- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02468869
Improving Discharge Communication in the Emergency Department Through Information Structuring
October 22, 2018 updated by: University Hospital, Basel, Switzerland
Improving Discharge Communication in the Emergency Department Through Information Structuring: A Cluster Randomized Controlled Trial
The goal of the proposed study is to assess the potential of information structuring for improving discharge communication.
Specifically, the investigators aim to examine the advantages of an information-structuring skills training for physicians (compared to an empathy skills training) on discharge communication and associated patient outcomes, such as patients' information recall and adherence to physician recommendations.
The investigators hypothesize that patients receiving structured discharge information from their trained physicians will be able to recall more information and show higher adherence to recommendations relative to controls (i.e., patients receiving discharge information from doctors trained in empathy skills).
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
196
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Baselstadt
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Basel, Baselstadt, Switzerland, 4031
- University Hospital Basel, Emergency Department
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Outpatients with chest pain
- Outpatients with abdominal pain
Exclusion criteria:
- Patients younger than 18 years of age (limited ability to provide informed consent)
- Patients with limited ability to communicate in German, the default language at the hospital (confounder related to language proficiency)
- Patients with dementia (confounder arising from pathological memory deficits)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Information structuring skills training
Physicians received a communication skills training focusing on information structuring with the so-called book metaphor for a structured discharge communication with the patient.
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Active Comparator: Empathy skills training
Physicians received a communication skills training focusing on empathy skills with the acronym NURSE for an empathetic discharge communication with the patient.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Patients' recall of the information provided during discharge communication
Time Frame: 3 times: immediately after discharge, one week after discharge, one month after discharge
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3 times: immediately after discharge, one week after discharge, one month after discharge
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Adherence to recommendations
Time Frame: 2 times: one week and one month after discharge
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2 times: one week and one month after discharge
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Patient satisfaction in four dimensions
Time Frame: Immediately after discharge
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(1) comprehension, (2) structuredness (3) recommendation of the physician to family and friends (4) informativeness
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Immediately after discharge
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Roland Bingisser, Prof. Dr., University Hospital, Basel, Switzerland
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 1, 2015
Primary Completion (Actual)
April 1, 2017
Study Completion (Actual)
April 1, 2017
Study Registration Dates
First Submitted
May 27, 2015
First Submitted That Met QC Criteria
June 8, 2015
First Posted (Estimate)
June 11, 2015
Study Record Updates
Last Update Posted (Actual)
October 23, 2018
Last Update Submitted That Met QC Criteria
October 22, 2018
Last Verified
October 1, 2018
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- BACOP2
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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