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Clinical Trials/NCT03136094
NCT03136094
Recruiting
Not Applicable

Collaborative Hub to Reduce the Burden of Suicide Among Urban American Indian and Alaska Native Young Adults

University of Colorado, Denver1 site in 1 country698 target enrollmentMarch 15, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Suicide Prevention
Sponsor
University of Colorado, Denver
Enrollment
698
Locations
1
Primary Endpoint
Change in Suicidal Ideation
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

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.

Detailed Description

The study, "Suicide in Urban Natives: Detection and Networks to Combat Events," builds on Screening, Brief Intervention and Referral to treatment (SBIRT), carried out through the primary care setting, to detect and manage suicide risk. This approach is multilevel, targeting both the healthcare system and the individual, and links screening to existing mobile phone technologies shown to promote resilience and to tap the protective benefits of social connectedness. This Collaborative Hub will conduct a randomized control trial that compares the effectiveness of enhancing these SBIRT programs by sending caring text messages to reduce suicidal ideation, attempts, and hospitalizations, and to increase engagement, social connectedness, and resilience. The Investigators' long-term goal is to disseminate and translate the lessons learned into practical policy, organizational changes, and preventive innovations that optimize patient-centered health outcomes and ultimately reduce or eliminate the dramatic and tragic suicide-related health disparities among urban AI/AN youth and young adults.

Registry
clinicaltrials.gov
Start Date
March 15, 2020
End Date
May 31, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Self-identify as American Indian or Alaska Native;
  • Screen positive for mild, moderate, or severe risk of suicidality (referred by a clinical provider);
  • Have a text-enabled mobile phone;
  • Willing to be contacted by text;
  • Able to participate voluntarily;
  • Speak and read English;
  • Cognitively able to independently provide written informed consent

Exclusion Criteria

  • Under age 18
  • In danger of imminent self-harm;
  • Hospitalized

Outcomes

Primary Outcomes

Change in Suicidal Ideation

Time Frame: Baseline, 6 months, 12 months

The 15-item Suicidal Ideation Questionnaire Jr. assesses frequency of suicidal thoughts in the past month. Item content ranges from general thoughts of death and wishes that one were dead to specific thoughts of self-injurious behavior. Responses are on a 7-point scale ranging from never to almost daily. Items are summed for a total score (range 0-90).

Change in Self-Reported Suicide Attempts

Time Frame: Baseline, 6 months, 12 months

The investigators will use the interviewer-administered Suicide Attempt and Self-Injury Count to assess the method, intent, treatment received, and lethality for all suicide attempts over the respondent's lifetime.

Change in Hospitalizations and Behavioral Health Treatment

Time Frame: Baseline, 6 months, 12 months

The investigators will assess self-reported hospitalizations over the previous 12 months with a measure of health service use previously applied to AI/ANs. It captures information on inpatient and outpatient medical care, emergency room visits, and use of traditional practices.

Secondary Outcomes

  • Change in Social Connectedness(Baseline, 6 months, 12 months)
  • SBIRT Retention and Uptake of Referral to Therapy(6 months, 12 months)

Study Sites (1)

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