ClinicalTrials.gg
Status unknownNCT02069028Updated Feb 21, 2014

Effectiveness of Different Interventions for Implementing Surviving Sepsis Campaign (SSC) Guidelines on Compliance and Mortality: Systematic Review and Meta-analysis

An observational study in Sepsis, Septic and Septicemia, sponsored by King Abdullah International Medical Research Center. Status unknown. Per ClinicalTrials.gov, last updated 2014-02-21.

Sponsored by King Abdullah International Medical Research Center · Observational

The sponsor has not verified this record recently (last verified Feb 2014), so the status shown — last known as Active, not recruiting — may be out of date.
Study type
Observational
Enrollment
30
Sex
All
01

Study summary

This is a systematic review and Meta-Analysis of interventions for implementation of Surviving Sepsis Campaign guidelines and their impact on compliance and mortality reduction

Read the detailed description

The implementation of the sepsis resuscitation bundle recommended by the SSC guidelines has been shown to increase compliance and reduce mortality in several settings. Different implementation strategies have been utilized, including education, posters, reminders, audit and feedback, paper-based and electronic sepsis screening tools, clinical pathway and sepsis response teams. Different studies showed a considerable variation effect on compliance and mortality.It has been suggested that implantation strategies vary in there effect from low impact for human-based interventions such as education and training, rules and policies, reminders, checklists and double checks, however, reaching high effect for system based interventions like automation and computerization and forcing function. However, this has not been studied in relation to the implementation of SSC bundle. As such, many projects continue to invest on low-impact interventions with modest change in compliance and mortality. Multiple interventions were adopted by different centers worldwide to implement SSC guidelines. These interventions vary on their level of compliance and outcomes. The effectiveness of intervention if system oriented is more effective than human oriented. The hierarchy of effectiveness assigning forcing function intervention on the top of the pyramid and the training and education on the bottom.

The investigators hypothesize that interventions system based interventions are more likely to be more effective in improving the compliance with sepsis resuscitation bundle and in improving mortality.

The aim of this study is to assess the effectiveness of different interventions for implementation of Surviving Sepsis Campaign guidelines and their impact on compliance and mortality reduction.

02

Conditions studied

  • Sepsis
  • Septic
  • Septicemia

Keywords

  • surviving sepsis campaign
  • sepsis
  • septic
  • septicemia
  • mortality
  • compliance
03

In context

Sepsis

1,946 studies on the registry are indexed under Sepsis; 471 are open to participants now.

This study's planned enrollment of 30 is below the median of 160 across 957 observational studies indexed under Sepsis.

Browse Sepsis studies →

Lead sponsor

King Abdullah International Medical Research Center is the lead sponsor of 46 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Research articles

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Any study or data

  1. assessing any intervention method for implementing SSC guidelines in regards to compliance and mortality,
  2. has a comparison group,
  3. reported data on sepsis resuscitation bundle compliance and mortality

Exclusion criteria

Exclusion Criteria:

Any study used other than SSC guidelines in sepsis management will be excluded.

05

Study design

Enrollment
30 participants (estimated)
Patient registry
No

Groups and cohorts

  • Low intensity intervention

    human oriented interventions with less consideration to the system based act including, but not limited to, education, training, sepsis profile and posters with protocol algorithms.

  • Intermediate intensity intervention

    interventions that lie in between human oriented and system oriented Including, but not limited to, sepsis protocols, daily audits, feedback and clinical pathway

  • High intensity intervention

    system based interventions with less involvement of human effect including, but not limited to, electronic alert systems and sepsis response team.

06

What researchers measure

Primary outcomes

  1. Surviving Sepsis Campaign (SSC) Guidelines Compliance and Mortality

    Time frame: 2002 - 2014 (12 years)

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 21, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02069028
Lead sponsor
King Abdullah International Medical Research Center
Responsible party
Dr Yaseen Arabi (Chairman, Intensive Care Department, Associate Professor, King Saud Bin Abdulaziz University, King Abdullah International Medical Research Center) — Principal investigator
First posted
Feb 21, 2014
Start date
Feb 2014
Primary completion
Jun 2014 (estimated)
Completion
Sep 2014 (estimated)
Last update
Feb 21, 2014

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Feb 2014. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion