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Violence Brief Intervention Pilot v1.1

A Randomised Controlled Trial to Evaluate a Violence Brief Intervention (VBI) for Adult Male Patients With Facial Injuries Sustained as a Result of Interpersonal Violence

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02394990
Enrollment
300
Registered
2015-03-20
Start date
2015-03-31
Completion date
2016-03-31
Last updated
2015-03-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcohol Consumption, Facial Injuries, Violence

Brief summary

This study is a randomised controlled trial of a new brief intervention with young (16-29) adult male patients who have a facial injury sustained as a result of interpersonal violence (fighting or assaults). It will be undertaken at the Maxillofacial outpatient trauma clinic at the Southern General Hospital, Glasgow. The major risk factors associated with facial injury in Scotland are male gender, young age, interpersonal violence and alcohol. Previous research with facial injury patients attending this clinic has shown that an Alcohol Brief Intervention (ABI) is effective in helping reduce alcohol consumption, so all patients are now offered ABI as standard practice. ABI is delivered by trained nurses from Addiction Services. This will not be withdrawn. In addition we wish to offer some patients a Violence Brief Intervention (VBI). This will be delivered by the same nurses who deliver the ABI. The study is randomised so only those selected at random will receive this extra intervention and all others will receive treatment as normal (ABI only). VBI is a short psychological intervention which uses Brief Motivational Interviewing (BMI) to encourage reflection of involvement in violence and consideration of strategies to avoid future violence. The intervention also compares participants' attitudes towards violence to those of their peers. The intervention takes about 15 minutes, and patients will be involved for an additional 30-45 minutes longer than normal when they attend the clinic, including consent and baseline data collection. Patients will be followed up by telephone at 1, 3 and 6 months, and asked a suite of questions which will take approximately 15 minutes on each occasion. We wish to determine whether a VBI of this type has any effect on attitudes to violence or propensity for involvement in violence or on reinjury, examined through self report measures and routinely collected health and criminal justice data at 12 months post intervention.

Interventions

BEHAVIORALViolence Brief Intervention

Strategies for self assessment of consequences of violent behavior and strategies for avoidance of violence

BEHAVIORALABI

Sponsors

University of Glasgow
CollaboratorOTHER
NHS Greater Glasgow and Clyde
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
16 Years to 28 Years
Healthy volunteers
No

Inclusion criteria

* facial trauma patients * Facial injury resulting from interpersonal violence (whether victim or perpetrator) * Able to give informed consent * Willing to commit to screening intervention and follow up programme lasting 6 months * Within 28 days of injury * Willing to provide either a contact telephone number or email address for the followup surveys * Participants score ≥ 3/16 on the Fast Alcohol Screening Test (FAST)

Exclusion criteria

* Unable to give informed e.g. adults with dementia, severe psychiatric problems, patients with learning difficulties who cannot consent for themselves * Under 16 or over 29 years of age. * Injury more than 28 days old * Participants score ≤ 2/16 on the FAST measure

Design outcomes

Primary

MeasureTime frame
Re-admission for trauma injury12 months post-intervention
Named in police crime report as perpetrator, victim or witness of violence12 months post-intervention
Attitudes toward violence1, 3 and 6 months post intervention

Secondary

MeasureTime frame
Participant relationships to alcohol measured using the Fast Alcohol screening testBaseline

Countries

United Kingdom

Contacts

Primary ContactChristine Goodall, BDS, PhD
christine.goodall@glasgow.ac.uk441412119655

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026