NDARC trial to address hidden epidemic of child and adolescent trauma

Image - NDARC trial to address hidden epidemic of child and adolescent trauma
Date Published:
5 Jun 2018
Contact person:
Morgaine Wallace-Steele
Phone:
(02) 9385 0124

Researchers from the National Drug and Alcohol Research Centre (NDARC) at UNSW Sydney are conducting a world-first trial of integrated treatment for post-traumatic stress disorder (PTSD) and alcohol or drug use in adolescents aged 12-18 years.

PTSD and problematic substance use are debilitating conditions that frequently co-occur, with onset typical during adolescence.

It is estimated that 80 percent of adolescents have experienced at least one traumatic event and one in seven suffer from PTSD. For 50 percent of these young people, their PTSD is further complicated by alcohol or drug use, which often occurs as a consequence of repeated ‘self-medication’ for symptoms of traumatic stress.

Associate Professor Katherine Mills said traumas include a wide range of experiences, including physical and sexual assault, violence, accidents, and natural disasters.

“We know that adolescence is a formative developmental window when young people are particularly vulnerable to the impact of trauma, PTSD and substance use,” Associate Professor Mills said.

“Despite this, the vast majority of young people do not receive treatment for these conditions until later in life, if at all.

“Traditional approaches treat PTSD and substance use in adolescents separately, but research findings from our group and others highlight the importance of an integrated approach where one clinician treats both conditions at the same time.”

Currently, there are no evidence-based treatments for adolescents with co-occurring PTSD and substance use.

In a world-first, NDARC researchers will conduct a randomised controlled trial (RCT) of a new integrated cognitive behavioural therapy called COPE-A.

COPE-A has been adapted from an effective adult program that was found to reduce the severity of PTSD symptoms when compared to traditional care and significantly reduce the likelihood of a PTSD diagnosis at follow-up.

COPE-A will be compared to Person-Centred Therapy (PCT), which adopts a supportive counselling approach and has also been shown to produce improvements in substance use and PTSD among adults. In the current trial, both therapies have been specifically tailored to meet the developmental needs of adolescents.

“Eligible young people will be randomly allocated to receive one of these therapies and all participants will receive treatment, which includes up to 16 sessions with a psychologist,” Associate Professor Mills said.

“Research focused on the development of new treatments for adolescents is of paramount public health importance and through this trial we hope to improve our understanding of how best to treat young people who are experiencing traumatic stress and using alcohol or other drugs.”

Recruitment for the trial is now open. For more information, or to refer a young person, please visit the COPE-A website.

A webinar presented by Associate Professor Mills and Dr Natalie Peach is available online now: Post-traumatic stress disorder and substance use. Promising new treatments for adults and adolescents.

Media contacts:

Morgaine Wallace-Steele: (02) 9385 0124| 0432 894 776 | m.wallace-steele@unsw.edu.au
Marion Downey: (02) 9385 0333| 0401 713 850 | m.downey@unsw.edu.au

After expressing interest in the trial, the young person will be contacted by a staff member who will conduct a brief interview to assess their eligibility to participate. Some of the key criteria are as follows:

Participants must:

  • Be aged 12-18 years
  • Have had exposure to at least one traumatic event
  • Be experiencing symptoms of PTSD
  • Have used alcohol or other drugs in the past month and have a history of problematic use
  • Be fluent in English

Key information for participants:

  • Eligible participants will be randomly allocated to receive COPE-A or Person-Centred Therapy (PCT).
  • Both treatments consist of up to 16 sessions with a psychologist, as well as up to four optional caregiver information sessions.
  • Sessions are once a week and take approximately 60-90 minutes.
  • All sessions are provided free of charge and will be delivered in the Sydney area, at the University of New South Wales (UNSW) in Randwick or at locations convenient to participants.
  • Participants are able to continue seeing their regular clinician while in the trial.
  • All information provided will remain anonymous and confidential.