Posturing Effects on Perception of Time and Perceptions of the Provider-Patient Interaction in the Emergency Department
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Purpose
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.
| Study Type: | Observational |
| Study Design: | Time Perspective: Prospective |
| Official Title: | Posturing Effects on Perception of Time and Perceptions of the Provider-Patient Interaction in the Emergency Department |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
•- 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.
Inclusion Criteria:
- 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.
Exclusion Criteria:
- Unstable patients and patients seen in the critical care area will be excluded from study.
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Annie T. Sadosty, M.D., Mayo Clinic |
| ClinicalTrials.gov Identifier: | NCT00170105 History of Changes |
| Other Study ID Numbers: | 1487-05 |
| Study First Received: | September 13, 2005 |
| Last Updated: | February 1, 2010 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Mayo Clinic:
|
Age 18 years or older No cognitive impairment or altered mental status Stable No aphasia English-speaking |
Additional relevant MeSH terms:
|
Emergencies Disease Attributes Pathologic Processes |
ClinicalTrials.gov processed this record on May 23, 2013