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Evaluation of Training in De-escalation

Primary Purpose

De-escalation Skills

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Training in de-escalation
Sponsored by
Bergen University College
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for De-escalation Skills focused on measuring De-escalation, Aggression, Violence prevention

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Third year nursing student

Exclusion Criteria:

  • Has to talk and understand Norwegian

Sites / Locations

  • Bergen University College

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Third year nursing students - intervention

Third year nursing students - control

Arm Description

Third year nursing students will receive the intervention in de-escalation training

Third year nursing students will receive no training in de-escalation

Outcomes

Primary Outcome Measures

Changes in de-escalation skills: Baseline
Instrument: "English Modified De-escalating Aggressive Behaviour Scale" (Mavandadi & Bieling, 2016)
Changes in de-escalation skills
Instrument: "English Modified De-escalating Aggressive Behaviour Scale" (Mavandadi & Bieling, 2016)
Changes in de-escalation skills
Instrument: "English Modified De-escalating Aggressive Behaviour Scale" (Mavandadi & Bieling, 2016)

Secondary Outcome Measures

Changes in coping and confidence
Instrument: "Clinicians confidence in coping with patient aggression" (Thackreys, 1987)
Changes in coping and confidence
Instrument: "Clinicians confidence in coping with patient aggression" (Thackreys, 1987)
Changes in coping and confidence
Instrument: "Clinicians confidence in coping with patient aggression" (Thackreys, 1987)

Full Information

First Posted
April 10, 2019
Last Updated
August 3, 2020
Sponsor
Bergen University College
Collaborators
Helse-Bergen HF
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1. Study Identification

Unique Protocol Identification Number
NCT03924141
Brief Title
Evaluation of Training in De-escalation
Official Title
Effects of a Brief De-escalation Training Program on Student Nurses' Skills and Confidence Level in Coping With Patient Aggression: a Cluster Randomized Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
February 18, 2019 (Actual)
Primary Completion Date
November 26, 2019 (Actual)
Study Completion Date
June 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bergen University College
Collaborators
Helse-Bergen HF

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to evaluate one of the chapters in the new national Norwegian training manual (MAP). The chapter that is selected to be evaluated is the chapter on de-escalation. Effective training in this topic should not only lead to changes in the level of knowledge and attitudes, but also changes in behavior and skills. Experiencing better preparedness does not necessarily entail a change in behavior. This study wants to test whether training in de-escalation changes the participants' skills and experience of self-confidence, security and coping in threatening situations.
Detailed Description
The theme is: • 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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
De-escalation Skills
Keywords
De-escalation, Aggression, Violence prevention

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
The outcomes assessors who will assess the video data will be blinded
Allocation
Randomized
Enrollment
45 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Third year nursing students - intervention
Arm Type
Experimental
Arm Description
Third year nursing students will receive the intervention in de-escalation training
Arm Title
Third year nursing students - control
Arm Type
No Intervention
Arm Description
Third year nursing students will receive no training in de-escalation
Intervention Type
Behavioral
Intervention Name(s)
Training in de-escalation
Intervention Description
Will receive one hour of de-escalation training
Primary Outcome Measure Information:
Title
Changes in de-escalation skills: Baseline
Description
Instrument: "English Modified De-escalating Aggressive Behaviour Scale" (Mavandadi & Bieling, 2016)
Time Frame
Immediately before and immediately after intervention (single day, baseline)
Title
Changes in de-escalation skills
Description
Instrument: "English Modified De-escalating Aggressive Behaviour Scale" (Mavandadi & Bieling, 2016)
Time Frame
Immediately before and immediately after intervention (single day, 6 months post-baseline)
Title
Changes in de-escalation skills
Description
Instrument: "English Modified De-escalating Aggressive Behaviour Scale" (Mavandadi & Bieling, 2016)
Time Frame
Immediately before and immediately after intervention (single day, 9 months post-baseline)
Secondary Outcome Measure Information:
Title
Changes in coping and confidence
Description
Instrument: "Clinicians confidence in coping with patient aggression" (Thackreys, 1987)
Time Frame
Immediately before and immediately after intervention (single day, baseline)
Title
Changes in coping and confidence
Description
Instrument: "Clinicians confidence in coping with patient aggression" (Thackreys, 1987)
Time Frame
Immediately before and immediately after intervention (single day, 6 months post-baseline)
Title
Changes in coping and confidence
Description
Instrument: "Clinicians confidence in coping with patient aggression" (Thackreys, 1987)
Time Frame
Immediately before and immediately after intervention (single day, 9 months post-baseline)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Third year nursing student Exclusion Criteria: Has to talk and understand Norwegian
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kjersti Alsaker, PhD
Organizational Affiliation
Bergen University College
Official's Role
Study Chair
Facility Information:
Facility Name
Bergen University College
City
Bergen
Country
Norway

12. IPD Sharing Statement

Plan to Share IPD
No

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Evaluation of Training in De-escalation

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