Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04171206
Other study ID # 031298
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2019
Est. completion date July 15, 2020

Study information

Verified date November 2019
Source University of Sheffield
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This project is designed to develop and test a brief internet-delivered intervention to promote healthy relationships among young adults.


Description:

In spite of the fact that young adults are at an increased risk of experiencing and perpetrating intimate partner violence (IPV), there is a lack of universal and widely accessible prevention programmes targeted at this age group. One of the reasons for this may be that it is difficult to deliver a universal prevention to individuals who are not formally grouped through one organisation, such as employed young adults. Those who are formally grouped, such as university students, are unlikely to take part in a lengthy prevention programme which is not a part of an official curriculum. Therefore, there is a need for widely available, accessible, and efficacious IPV prevention programmes that could be appropriate for all young adults regardless of gender. Since many young adults in contemporary Western societies were exposed to some kind of relationship education in schools, it may be that a brief programme will suffice to further boost their awareness of IPV and reduce IPV perpetration and victimisation risk. Therefore, we propose a brief internet-based intervention, Free From Abuse - The Booster Project, to achieve these objectives. Primary objectives: 1. To investigate the acceptability and feasibility of the internet-delivered intervention to university students (determined using the 1 and 4-week follow-up rates, % of participants who correctly answered control questions assessing compliance); 2. To assess the acceptability and feasibility of the outcome measures as methods to measure effectiveness of the intervention within a definitive trial (determined using % of missing data); 3. To estimate the standard deviation (SD) for the continuous outcomes to inform sample size calculations for a definitive trial. Secondary objective: 1. To evaluate the potential effectiveness of the brief internet-delivered intervention, Free From Abuse - The Booster Project, in increasing recognition of abusive behaviour, as well as reducing acceptance of myths about domestic violence, abuse perpetration, and abuse victimisation among young university students compared with placebo.


Recruitment information / eligibility

Status Completed
Enrollment 148
Est. completion date July 15, 2020
Est. primary completion date March 15, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 24 Years
Eligibility Inclusion Criteria: - Participants must be university students aged between 18-24 years, reside in the UK, have access to a computer and internet connection, and be fluent in English. Exclusion Criteria: - Participants will not be eligible to enrol in the trial if they have visual and/or auditory deficits with regards to watching video clips.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Free From Abuse
Participants in the treatment arm will watch a 15-minute talk given by an adult female survivor of IPV who tells the story of her abusive relationship. After watching the video, participants will read information on 10 signs of an unhealthy relationship. The intervention will take approximately 25 minutes to complete.
Technology and crime
Participants in the placebo control arm will watch a 19-minute talk on technology development and crime. After watching the video, participants will read 10 facts about cyber security. The intervention will take approximately 25 minutes to complete.

Locations

Country Name City State
United Kingdom The University of Sheffield Sheffield

Sponsors (2)

Lead Sponsor Collaborator
University of Sheffield University of Huddersfield

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in recognition of abusive behaviour Recognition of adolescent relationship abuse (ARA) scale (Rothman, Decker, & Silverman, 2006); scores on this 12-item self-report scale range from 12 to 60, with higher scores indicating an increased recognition of abusive behaviour baseline, immediately post intervention - an average of 1 hour, 1 week, 4 weeks
Primary Change in acceptance of myths about domestic violence Domestic Violence Myth Acceptance Scale (DVMAS; Peters, 2008); scores on this 18-item self-report scale range from 18 to 108, with higher scores indicating an increased acceptance of myths about domestic violence baseline, immediately post intervention - an average of 1 hour, 1 week, 4 weeks
Secondary Change in abuse perpetration Safe Dates - Psychological Abuse Perpetration scale (Foshee et al., 1996, 1998); scores on this 14-item self-report scale range from 14 to 56, with higher scores indicating an increased abuse perpetration baseline, 4 weeks
Secondary Change in abuse victimisation 14-item Safe Dates - Psychological Abuse Victimisation scale (Foshee et al., 1996, 1998); scores on this 14-item self-report scale range from 14 to 56, with higher scores indicating an increased abuse victimisation baseline, 4 weeks
See also
  Status Clinical Trial Phase
Completed NCT06284148 - Confidential IPV Screening Tool N/A
Completed NCT04095429 - Expect Respect Middle School Randomized Trial N/A
Recruiting NCT06100679 - Responsible Engaged and Loving (REAL) Fathers Intervention Evaluation N/A
Recruiting NCT05331352 - Attachment Style and Mentalization Impact Among Women Victims of Domestic Violence N/A
Completed NCT05417919 - Solution-oriented Nursing in Violence Against Women (SONVAW) N/A
Completed NCT04625465 - Proximal Effects of Alcohol on Same-Sex Intimate Partner Violence N/A
Not yet recruiting NCT06350383 - Adapting a Low-cost Intimate Partner Violence and Mental Health Response Intervention N/A
Completed NCT03259646 - The IPV Provider Network: Engaging the Health Care Provider Response to Interpersonal Violence Against Women N/A
Not yet recruiting NCT06124950 - A Couple-based Gender-transformative Intervention on IPV Against Infertile Women N/A
Not yet recruiting NCT06330753 - Synergy Between Patient and Clinician: Using a Trauma-Informed Care Plan N/A
Not yet recruiting NCT05310656 - Evaluation of the Impact of the Empowerment Program on Sheltered Battered Women N/A
Recruiting NCT03623555 - Applied Social Neuroscience: the Building Resilience Among Women Project
Recruiting NCT05608421 - 1MoreStep: An Intervention to Increase HIV Care Engagement and Reduce Intimate Partner Violence Among Black Women Living With HIV N/A
Recruiting NCT05609786 - Dissemination and Implementation of a Web-based Relationship Safety App, myPlanKenya, for Women at Risk for Intimate Partner Violence in Nairobi, Kenya N/A
Recruiting NCT06001307 - Supporting Trans Affirmation, Relationships, and Sex, Phase 3 N/A
Recruiting NCT05768217 - Community Resiliency Collective Efficacy Intervention N/A
Completed NCT04950686 - Study of Long-term Efficacy and Mechanisms Underlying the Impact of a Web-based Sexual and Relationship Health Promotion Program With Young Adult Community College Students N/A
Completed NCT03539315 - Adaptation and Testing of the Addressing Reproductive Coercion in HEalth Settings (ARCHES) Intervention in Bangladesh N/A
Recruiting NCT03498638 - Feasibility Study of Couple Therapy Treatment for Situational Couple Violence N/A
Recruiting NCT04098276 - It's WeWomen Plus Intervention for Health, Safety and Empowerment N/A