- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02359071
Shift Characteristics Affect Handover Duration and Rates. (Handover)
November 19, 2015 updated by: Atıf, Ataturk University
Which Shift Characteristics Affect Handover Duration and Rates? A Prospective Multicentric Study
The primary aim of our study was to analyze the independent factors affecting handover duration in Emergency Department.
The secondary aim was to identify the factors affecting Emergency Department handover rates.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The primary aim in this study was to analyze the independent factors affecting handover duration in Emergency Department.
Our secondary aim was to identify the factors affecting the Emergency Department handover rates.
To better analyze independent variables, we dichotomized the data.
First, we dichotomized handover duration into two groups according to the median handoff time of 20 minutes.
Second, we divided handover rates into two groups using the median rate of handovers per shift, which was 3.87%.
Study Type
Observational
Enrollment (Actual)
267
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
16 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
we obtained data streams from seven centers, and 267 completed records from different centre were included.
Description
Inclusion Criteria:
The day and night shift handover , which are the interactive, verbal, bedside, and face-to-face interactions between the outgoing and incoming medical staff, were included.
Exclusion Criteria:
Handover locations other than bedside (n=3), handover methods except verbal communication (by paper (n=2)), and the use of information technology (n=1) were excluded to standardize the procedure.
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
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Handovers with lower durations
equal or lower than 20 minutes
|
To better analyze independent variables, we dichotomized the data.
First, we dichotomized handover duration into two groups according to the median handoff time of 20 minutes.
Second, we divided handover rates into two groups using the median rate of handovers per shift, which was 3.87%.
|
|
handovers with higher durations
Higher than 20 minutes
|
To better analyze independent variables, we dichotomized the data.
First, we dichotomized handover duration into two groups according to the median handoff time of 20 minutes.
Second, we divided handover rates into two groups using the median rate of handovers per shift, which was 3.87%.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
the independent factors affecting handover duration in Emergency Department
Time Frame: 1-30 September 2013
|
1-30 September 2013
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
to identify the factors affecting Emergency Department handover rates.
Time Frame: 1-30 September 2013
|
1-30 September 2013
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Ali Karakus, Assoc. prof, Mustafa Kemal University
- Principal Investigator: Ayhan Sarıtas, Assoc. prof, Duzce University
- Principal Investigator: Gulhan Kurtoglu, specialist, Ankara Training and Research Hospital
- Principal Investigator: Ozlem Bilir, Assist. Prof, Recep Tayyip Erdoğan University
- Principal Investigator: Ayhan Akoz, Assoc. prof., Ataturk University
- Principal Investigator: Murat Eroglu, Assoc. prof, GATA Haydarpasa Military Hospital
- Principal Investigator: Onur Karakayali, specialist, DerinceTraining and Research Hospital
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
September 1, 2013
Primary Completion (Actual)
October 1, 2013
Study Completion (Actual)
October 1, 2013
Study Registration Dates
First Submitted
February 4, 2015
First Submitted That Met QC Criteria
February 6, 2015
First Posted (Estimate)
February 9, 2015
Study Record Updates
Last Update Posted (Estimate)
November 20, 2015
Last Update Submitted That Met QC Criteria
November 19, 2015
Last Verified
February 1, 2015
More Information
Terms related to this study
Other Study ID Numbers
- Atıf-001
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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