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Violence Brief Intervention Pilot v1.1

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NHS Trust

Status

Unknown

Conditions

Alcohol Consumption
Facial Injuries
Violence

Treatments

Behavioral: ABI
Behavioral: Violence Brief Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT02394990
GN14NU421

Details and patient eligibility

About

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 This will not be withdrawn.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.

Enrollment

300 estimated patients

Sex

Male

Ages

16 to 28 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

300 participants in 2 patient groups

Violence Brief Intervention
Experimental group
Description:
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.
Treatment:
Behavioral: Violence Brief Intervention
Control
Active Comparator group
Description:
Participants receive only ABI
Treatment:
Behavioral: ABI

Trial contacts and locations

1

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Central trial contact

Christine Goodall, BDS, PhD

Data sourced from clinicaltrials.gov

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