NCT00470652

Brief Summary

Oligoanalgesia1 has been widely recognized as an issue in emergency department.The purpose of our study is to assess the impact of the implementation of a computer-assisted support program to improve pain management in our ED.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
631

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2007

Geographic Reach
1 country

1 active site

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

May 1, 2007

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

May 4, 2007

Completed
4 days until next milestone

First Posted

Study publicly available on registry

May 8, 2007

Completed
1.3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2008

Completed
Last Updated

January 27, 2009

Status Verified

January 1, 2009

First QC Date

May 4, 2007

Last Update Submit

January 26, 2009

Conditions

Keywords

painPain MeasurementDecision Making, Computer-AssistedInformatics

Study Arms (3)

1

Pre-intervention patients admitted to our ED in the month prior to the intervention, before the 'computer-assisted decision support' is turned on (the intervention)

2

Short-term post-intervention cohort of patients admitted in the month following the initiation of the 'computer-assisted decision support' for pain management

Device: computer-assisted decision support

3

long-term post-intervention cohort of patients admitted on the 6th month following the initiation of the 'computer-assisted decision support' for pain management

Device: computer-assisted decision support

Interventions

at the end of the pre-intervention period, the patient flow software was modified to open popup windows automatically when pain intensity was not documented or pain was not reevaluated within the recommended interval. The popup window also detailed appropriate pain treatment guidelines based on the documented pain intensity. In addition, the patient's icon in the flow software changed from black to red when pain intensity was \>4/10. After a 10-day test period, the post-intervention data collection started.

Also known as: informatics, information technology
23

Eligibility Criteria

Age16 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Consecutive patients discharged from our ED who either had pain on admission or suffered of a new pain while in our ED

You may qualify if:

  • Any patient admitted to our Emergency Department who is
  • age \> 16 years
  • pain lasting =\< 1 week or
  • no pain on admission but pain during the ED stay

You may not qualify if:

  • life-threatening condition requiring immediate admission in the OR or ICU
  • no pain or pain lasting \>1 week
  • inability to give informed consent (intoxicated, psychiatric disorder, language problem, prisoner)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre Hospitalier Universitaire Vaudois

Lausanne, Canton of Vaud, 1011, Switzerland

Location

Related Publications (1)

  • Decosterd I, Hugli O, Tamches E, Blanc C, Mouhsine E, Givel JC, Yersin B, Buclin T. Oligoanalgesia in the emergency department: short-term beneficial effects of an education program on acute pain. Ann Emerg Med. 2007 Oct;50(4):462-71. doi: 10.1016/j.annemergmed.2007.01.019. Epub 2007 Apr 18.

    PMID: 17445949BACKGROUND

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Olivier W Hugli, MD,MPH

    Centre Hospitalier Universiataire Vaudois

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

May 4, 2007

First Posted

May 8, 2007

Study Start

May 1, 2007

Study Completion

September 1, 2008

Last Updated

January 27, 2009

Record last verified: 2009-01

Locations