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

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.

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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