Impacts of the VEGA Family Violence Education Resources for Psychology Trainees

November 23, 2024 updated by: Elisa Romano, University of Ottawa

The Effects of the ©Violence, Evidence, Guidance, and Action (VEGA) Family Violence Education Resources on Canadian Clinical Psychology Students' Attitudes, Knowledge, and Behaviours

The current research project aims to assess the effectiveness of the ©Violence, Evidence, Guidance, and Action (VEGA) Family Violence Education Resources (VEGA Project, 2019) in improving the knowledge, self-efficacy, and clinical responses of clinical psychology doctoral students to family violence in clinical settings. The VEGA on-line training is a collection of family violence online education resources designed to inform health and social service practitioners about family violence in a Canadian context, including definitions of family violence, mandatory reporting duties, effective responding to survivors, and more. Participants in this trial will be doctoral students recruited from accredited Clinical Psychology programs across Canada. Participants will be assigned to an intervention or wait-list control group, and the outcome measures consist of knowledge and attitudes about family violence, as well as measures of skills relevant to appropriately responding to survivors in clinical settings. Further, participants will be invited to complete a qualitative interview after the intervention to discuss overall impressions of the training and other ways the training changed their perspectives, if at all, on family violence.

Study Overview

Status

Recruiting

Conditions

Detailed Description

The goal of the current research is to conduct a randomized controlled trial of the ©Violence, Evidence, Guidance, and Action (VEGA), Family Violence Education Resources (VEGA Project, 2019) among a sample of clinical psychology graduate students across Canadian universities to assess whether it is effective in improving responses to child maltreatment and intimate partner violence (IPV) (collectively referred too throughout as "family violence") in clinical settings. For this study, students belonging to accredited Clinical Psychology doctoral programs from Canadian universities will be randomized into either (a) an intervention group that will complete the online VEGA Family Violence Education Resources, OR (b) a control group who will not complete the training (but who will have the opportunity to do so following the completion of outcome data collection ; wait-list control). Throughout this evaluation study, a variety of pre- and post-training outcome measures will be administered participants; these measures are intended to assess reactions to the training, changes in family violence knowledge, changes in attitudes toward IPV and child maltreatment, and clinically relevant behaviours in responding to suspicions and disclosures of family violence by clients/patients in clinical practice settings. After completing the measures and the training, a subset of randomly selected students from the intervention group will be invited to participate in a one-on-one qualitative interview with a member of the research team via Zoom, during which they will be asked to share their perspectives on the training and how it impacted/may impact their work (or not) with clients who have experienced IPV and/or child maltreatment. Information provided from the quantitative measures and qualitative interviews will allow us to answer the following questions: (1) Was the training engaging and relevant to clinical psychology students? (2) Was the training able to improve the knowledge and self-efficacy of students regarding family violence? (3) Was the training able to change behaviours and improve the response of clinical psychology students to clients (or future clients) experiencing family violence in their professional training settings? Note: Used with permission from © 2020 VEGA Project, McMaster University. All rights reserved. All questions regarding the use and evaluation of the VEGA Family Violence Education Resources, or the VEGA Project more generally, should be directed to Dr. Melissa Kimber at vega@mcmaster.ca

Study Type

Interventional

Enrollment (Estimated)

90

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 Contact

  • Name: Carl Newton, M.A., Applied Psychology
  • Phone Number: 1-613-562-5800
  • Email: cnewt058@uottawa.ca

Study Contact Backup

  • Name: Elisa Romano, PhD, Clinical Psychology
  • Phone Number: 1-613-562-5800
  • Email: eromano@uottawa.ca

Study Locations

    • Ontario
      • Ottawa, Ontario, Canada, K1N 6N5
        • Recruiting
        • University of Ottawa - Child Wellbeing Lab
        • Contact:

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
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Be a student in the Clinical Psychology graduate program of a Canadian university.
  • Be engaged in clinical work as part of program requirements
  • Speak and read English
  • Have internet access

Exclusion Criteria:

-Currently participating in any other training relating to child maltreatment or intimate partner violence outside of mandatory or elective course material.

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: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: VEGA Family Violence Education Resources
Students in this arm will receive access to the online VEGA Family Violence Education Resources and will be asked to complete modules covering information about family violence in Canada, creating safety for survivors in clinical settings, recognizing and responding to child maltreatment and intimate partner violence, three interactive learning scenarios, and voices of those with lived experiences of family violence.

The VEGA Family Violence Education Resources (© 2020 VEGA Project, McMaster University) is an on-line suite of educational resources that target professionals who are likely to encounter survivors of family violence in professional and clinical settings. The resources provide information about family violence, appropriate clinical responses, legal obligations, and more. The resources are broken down into several training modules and include three interactive learning scenarios. The training modules include:

Know About Family Violence in Canada Creating Safety Recognizing and Responding Safely to Child Maltreatment Recognizing and Responding Safely to Intimate Partner Violence Voices of those with Lived Experiences of Family Violence

No Intervention: No Training
Students in this arm will not receive access to the training until the end of the pre- and post-training data collection for the Arm 1 group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in perceived knowledge and preparedness, and opinions about family violence as measured by the Modified Provider Readiness to Manage Intimate Partner Violence Survey Items (Modified PREMIS)
Time Frame: Week one (pre-training), and again Week four (post-training)
Changes in self-rated Knowledge/Preparation and Opinions about intimate partner violence and child maltreatment. Perceived preparedness to manage intimate partner violence and child maltreatment (14 items, 7-point Likert scale ranging from "Not Prepared" to "Quite Well Prepared"). Perceived Knowledge about intimate partner violence and child maltreatment (22 items, 7-point Likert scale ranging from "Nothing" to "Very Much"). Opinions about intimate partner violence and child maltreatment (47 items, 4-point Likert scale, ranging from "Strongly Agree" to "Strongly Disagree").
Week one (pre-training), and again Week four (post-training)
Reactions - Interest and Relevancy of Intervention Material
Time Frame: During Weeks two through three - completed during training period
Measurement of participant reactions to training contents, specifically in terms of the learning objectives and relevancy of each individual training module in order to examine engagement and interest. Agreement on whether training modules met their learning objectives, and whether training module content was relevant is measured on a 7-point scale from Strongly Agree to Strongly Disagree.
During Weeks two through three - completed during training period
Changes in VEGA content knowledge
Time Frame: Week one (pre-training), and again Week four (post-training)
Changes in knowledge regarding family violence content in VEGA modules. Content knowledge measure contains 34 multiple choice questions about the VEGA Family Violence Education Resources. Each question has a maximum score of 1, and minimum score of 0, for a total range of 0 to 34.
Week one (pre-training), and again Week four (post-training)
Performing relevant clinical behaviours in clinical settings with clients, as measured by a Behavioural Checklist
Time Frame: One month post-training.
A checklist of a variety of clinically-relevant behaviours that are recommended and suggested as best practice when working with a survivors of family violence. Participants indicate whether or not they have engaged in certain behaviours. Participants may also indicate if they have not had the opportunity to engage in selected behaviours. The checklist covers 72 clinical actions relating to the VEGA family violence resources, with participants being able to select "Yes", "No", or "N/A" for each action performed in the previous 30 days.
One month post-training.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in attitudes towards evidence-based practice and interventions as measured by the Evidence-Based Practice Attitude Scale (EBPAS)
Time Frame: Week one (pre-training), and again Week four (post-training)
Changes ttitudes toward utilizing evidence-based interventions and their importance in professional and clinical settings. Measured with the EBPAS (Evidence-Based Practice Attitude Scale) - fifteen items across four subscales (Requirements, Appeal, Openness, and Divergence) measured on four-point Likert scales ("Not at All" to "To a Very Great Extent").
Week one (pre-training), and again Week four (post-training)
Interview on experiences with the VEGA family resources
Time Frame: One month post-training.
A randomly selected subset of participants will be invited to participate in an interview one month after the training to discuss their opinions on the VEGA Family Violence Education Resources, what they learned (if anything), and how their clinical approaches have changed.
One month post-training.

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Elisa Romano, PhD, Clinical Psychology, University of Ottawa

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)

October 30, 2024

Primary Completion (Estimated)

March 1, 2025

Study Completion (Estimated)

March 1, 2025

Study Registration Dates

First Submitted

September 30, 2024

First Submitted That Met QC Criteria

October 3, 2024

First Posted (Actual)

October 8, 2024

Study Record Updates

Last Update Posted (Estimated)

November 26, 2024

Last Update Submitted That Met QC Criteria

November 23, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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