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| ID | Type | Description | Link |
|---|---|---|---|
| SP-2020C3-210 | Other Grant/Funding Number | PCORI |
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Lack of eligible participants during study time period
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| Name | Class |
|---|---|
| Patient-Centered Outcomes Research Institute | OTHER |
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The aim of this pilot study is to reduce suicide among sexual and gender diverse youth ages 18-24 years old. This pilot study will compare two brief suicide prevention interventions that have been adapted for use with this population to use in primary care via telehealth and will recruit 40 youth from 4-6 primary care clinics in the Dallas and Austin, Texas metropolitan areas. Each clinic will be randomly assigned to deliver one of the two study interventions.
This is a cluster randomized study focused on youth suicide prevention which will recruit 40 youth from four primary care clinics serving sexual and gender diverse young adults in the Dallas and Austin, TX metropolitan areas. Each clinic will recruit 10 youth. Two clinics will be randomly assigned to deliver each of the two study interventions. The interventions are adapted versions of two existing, brief suicide prevention interventions: 1) Suicidal Teens Accessing Treatment after an ED Visit (STAT-ED) is a brief intervention based on motivational interviewing that focuses on mental health care seeking behavior, problem-solving, and referrals plus brief case management; and 2) Youth-Nominated Support Team for Suicidal Adolescents (YST-II) is a brief intervention developed for youth who have been psychiatrically hospitalized due to a suicide attempt or suicidal ideation. The revised interventions will be called STAT-PC and YST-III. For YST III, participants will identify 1-2 supportive adults from their lives who agree to provide ongoing contact and support. The interventions will last two months. Primary and secondary outcome assessments will be done at baseline and/or at 2 months.
To be eligible, participants must report risk factors for suicide based on screening questions that will be implemented in our primary clinic sites.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Suicidal Teens Accessing Treatment - Primary Care (STAT-PC) | Experimental | This group will undergo a brief, suicide prevention intervention based on motivational interviewing that focuses on mental health care seeking behavior, problem-solving, and referrals plus brief case management |
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| Youth-Nominated Support Team (YST-III) | Experimental | This group will undergo a brief, suicide prevention intervention originally developed for youth who have been psychiatrically hospitalized due to a suicide attempt or suicidal ideation that has been adapted |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| STAT-PC | Other | STAT-PC is an adapted version of Suicidal Teens Accessing Treatment after an ED Visit (STAT-ED). It is a brief intervention based on motivational interviewing (MI) that focuses on mental health care seeking behavior, problem-solving, and referrals plus brief case management (2-3 follow-up calls). The intervention will consist of an initial session with the youth focusing on accessing mental health care plus two case management calls. The interventionist will also be available to assist with referrals for connection to other services later during the study period as needed for up to two months. The intervention may include contact with the youth's mental health provider to make sure linkages are made. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in suicidal ideation as measured by ASIQ | Change in suicidal ideation is measured by Adult Suicidal Ideation Questionnaire (ASIQ). It is a 25-item, self-report assessment of suicidal thoughts designed specifically for adult populations. Possible scores range from 1 (Not at All) to 6 (Extreme), with lower scores indicating less severe suicidal ideation (better outcome) | Baseline, 2 months |
| Measure | Description | Time Frame |
|---|---|---|
| Change in number of mental healthcare service utilization as measured by ED-STARS mental health service utilization check list | Change in number of mental healthcare service utilization is measured by Emergency Department Screen for Teens at Risk for Suicide (ED-STARS) mental health service utilization check list which will be used to assess the number of different types of mental health services that participants receive including inpatient psychiatric services, emergency department visits, medication management, and psychotherapy/counseling. |
| Measure | Description | Time Frame |
|---|---|---|
| Number of participants who had access to means for suicide at baseline | This is a descriptive measure with patient reported Yes/ No responses and if yes, to categorize the means for suicide. | Baseline |
| Number of participants who had access to means for suicide at 2 months |
Inclusion Criteria:
Exclusion Criteria:
Those who are excluded will be provided with referrals for treatment services.
To enroll, participants must identify as a sexual or gender minority individual (i.e., LGBTQ+) and be a patient of the one the clinic sites
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| Name | Affiliation | Role |
|---|---|---|
| Elizabeth Arnold, PhD | University of Texas Southwestern Medical Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| UT Southwestern Medical Center | Dallas | Texas | 75390 | United States |
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| ID | Term |
|---|---|
| D059020 | Suicidal Ideation |
| D003863 | Depression |
| D013405 | Suicide |
| D003075 | Coitus |
| ID | Term |
|---|---|
| D016728 | Self-Injurious Behavior |
| D001526 | Behavioral Symptoms |
| D001519 | Behavior |
| D012725 | Sexual Behavior |
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| YST-III | Other | YST-III is an adapted version of Youth-Nominated Support Team for Suicidal Adolescents (YST-II). The intervention is a brief intervention developed for youth who have been psychiatrically hospitalized due to a suicide attempt or suicidal ideation (SI). Participants will nominate 1-2 supportive adults (age 18 and older) from their lives who agree to provide ongoing contact and support for up to 2 months. YST-III will include an introductory session with the youth who will nominate their support persons plus referrals for mental health services. The support persons will receive training on how to best support their youth partner and then ongoing calls to support them in working with their youth partner for up to 2 months. |
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| Baseline, 2 months |
| Number of past 2 months suicide attempts at baseline | Past 2 months suicide attempts is measured by suicide attempt question from the Columbia-Suicide Severity Rating Scale (CSSRS) which will assess the number of suicide attempts. | Baseline |
| Number of lifetime suicide attempts at baseline | Suicide attempts is measured by suicide attempt question from the Columbia-Suicide Severity Rating Scale (CSSRS) which will assess the number of suicide attempts. | Baseline |
| Number of suicide attempts at 2 months | Suicide attempts is measured by suicide attempt questions from the Columbia-Suicide Severity Rating Scale (CSSRS) which will assess the number of suicide attempts. | 2 months |
| Change in depressive symptoms as measured by CESD-R | Change in depressive symptoms is measured by Center for Epidemiologic Studies Depression Scale-Revised (CESD-R) which is a 20-item measure of depression that assesses the duration symptoms across a period of two weeks. Possible scores range from 0-60, with lower scores indicating less depressive symptoms (better outcome). | Baseline, 2 months |
| Change in social support as measured by MSPSS | Change in social support is measured by Multidimensional Scale of Perceived Social Support (MSPSS) which is a 12-item measure with three subscales that assesses family, friend, and significant other support. Response categories are on a 7-point Likert-scale from 1=very strongly disagree to 7=very strongly agree. The overall score will be used to assess change. The 12-item MSPSS scale has a mean continuous score ranging from 1-84. Higher scores indicate greater perceived social support (better outcome). | Baseline, 2 months |
| Change in internalized stigma as measured by ITS-adapted | Change in internalized stigma is measured by Internalized Transphobia Scale (ITS) - adapted. Internalized stigma will be measured by an adapted version of the Internalized Transphobia Scale (ITS). The measure consists of 22 questions. Possible score ranges from 1-4 with lower scores indicating less internalized stigma (better outcome) | Baseline, 2 months |
| Number of deaths by suicide at 2 months | The data on any reported deaths due to suicide during the study period will be collected. | 2 months |
This is a descriptive measure with patient reported Yes/ No responses and if yes, to categorize the means for suicide. |
| 2 months |
| Proportion of participants who screened and met criteria | Proportion of participants who screened and met criteria is obtained at the last day of the study recruitment period. | Last day of study recruitment period (approx. week 14) |
| Proportion of participants who enrolled in the study | Proportion of participants who enrolled in the study is obtained at the last day of the study recruitment period. | Last day of study recruitment period (approx. week 14) |
| Number of participants who decide not to participate | For potential study candidates who decide not to participate, refusal reason will be logged. | 2 months post-intervention |
| Intervention acceptability | Intervention acceptability will be measured by asking participants to rate the extent to which they agree with 4 statements about the study intervention received on a scale of 1 to 4 where 1 is strongly disagree and 4 is strongly agree | 1 month post-intervention |
| Study feasibility | Study feasibility will be measured by asking participants to rate the extent to which they agree with 5 statements about the study on a scale of 1 to 4 where 1 is strongly disagree and 4 is strongly agree. | 1 month post-intervention |