care on study wards. Researchers will monitor the effectiveness of the intervention by reporting site-specific findings related to reducing in-hospital deaths within 72 hours after surgery. The study includes process evaluations and ongoing reflections to understand how the program works in practice. Participation involves routine monitoring and data collection during the postoperative period, with study completion expected by September 2026.

CONDITIONS

Brief Title

'5 Rs to Rescue' A Cluster Trial With an Embedded Process Evaluation

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years and older undergoing any surgery
  • Patients who will receive postoperative care on a participating ward
Not Eligible

You will not qualify if you...

  • Patients who opt out of trial participation
  • Patients receiving end of life care

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

Duration - Up to 72 hours after surgery

Participants who undergo routine surgical care and postoperative monitoring are observed to evaluate the impact of the '5 Rs to Rescue' quality improvement intervention on patient outcomes after surgery.

Continuous monitoring during postoperative care

Trial Site Locations

Total: 1 location

1

Groote Schuur Hospital

Cape Town, Western Cape, South Africa, 7808

Actively Recruiting

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Research Team

M

Margot Flint, PhD

B

Bruce Biccard, MBChB; PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

Perioperative patient outcomes in the African Surgical Outcomes Study: a 7-day prospective observational cohort study.

Bruce M Biccard, Thandinkosi E Madiba, Hyla-Louise Kluyts...

https://pubmed.ncbi.nlm.nih.gov/29306587

Enhanced postoperative surveillance versus standard of care to reduce mortality among adult surgical patients in Africa (ASOS-2): a cluster-randomised controlled trial.

ASOS-2 Investigators

https://pubmed.ncbi.nlm.nih.gov/34418380