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Clinical Trials/NCT01723137
NCT01723137
Completed
Not Applicable

Measuring Changes in Acute Pain in the Emergency Department Using Patient Reported Scales

Hennepin Healthcare Research Institute1 site in 1 country3,630 target enrollmentMay 2010
ConditionsAcute Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Pain
Sponsor
Hennepin Healthcare Research Institute
Enrollment
3630
Locations
1
Primary Endpoint
Change in Patient Described Stress
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

Patient reported pain, stress, and anxiety measures have been found to be inter-related, but it is not known if they are all associated with receiving opiate medications. The objective of this study is to determine if patients' degree of reported pain, stress, or anxiety is associated with receiving opiate pain medications in the emergency department or at discharge. Alert patients at least 18 years of age and who report pain greater than 3/10 are eligible to participate in the study. Consenting patients complete Visual Analog Scales describing their perceived pain, stress, and anxiety from enrollment until discharge. Demographic data and administration of pain medication is also recorded. Visual Analog Scale scores among patients who received an opioid pain medicine in the emergency department and at discharge will be compared to those who did not.

Registry
clinicaltrials.gov
Start Date
May 2010
End Date
January 2013
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Reported pain greater than or equal to 3 out of 10

Exclusion Criteria

  • Less than 18 years of age
  • Decreased level of consciousness
  • Inability to answer questions

Outcomes

Primary Outcomes

Change in Patient Described Stress

Time Frame: Immediately upon enrollment, every 30 minutes after until hospital discharge, and upon discharge, for up to 24 hours.

Patients describe stress by completion of 100 mm Visual Analog Scale, bordered by the words "no stress" and "most stress possible".

Change in Patient described anxiety.

Time Frame: Immediately upon study enrollment, every 30 minutes post-enrollment, and upon hospital discharge, for up to 24 hours.

Patients describe anxiety by completing 100mm Visual Analog Scale, bordered by the words "no anxiety" and "most anxiety possible".

Change in patient described satisfaction with ongoing treatment.

Time Frame: Immeditately upon enrollment, every 30 minutes post-enrollment, and upon hospital discharge, up to 24 hours.

Patients describe satisfaction with ongoing treatment by completion of 100mm Visual Analog Scale, bordered by the words "not satisfied at all" and "completely satisfied".

Change in patient described pain.

Time Frame: Immediately upon enrollment, every 30 minutes post-enrollment, and upon discharge, for up to 24 hours.

Patients describe pain by completing a 100mm Visual Analog Scale, bordered by the words "no pain" and "worst pain possible".

Study Sites (1)

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