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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05946720
Other study ID # 117
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2021
Est. completion date April 14, 2022

Study information

Verified date July 2023
Source Mugla Sitki Koçman University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The research, was planned in a randomized controlled design, aiming to evaluate the effect of the training given to nurses working in psychiatric clinics on the use of aggression and BVC (Broset Violence Checklist) on the nurses' perceptions of aggression and the compliance of the use of BVC, which they evaluated for the patients watched in the videos, with the BVC determined by expert opinion. The study was conducted in Adana Doctor Ekrem Tok Mental Health and Diseases Hospital between July 2021 and April 2022. A total of 97 nurses working in psychiatric clinics, 47 in the training group and 50 in the comparison group, participated in the study. A pre-test was administered to the nurses and nurses in the training group were randomized and given training including aggression and BVC use. After the training, a post-test was administered to all nurses.


Recruitment information / eligibility

Status Completed
Enrollment 97
Est. completion date April 14, 2022
Est. primary completion date July 10, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Volunteering to participate in the research, - To have been working in the hospital where the research was conducted for at least 1 year, - To have no vision, hearing and speech problems. Exclusion Criteria: - To want to withdraw from the research at any stage of the research, - Not completing or not being able to complete the research for any reason, - To work in the filiation team during the research process.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Training including aggression and the use of BVC.
After obtaining verbal consent from the nurses who met the inclusion criteria of the study before the pre-test was applied to the nurses, the nurses who volunteered to participate in the study were randomized within their own clinic using the simple randomization method. For this, after the data collection form was distributed before the pre-test, the nurses were asked to write the letter that came to them on the data collection form and not forget it. In order for nurses to be included in the training or comparison group, the letter A, written on the closed papers in the box prepared for simple randomization, represents the Education group, and the letter B represents the comparison group.

Locations

Country Name City State
Turkey Çukurova Üniversitesi Adana

Sponsors (1)

Lead Sponsor Collaborator
Mugla Sitki Koçman University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Perception of Aggression Scale The scale has a 5-point Likert-type rating system ranging from strongly disagree (1) to strongly agree (5) and consists of 29 items. The items have two subscales: functional (functional - acceptable / healthy response) and dysfunctional (dysfunctional - unacceptable / undesirable aggression). For each subscale, the average of the relevant item scores will be calculated. Procedure (one week before the training)
Primary Broset Violence Checklist A score of "1" is given in the presence of each item of the BVC, and "0" in the absence of it. In the next evaluations of the patient, if there is an increase in the relevant item compared to the previous one, the behavior score is scored as "1", the habitual or same level behavior is considered absent and scored as "0". If there is no more in the case of a patient with a flood than before, the relevant item score should be "0". If an increase in the level of exuberance is observed, it should be scored as "1". After the six items are scored in this way, the evaluation is made over the total score. A total score of "0" indicates that the patient has a low severity risk level. "1- 2 points" indicates moderate risk of violence and necessitates measures to prevent violence. "3-6 points" refers to a high risk of violence. Procedure (one week before the training and one day after the training)
Primary Perception of Aggression Scale The scale has a 5-point Likert-type rating system ranging from strongly disagree (1) to strongly agree (5) and consists of 29 items. The items have two subscales: functional (functional - acceptable / healthy response) and dysfunctional (dysfunctional - unacceptable / undesirable aggression). For each subscale, the average of the relevant item scores will be calculated. Procedure (one day after the training)
Primary Broset Violence Checklist A score of "1" is given in the presence of each item of the BVC, and "0" in the absence of it. In the next evaluations of the patient, if there is an increase in the relevant item compared to the previous one, the behavior score is scored as "1", the habitual or same level behavior is considered absent and scored as "0". If there is no more in the case of a patient with a flood than before, the relevant item score should be "0". If an increase in the level of exuberance is observed, it should be scored as "1". After the six items are scored in this way, the evaluation is made over the total score. A total score of "0" indicates that the patient has a low severity risk level. "1- 2 points" indicates moderate risk of violence and necessitates measures to prevent violence. "3-6 points" refers to a high risk of violence. Procedure (one day after the training)
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