Suicidal Ideation clinical trials at UCLA

3 in progress, 2 open to eligible people

Showing trials for

  • Assessing Improvements in Mood and Sleep Trial

    open to eligible people ages 55 years and up

    This is a multi-site randomized control trial involving people age 55+ years who have current depression symptoms plus another suicide risk indicator (either current suicidal ideation or a past history of attempt). Our goal is evaluate which of two different approaches works best to improve things like trouble sleeping, bad moods, and any suicidality. Participants will complete diagnostic interviews, self-report scales, and wear an actigraphy device for the 8 weeks starting at the baseline visit.

    Los Angeles 5368361, California 5332921 and other locations

  • SAFETY-A for Promoting Equity in Suicide Prevention Outcomes in Schools

    open to eligible people ages 11 years and up

    This study will adapt Safe Alternatives For Teens and Youth - Acute (SAFETY-A) for implementation in low-resourced school districts to reduce racial/ethnic disparities in mental health service use (MHS) following identification of suicide risk in youth. SAFETY-A will be adapted to fit the organizational context of school districts and to reduce mistrust of MHS, internalized stigma, and concealment of youth emotional distress that arise in school suicide risk assessments with Asian American and Latinx students. Following a prototyping case series, a feasibility trial will assign four districts to the timing of SAFETY-A implementation to generate preliminary data on feasibility and impacts on proposed mechanisms and youth MHS utilization and clinical outcomes across racial/ethnic groups.

    Los Angeles 5368361, California 5332921

  • acTBS Treatment for Inpatient Subjects With Suicidality

    Sorry, in progress, not accepting new patients

    This is a pilot study to analyze the benefit of accelerated continuous Transcranial magnetic stimulation for inpatient subjects suffering with suicidal ideation. This study will enroll 40 inpatient subjects recruited from the Resnick Neuropsychiatric hospital. Subjects will be blinded and randomized to active or sham TMS treatment and will receive up to 5 assigned treatments per day. Subjects will also be asked to complete mood surveys throughout their participation. Participation in this study will last 7-10 days depending on scheduling.

    Los Angeles 5368361, California 5332921

Our lead scientists for Suicidal Ideation research studies include .

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