SPI+ and CAMS for Suicide Prevention in Teens
(ASSIST Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to improve the management of suicide risk in teens by testing two treatments: Collaborative Assessment and Management of Suicidality (CAMS) and Safety Planning Intervention+ (SPI+). CAMS involves working with teens to address the issues that lead to suicidal feelings, while SPI+ focuses on creating personalized plans to handle suicidal crises. Teens admitted to acute care due to suicidal thoughts or actions might be suitable candidates for this trial. As an unphased trial, this study offers teens the chance to contribute to important research that could enhance suicide prevention strategies.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that the Collaborative Assessment and Management of Suicidality (CAMS) effectively reduces suicidal thoughts. Studies have found it to be both effective and safe for individuals experiencing serious self-harm thoughts. No major safety issues have been reported, indicating CAMS is well-tolerated.
For the Safety Planning Intervention+ (SPI+), less research is available. However, it helps individuals by providing coping strategies and support resources during a crisis. Reports of negative effects from using SPI+ are insignificant, suggesting it is generally safe for teenagers.
Both CAMS and SPI+ aim to reduce suicide risk and appear safe based on current research.12345Why are researchers excited about this trial's treatments?
Researchers are excited about the treatments for suicide prevention in teens because they offer a fresh approach to managing suicidal thoughts and behaviors. Unlike traditional methods that might focus solely on crisis intervention or medication, CAMS involves a collaborative process where therapists work together with teens to identify and address the specific problems driving their suicidal thoughts. This method empowers teens to play a central role in their recovery. On the other hand, SPI+ provides a structured safety plan that helps teens recognize early warning signs and implement personalized strategies during a crisis, potentially leading to quicker and more sustainable outcomes. These approaches offer hope for more tailored and effective solutions in preventing teen suicide.
What evidence suggests that this trial's treatments could be effective for suicide prevention in teens?
In this trial, participants will be assigned to different treatment arms to evaluate their effectiveness in suicide prevention for teens. Research has shown that the Collaborative Assessment and Management of Suicidality (CAMS), one of the treatments in this trial, effectively reduces suicidal thoughts. Studies indicate that people using CAMS have better relationships with their therapists and attempt suicide less often in a short time. CAMS helps by focusing on the specific issues that make someone feel suicidal and works together with them to address these issues.
Another treatment arm in this trial is the Safety Planning Intervention+ (SPI+). Strong support exists for its use in adults, but evidence for its effectiveness in teens is still being gathered. SPI+ involves creating a personalized plan to manage crisis moments, including strategies and contact information for support when feeling at risk. Early results suggest that having a plan ready can be crucial for preventing suicidal behavior in high-risk situations.16789Who Is on the Research Team?
Molly Adrian
Principal Investigator
Seattle Childrens
Are You a Good Fit for This Trial?
This trial is for young people aged 11-17 who are experiencing suicidal thoughts or behaviors and have been admitted to acute care for these reasons. They must be able to give informed consent and understand English well enough for study assessments. It's not open to those with psychosis, intellectual disabilities, autism spectrum disorder, or unstable eating disorders.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive interventions such as CAMS, SPI+, or Treatment As Usual, with a minimum of 4 sessions and a maximum of 8 sessions
Follow-up
Participants are monitored for safety and effectiveness after treatment, with assessments at baseline, 2-week, 1-month, 2-month, 6-month, and 12-month timepoints
What Are the Treatments Tested in This Trial?
Interventions
- Collaborative Assessment and Management of Suicidality (CAMS)
- Safety Planning Intervention+ (SPI+)
- Treatment As Usual
Collaborative Assessment and Management of Suicidality (CAMS) is already approved in United States for the following indications:
- Suicidal ideation
- Suicidal behavior
- Adolescent suicide risk management
Find a Clinic Near You
Who Is Running the Clinical Trial?
Seattle Children's Hospital
Lead Sponsor
Nationwide Children's Hospital
Collaborator