NCT02927054

Brief Summary

A questionnaire was provided, including clinical vignettes and free text answers, to assess and evaluate the ability of resident physicians to identify systemic inflammatory response syndrome (SIRS), sepsis, and severe sepsis. Questionnaire scores were compared between specialties. A whole-hospital educational campaign was provided with the aim to improve sepsis recognition, and the questionnaire survey was repeated after one year to assess the effect of the education on the recognition of sepsis.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
239

participants targeted

Target at P50-P75 for not_applicable sepsis

Timeline
Completed

Started Jul 2014

Typical duration for not_applicable sepsis

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2014

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2016

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

October 5, 2016

Completed
1 day until next milestone

First Posted

Study publicly available on registry

October 6, 2016

Completed
Last Updated

October 6, 2016

Status Verified

October 1, 2016

Enrollment Period

2.2 years

First QC Date

October 5, 2016

Last Update Submit

October 5, 2016

Conditions

Outcome Measures

Primary Outcomes (1)

  • Change in sepsis recognition and treatment survey score

    Questionnaire scores assessing sepsis recognition and treatment at baseline compared to a similar survey following one year of whole-hospital educational campaign, across groups of residents of different training backgrounds

    Baseline and 1 Year

Study Arms (5)

Internal Medicine Residents

OTHER

Sepsis education provided to internal medicine residents

Other: Sepsis Education

Emergency Medicine Residents

OTHER

Sepsis education provided to emergency medicine residents

Other: Sepsis Education

Orthopedic Residents

OTHER

Sepsis education provided to orthopedic residents

Other: Sepsis Education

Neurosurgery Residents

OTHER

Sepsis education provided to neurosurgery residents

Other: Sepsis Education

General Surgery Residents

OTHER

Sepsis education provided to general surgery residents

Other: Sepsis Education

Interventions

Education provided to hospital residents for the recognition and treatment of systemic inflammatory response syndrome (SIRS), sepsis and severe sepsis

Emergency Medicine ResidentsGeneral Surgery ResidentsInternal Medicine ResidentsNeurosurgery ResidentsOrthopedic Residents

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Resident physician in an University of Utah training program

You may not qualify if:

  • Not willing to participate

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (2)

  • Poeze M, Ramsay G, Gerlach H, Rubulotta F, Levy M. An international sepsis survey: a study of doctors' knowledge and perception about sepsis. Crit Care. 2004 Dec;8(6):R409-13. doi: 10.1186/cc2959. Epub 2004 Oct 14.

    PMID: 15566585BACKGROUND
  • Assuncao M, Akamine N, Cardoso GS, Mello PV, Teles JM, Nunes AL, Maia MO, Rea-Neto A, Machado FR; SEPSES Study Group. Survey on physicians' knowledge of sepsis: do they recognize it promptly? J Crit Care. 2010 Dec;25(4):545-52. doi: 10.1016/j.jcrc.2010.03.012. Epub 2010 Jun 19.

MeSH Terms

Conditions

SepsisSystemic Inflammatory Response Syndrome

Condition Hierarchy (Ancestors)

InfectionsInflammationPathologic ProcessesPathological Conditions, Signs and SymptomsShock

Study Officials

  • Devin J Horton, MD

    University of Utah

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 5, 2016

First Posted

October 6, 2016

Study Start

July 1, 2014

Primary Completion

September 1, 2016

Study Completion

September 1, 2016

Last Updated

October 6, 2016

Record last verified: 2016-10

Data Sharing

IPD Sharing
Will share

If requested, will share with other authors or institutions