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Personalised and contingency-based interventions for suicide risk.

Personalised and contingency-based interventions for suicide risk: A cluster randomised controlled trial in an Australian veteran community sample.

Status
Withdrawn
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12621001680853
Enrollment
2000
Registered
2021-12-09
Start date
2022-02-01
Completion date
2022-09-30
Last updated
2023-04-24

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

Conditions

None listed

Brief summary

The aim of this study is to test the effectiveness of a personalised and contingency-based approach to managing individuals at risk of suicide in an Australian veteran community sample. The study will use a cluster randomised control design to compare the effectiveness of a personalised and contingency-based approach to treatment as usual (TAU), for reducing distress, decreasing suicidal ideation and behaviours, increasing treatment engagement and improving safety plan quality and connection to supports. The study will also explore whether a) the change in safety plan quality (post intervention – baseline) is greater for those receiving a personalised and contingency-based intervention compared to TAU, b) whether the change in safety plan quality partially mediates treatment response and c) whether the effectiveness of implementation for clinicians incorporating a personalised and contingency-based intervention improves treatment response. For this research, the personalised and contingency-based approach being utilised is the SafeSide Framework for Recovery-Oriented Suicide Prevention. Noteworthy in this study design, the clinician training, not the client’s treatment is randomised. Clinicians will be grouped according to location and randomised to commence training at two time points, six months apart. A comparison of intervention effect and control condition between groups will occur during this period, as well as an assessment of implementation effectiveness.

Interventions

Open Arms - Veterans & Families Counselling (Open Arms) is Australia’s leading provider of high quality, nationally accredited, mental health care for veterans and their families. A key service delivery arm of the Department of Veterans’ Affairs, Open Arms provides free and confidential 24-hour counselling and support. Any current and former Australian Defence Force (ADF) member with one day continuous full-time service can receive support through Open Arms, as can their partners and children.

Open Arms - Veterans & Families Counselling (Open Arms) is Australia’s leading provider of high quality, nationally accredited, mental health care for veterans and their families. A key service delivery arm of the Department of Veterans’ Affairs, Open Arms provides free and confidential 24-hour counselling and support. Any current and former Australian Defence Force (ADF) member with one day continuous full-time service can receive support through Open Arms, as can their partners and children. There is no limit on the number of counselling sessions a person receives through Open Arms, support is provided based on clinical need. Open Arms services include: counselling for individuals, couples and families; care coordination for clients with more complex needs; group programs to develop skills and enhance support; lived experience mental health peer support; after-hours telephone counselling and telehealth; mental health literacy and suicide awareness training; information, education and self-help resources; and referrals to other services or specialist treatment programs, as needed. Clients receiving care from an Open Arms clinician (psychologist or accredited mental health social worker), in the intervention condition, will be assessed for suicide risk utilising the Open Arms Risk Assessment (OARA) template. The OARA is a tool developed by Open Arms to deliver a personalised and contingency-based response to suicide risk. The template contains the Columbia Suicide Severity Rating Scale (C-SSRS) and standardised assessment questions related to risk of harm to self. The OARA tool supports clinicians in the development of a risk formulation and safety plan. For this research, the personalised and contingency-based approach being utilised is the SafeSide Framework for Recovery-Oriented Suicide Prevention (SafeSide). SafeSide is a formulation-based approach to suicide risk assessment with a focus on planning rather than prediction. It is widely accepted that suicide cannot be predicted, therefore this model aims to assess the vulnerability and strengths of individual clients; and develop plans to mitigate risk and extend supports. The Framework unites mental health professionals through a shared framework that focusses on four core goals of person-centred suicide care: Connect – Assess – Respond – Extend. Risk formulation is an approach to suicide risk assessment, which comprises a concise synthesis of empirically based suicide risk information regarding a client’s immediate distress and resources at a specific time and place. The goal of this synthesis is not to predict behaviour but to promote communication and collaboration among professionals, client, and families to reduce risk in the short and long term. This study is a cluster randomised controlled trial (CRCT) whereby clinicians are randomly allocated to two conditions, a) standard care, without training (control group), and b) standard care, with training and implementation support (intervention group). Clinician and client outcomes between groups, and within groups, will be compared. InPlace Learning is SafeSide’s approach to sustainable, engaging work-force training by combining video-based instruction with live group interaction. Video instruction is delivered by Dr Pisani and co-led by lived experience consultant and patient advocate, Kristina Mossgraber. Open Arms will provide the core training online to clinicians across two half day sessions. Upon completion of the training: • Clinicians will be able to name three foundational goals for forming productive collaborations with clients and their families to address suicide risk. • Given a scenario, clinicians will be able to communicate a prevention-oriented risk formulation, orally and in writing. • Clinicians will be able to name four key domains to document in a short-term response to suicide risk to facilitate care and minimize liability. • Clinicians will be able to state at least two steps their own organization or program can take to strengthen care transitions. Following training, clinicians join the SafeSide community of practice which provides them access to expert supervision during monthly Office Hours, as well as regular updates, new modules and refreshers throughout the year.

Sponsors

Open Arms - Veterans & Families Counselling
Lead SponsorGovernment body

Study design

Allocation
Randomised controlled trial
Intervention model
Other
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Data for the following groups will be collected as part of standard care: • Clients aged over 18 years with a positive screen for suicide risk. • Clinicians and mental health peer workers.

Exclusion criteria

Data will be excluded for clients who have not provided informed consent.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026