Skip to main content
Clinical Trials/NCT04717518
NCT04717518
Completed
Not Applicable

Anchoring Patients Pain Scores in the Emergency Department

CHRISTUS Health1 site in 1 country108 target enrollmentAugust 24, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Abdominal Pain
Sponsor
CHRISTUS Health
Enrollment
108
Locations
1
Primary Endpoint
Utilization of a questionnaire to measure the mean pain scores between two intervention groups based on the numeric pain score scale
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The proposed research will be a prospective, observational study to test the hypothesis that anchoring will affect verbal pain scores in the emergency department. There will be a small retrospective aspect to this study to obtain patient satisfaction ratings.

Detailed Description

The investigators will evaluate a convenience sample of patients presenting to the ED with a complaint of pain. Patients will be consented for participation and will fill out a brief survey concerning the current visit in the ED. There will be two forms of the survey. Participants will be randomly assigned to one of the two survey forms. Participants will first be asked if their pain score for this visit is greater than or less than an anchor number provided. In this survey, the investigators will use 20 and 80 as our anchoring numbers. The participants will then have a follow up question asking them to estimate their pain score on a 0-100 scale. Investigators will then perform a chart review to determine patient satisfaction scores for that specific visit to determine if the anchoring effect has any input on patient satisfaction scores.

Registry
clinicaltrials.gov
Start Date
August 24, 2020
End Date
November 12, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Landry Dorsett, DO

Principal Investigator

CHRISTUS Health

Eligibility Criteria

Inclusion Criteria

  • 18 years of age or older
  • Presenting to the ED with a chief complaint of any type of pain

Exclusion Criteria

  • Under 18 years of age
  • Refusal to consent
  • Incarcerated patients
  • Pregnant patients
  • Unable to complete survey secondary to clinical instability, severe pain, or disorientation determined by a study physician

Outcomes

Primary Outcomes

Utilization of a questionnaire to measure the mean pain scores between two intervention groups based on the numeric pain score scale

Time Frame: Through study completion, an average of 1 year

A questionnaire will be used to measure pain scores by utilizing a numeric pain scale (0-100) and measure the effect of anchoring bias on pain scores in the Emergency Department. It is hypothesized that a lower pain score anchor will lead to a lower reported pain score by the patient.

Secondary Outcomes

  • An analysis to examine the influence of anchoring on patient satisfaction for patients with common chief complaints related to pain in the Emergency Department. It is unknown if anchoring affects a patient's overall satisfaction.(Through study completion, an average of 1 year)

Study Sites (1)

Loading locations...

Similar Trials