Caring Text Messages for Suicide Prevention
(SUNDANCE Trial)
Trial Summary
What is the purpose of this trial?
This study compares the effectiveness of a program to detect and manage suicide risk among American-Indian and Alaska Native (AI/AN) youth. Half of the participants will receive caring text messages to reduce suicidal thoughts, attempts, and hospitalizations and to increase engagement, social connectedness, and resilience in at-risk youth. The other half will receive usual care that does not include the caring text messages.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications.
What data supports the effectiveness of the treatment SBIRT+12, SBIRT with 12 months of caring text messages, SBIRT+12, SBIRT+Usual Care, SBIRT+Usual Care, Screening, Brief Intervention, and Referral to Treatment with usual care?
SBIRT (Screening, Brief Intervention, and Referral to Treatment) is effective in reducing risky alcohol use and improving follow-up care when combined with motivational interviewing, which suggests that similar supportive approaches like caring text messages could enhance its effectiveness in suicide prevention.12345
Is SBIRT with caring text messages safe for humans?
How is the SBIRT+12 treatment for suicide prevention different from other treatments?
The SBIRT+12 treatment is unique because it combines the Screening, Brief Intervention, and Referral to Treatment (SBIRT) approach with 12 months of caring text messages, providing ongoing support and connection, which is not typically part of standard care. This method leverages the accessibility and cost-effectiveness of text messages to maintain contact and express care, aiming to reduce suicide risk.89101112
Research Team
Spero Manson, PhD
Principal Investigator
University of Colorado, Denver
Dedra Buchwald, MD
Principal Investigator
University of Washington
Eligibility Criteria
This trial is for American Indian or Alaska Native youth who can read and speak English, have a text-enabled mobile phone, and are at mild to severe risk of suicidality but not in immediate danger of self-harm. They must be able to consent and participate voluntarily.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
SBIRT Intervention
Participants receive the SBIRT model intervention, with the experimental group receiving additional caring text messages for 12 months
Follow-up
Participants are monitored for changes in hospitalizations, suicidal ideation, suicide attempts, and social connectedness
Treatment Details
Interventions
- SBIRT+12
- SBIRT+Usual Care
SBIRT+12 is already approved in United States for the following indications:
- Suicide prevention in American Indian and Alaska Native youth
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Colorado, Denver
Lead Sponsor
University of New Mexico
Collaborator
National Institute of Mental Health (NIMH)
Collaborator
Washington State University
Collaborator