Efficacy of Bystander Intervention Program in Nursing Students

July 30, 2025 updated by: Seda Er, Istanbul University - Cerrahpasa

The Effect of Bystander Intervention Program on Bystander Efficacy, Behavior and Intent to Help for Dating Violence in Nursing Students

The research will be conducted in a randomized control group experimental research design. The study aims to evaluate the effectiveness of the bystander intervention program developed for dating violence in nursing students. The Bystander Intervention Program will be developed after a literature review on the subject and taking into account previous evidence-based research. The population of the study will consist of Istanbul University-Cerrahpaşa Florence Nightingale Faculty of Nursing, Department of Nursing, Turkish Program 1st year students (N=130). In the sample size calculation, the data reported in similar studies in the literature were used (Rothman et al. 2018). The representativeness of the study was calculated as β=80%, α=0.05 (effect size: 0.6), and a total of 80 samples were calculated as a result of power analysis, 40 intervention, and 40 control groups. Participants will be assigned to the experimental or control group by computer-based simple randomization method. Data will be collected between September, 19 2024, and December 19, 2024. Data will be collected face-to-face using the Individual Information Form, Bystander Efficacy Scale, Intention to Help Scale-Short Version, Bystander Behavior Scale (For Friends), and Program Evaluation Form. The data obtained from the research will be evaluated with the SPSS package program.

Study Overview

Detailed Description

Dating violence is defined as the tendency to force a person, to establish power and control over a person. Dating violence is a public health problem for all countries in the world (WHO, 2021; Kerman & Öztürk, 2022). According to the results of studies conducted with university students; more than 70% of students are exposed to dating violence (Schuster et al., 2016; Toplu-Demirtaş & Fincham, 2020). In addition, it is stated in studies that dating violence starts before the age of 25 (Peterson et al., 2018; Park & Kim, 2021). Young people exposed to violence may have difficulty seeking help, hide the violence, and feel obliged to maintain the relationship (Park & Kim, 2021). Studies have shown that college students exposed to dating violence experience many negative physical and mental problems, including physical injuries, depression, anxiety, decreased academic performance, and drug and alcohol abuse (Choi et al., 2017).

One of the ways to reduce the risk of dating violence is to focus on other bystanders. It is seen that programs developed to prevent violence are shaped around bystander intervention (Banyard et al., 2019). Bystander intervention, an evidence-based intervention to prevent dating violence, is defined as "an initiative that focuses on adolescents or young adults who have the necessary skills and self-efficacy to safely intervene when they witness dating violence and sexual violence" (Storer, 2016). Bystanders can contribute to risk reduction directly (e.g. by calling security, intervening directly) or indirectly (e.g. by challenging negative attitudes towards dating violence) when dating violence occurs (Amar et al., 2015; Banyard et al., 2019; Debnam and Mauer, 2019; Finnie et al., 2022). Recent studies have found that bystander intervention programs applied to young people produce statistically significant results in the areas of (1) knowledge about dating violence (prevalence, definitions, etc.); (2) attitudes towards dating violence (decrease in sexist attitudes, decrease in denial of violence as a problem, increase in confidence to intervene, increase in intention to intervene, increase in students' self-efficacy to take action against violence, etc.) and (3) behavioral change (decrease in violence perpetration rate, etc.) (Amar et al. 2015; Jouriles et al. 2018; Peterson et al. 2018). ) and (3) behavior change (decreased rate of violence perpetration, etc.) (Amar et al. 2015; Jouriles et al. 2018; Peterson et al. 2018).

Nurses are one of the first intervention health professionals in the care of individuals exposed to violence. Providing direct care to the individual subjected to violence and advocating for resources focused on preventing violence is one of the responsibilities and roles of nursing care. It is stated that mental health nurses can apply bystander education principles in prevention programs that aim to change community norms regarding violence (Amar et al. 2012; Kerman & Öztürk, 2022). It is stated that it is important for nursing students, who will be among the health professionals of the future, to develop knowledge, skills, and attitudes about what to do when they witness violence (Barroso-Corroto ve ark., 2022). There are different bystander intervention programs used to prevent dating violence in the literature (Debnam & Mauer, 2019). However, there is no bystander intervention program developed for dating violence for university students in Turkey. Accordingly, this study aims to evaluate the effectiveness of the bystander intervention program developed for dating violence in nursing students.

Study Type

Interventional

Enrollment (Actual)

83

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Şişli/Istanbul
      • Istanbul, Şişli/Istanbul, Turkey, 34381
        • Istanbul University-Cerrahpasa

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Between the ages of 18-24
  • Active student enrollment in the nursing department of the faculty in the academic year 2023-2024
  • Filled in forms and scales

Exclusion Criteria:

  • No active student enrollment in the nursing department of the faculty in the academic year 2023-2024 (due to reasons such as freezing enrollment, transferring to another institution, etc.)
  • Participation in seminars/workshops/group work/conferences/congresses/seminars/trainings etc. on prevention of dating violence and/or bystander intervention

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

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental Group
Participants in this group will have the Bystander Intervention Program for Dating Violence. The aim of this program, which will be prepared taking into account the needs of the country and institutions, is to provide knowledge and skills to safely intervene in dating violence. The program will be implemented at a convenient time for the experimental group of students within the 2023-2024 Spring semester academic calendar, taking into account the 1st-grade course schedule of Istanbul University-Cerrahpaşa Florence Nightingale Faculty of Nursing.

The Bystander Intervention Program for Dating Violence includes the following topics: Dating violence and its types (Session 1), risk factors and consequences of dating violence (Session 2), bystander intervention in dating violence and barriers to intervention (Session 3), bystander intervention strategies for dating violence (Session 4), self-care for bystanders witnessing dating violence (Session 5).

Each session is planned to last 60-90 minutes. Materials will be used in the Bystander Intervention Program for Dating Violence are PPT (PowerPoint Presentations) slides, videos, interactive scenarios, and group discussions. The Bystander Intervention Program for Dating Violence is planned to be applied face-to-face in 4 groups (12, 10, and 10 people) at scheduled times in a quiet room suitable for the group.

No Intervention: Control Group
The control group will not participate in the Bystander Intervention Program for Dating Violence, an interview consisting of one session is planned considering for the placebo effect. The control group students will be given a single 60-minute information session on dating violence and the students will be expected to fill out the scales to be filled out within the scope of the research at the pre-test and post-test times. At the end of the study, the Bystander Intervention Program for Dating Violence will be carried out with the voluntary participants in the control group, taking into account the ethics.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Bystander Efficacy Scale
Time Frame: It will be applied to both groups within one week before the program, and within 1 week after the program is completed
The scale used to assess bystander effectiveness was developed by Banyard et al. The scale includes 18 items. The participant is expected to indicate his/her degree of confidence by writing a whole number between 0-100 to indicate how confident he/she is that he/she can perform the behaviors specified in the scale. The calculation is made by averaging all items and the scale has no cut-off point. High scores indicate a high degree of confidence. In the study conducted by Banyard et al. (2014), the Cronbach's alpha value of the scale was .93 and the mean was 72.60.
It will be applied to both groups within one week before the program, and within 1 week after the program is completed
Intention to Help Scale-Short Version
Time Frame: It will be applied to both groups within one week before the program, and within 1 week after the program is completed
The scale, which assesses the likelihood or willingness of participants to engage in various helping behaviors, was developed by Banyard et al. (2014). There are two separate subscales by creating separate but parallel items and it consists of 18 items in total. Participants are expected to rate their likelihood of performing the behaviors using a 5-point Likert-type scale. The scale is calculated by averaging the answers given to the items. High scores indicate that the individual is more likely to engage in helping behavior. Cronbach's alpha value for the short version of the scale was .93 (Banyard et al. 2014).
It will be applied to both groups within one week before the program, and within 1 week after the program is completed
Bystander Behavior Scale (For Friends)
Time Frame: It will be applied to both groups 2 months after the program
The scale used to determine the spectator behavior of the participants in the last 2 months was developed by Banyard et al. The scale has 44 items and includes only spectator behaviors towards friends. The scale consists of 4 factors. Participants are expected to mark "Yes", "No" and "Did not meet" for the fulfillment of each item. In the evaluation, each no sign is calculated as 0 points and each yes sign is calculated as 1 point. The items that individuals said they did not encounter are not included in the scoring and the calculation is made by taking the average of the answers given to the other items. Higher scores indicate the types of bystander behavior reported by more people. Cronbach's alpha value for the short version of the scale was .971 (Banyard et al. 2014).
It will be applied to both groups 2 months after the program

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Sevim Buzlu, PhD,RN, Istanbul University - Cerrahpasa

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 (Actual)

December 10, 2024

Primary Completion (Actual)

April 10, 2025

Study Completion (Actual)

June 13, 2025

Study Registration Dates

First Submitted

December 2, 2023

First Submitted That Met QC Criteria

December 11, 2023

First Posted (Actual)

December 20, 2023

Study Record Updates

Last Update Posted (Actual)

July 31, 2025

Last Update Submitted That Met QC Criteria

July 30, 2025

Last Verified

July 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • IU-Cerrahpaşa (IUC)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

There is not a plan to make IPD (Individual Participant Data) available. After the study is completed, the publication which includes the data results will be available.

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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