CClinicalTrials.gg
Status unknownNCT02394990Updated Mar 31, 2015

Violence Brief Intervention Pilot v1.1

An interventional study of Violence Brief Intervention and ABI in Alcohol Consumption, Violence and Facial Injuries, sponsored by NHS Greater Glasgow and Clyde. Status unknown at 1 site in United Kingdom. Open to male participants aged 16 Years to 28 Years. Per ClinicalTrials.gov, last updated 2015-03-31.

Sponsored by NHS Greater Glasgow and Clyde · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Mar 2015), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
300
Allocation
Randomized
Ages
16 Years to 28 Years
Sex
Male
01

Study 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 This will not be withdrawn.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.

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Conditions studied

  • Alcohol Consumption
  • Violence
  • Facial Injuries

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03

In context

Alcohol Drinking

925 studies on the registry are indexed under Alcohol Drinking; 172 are open to participants now.

This study's planned enrollment of 300 is above the median of 108 across 802 interventional studies indexed under Alcohol Drinking.

Browse Alcohol Drinking studies →

Lead sponsor

NHS Greater Glasgow and Clyde is the lead sponsor of 215 studies on the registry; 39 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 28 Years
Sexes eligible
Male
Accepts 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

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
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
300 participants (estimated)

Study arms

  • Experimental
    Violence Brief Intervention

    Participants receive a standard of care brief motivational intervention (BMI) to address alcohol consumption (ABI) based on self reported use and their relationship between consumption and behavior, followed by an additional BMI to address how involvement in violence (VBI) impacts their life, relationship to social norms, and strategies to avoid violence.

    Behavioral: Violence Brief Intervention

  • Active comparator
    Control

    Participants receive only ABI

    Behavioral: ABI

Interventions

  • BehavioralViolence Brief Intervention

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

    Also known as: VBI

  • BehavioralABI
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What researchers measure

Primary outcomes

  1. Re-admission for trauma injury

    Time frame: 12 months post-intervention

  2. Named in police crime report as perpetrator, victim or witness of violence

    Time frame: 12 months post-intervention

  3. Attitudes toward violence

    Time frame: 1, 3 and 6 months post intervention

Secondary outcomes

  1. Participant relationships to alcohol measured using the Fast Alcohol screening test

    Time frame: Baseline

07

Study locations

1 of 1 sites recruiting
  • Department of Oral and Maxillofacial Surgery, Southern General Hospital
    Glasgow, G51 4QS, United Kingdom
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 31, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02394990
Lead sponsor
NHS Greater Glasgow and Clyde
Collaborators
University of Glasgow
Responsible party
Sponsor
First posted
Mar 20, 2015
Start date
Mar 2015
Primary completion
Mar 2016 (estimated)
Completion
Mar 2016 (estimated)
Last update
Mar 31, 2015

Study contacts

Christine Goodall, BDS, PhD
Contact
christine.goodall@glasgow.ac.uk
441412119655
Christine Goodall, BDS, PhD
principal investigator · University of Glasgow

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2015. You cannot join it, but the record below documents what was studied.

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