Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
45 participants
INTERVENTIONAL
2019-02-18
2020-06-30
Brief Summary
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Detailed Description
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• Evaluation of the training program of de-escalation for third-year nursing students
Underlying research questions will be:
* Will the intervention provide increased de-escalation skills?
* Will training in de-escalation provide increased confidence in coping with patient aggression?
The design used to answer the research questions is a cluster-randomized controlled study with an intervention group and a control group.
The two study groups with nursing students will be exposed to two different scenarios (A and B) with simulated patient situations. Students will conduct simulation A before the intervention and simulation B the same day after the intervention. A control group will also be included which will review scenarios A and B without intervention. The purpose of this is to see if the scenarios in isolation give any effect on the pre- and post-measurements.
Participants will also be asked to complete a questionnaire (Thackreys, 1987) related to experienced coping security related to aggression management at four different times.
The scenarios will be recorded on video. Following all video data collection, 2 de-escalation experts will independently review the video data and quantify it using the EMDABS instrument. They will be blinded and not aware of whether the video was recorded before or after the intervention. The data that this generates will then be statistically examined.
The selection of participants will be made from three classes with third year nursing students. The classes consist of about 50 students. Participation is voluntary.
It is uncertain how many will participate, but on the basis of practical limits there is an upper limit of 15 participants per class for the intervention group (the selection is recruited from two classes), and 30 participants from the control group (the selection is recruited from a class). A total of n = 30 is desired in both the intervention group and the control group.
The following two outcomes will be analyzed; de-escalating behavior (EMDABS, Mavandadi et al., 2016) and confidence in coping with patient aggression (Thackrey, 1987).
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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Third year nursing students - intervention
Third year nursing students will receive the intervention in de-escalation training
Training in de-escalation
Will receive one hour of de-escalation training
Third year nursing students - control
Third year nursing students will receive no training in de-escalation
No interventions assigned to this group
Interventions
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Training in de-escalation
Will receive one hour of de-escalation training
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
60 Years
ALL
No
Sponsors
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Helse-Bergen HF
OTHER
Bergen University College
OTHER
Responsible Party
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Thomas Nag
Advisor
Principal Investigators
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Kjersti Alsaker, PhD
Role: STUDY_CHAIR
Bergen University College
Locations
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Bergen University College
Bergen, , Norway
Countries
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Other Identifiers
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716537
Identifier Type: -
Identifier Source: org_study_id
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