Posturing Effects on Perception of Time and Perceptions of the Provider-Patient Interaction in the Emergency Department

NCT00170105 | Completed DMC

• 1 other identifier: 1487-05
• Study Type: observational
• Target: 244
• Locations: 1 country
• Sites: 1

Brief Summary

Study Objective:

• To examine the perceptions of time spent at the bedside; perceptions of bedside manner; and patient perceptions of the provider-patient interaction offered by emergency providers when they sit versus when they stand during the initial evaluation. This project is clinically relevant research different from prior Emergency Department (ED) satisfaction studies since this study will contribute information about factors that could increase patient satisfaction with his/her provider in the ED setting. This research may guide specific guidelines for quality improvement efforts. The investigators hypothesize that patients will perceive that the emergency providers are at the bedside longer, demonstrate better bedside manner, and have better provider-patient interactions when they sit versus when they stand. Additionally, the investigators hypothesize that providers who sit will perceive that they are at the bedside longer than those who stand for the same period of time. Methods: A convenience sample of adult patients will complete a 5-item questionnaire concerning the perceived time spent with the emergency provider and the qualities of the provider-patient interaction. Emergency providers will be randomly assigned to either sit or stand during the initial evaluation. The providers will complete a 4-item questionnaire. These data will be compared to the actual time spent in the evaluation, measured in seconds, using a stopwatch. These data, combined with demographic data obtained from the patient chart, will be analyzed to examine whether there are statistically significant differences in patient perceptions and satisfaction.

Conditions

Healthy

Keywords

Age 18 years or older; No cognitive impairment or altered mental status; Stable; No aphasia; English-speaking

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

•- The subject population represents a convenience sample of patients 18 years and older who give consent. * All English speaking individuals with adequate health status and cognitive function to communicate answers to the investigator. * There are no foreseen reasons to exclude pregnant women as they are not likely to be vulnerable in this study.

You may qualify if:

• The subject population represents a convenience sample of patients 18 years and older who give consent.
• All English speaking individuals with adequate health status and cognitive function to communicate answers to the investigator.
• There are no foreseen reasons to exclude pregnant women as they are not likely to be vulnerable in this study.

You may not qualify if:

• Unstable patients and patients seen in the critical care area will be excluded from study.

Sponsors & Collaborators

• Mayo Clinic: lead

Study Sites (1)

Mayo Clinic

Rochester, Minnesota, 55905, United States

Location

Study Officials

• Annie T. Sadosty, M.D.

  Mayo Clinic

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER

Study Record Dates

• First Submitted: September 13, 2005
• First Posted: September 15, 2005
• Study Start: August 1, 2005
• Primary Completion: August 1, 2006
• Study Completion: August 1, 2006
• Last Updated: February 2, 2010

Record last verified: 2010-02

Locations

US (1)