A Pre-post Study of a Lethal Means Safety Planning Intervention for Youth at Elevated Suicide Risk in the Emergency Department
NCT07916792, Not applicable, Not yet recruiting, University of Colorado, Denver
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | A Pre-post Study of a Lethal Means Safety Planning Intervention for Youth at Elevated Suicide Risk in the Emergency Department | ClinicalTrials.gov |
| NCT number | NCT07916792 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 200 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | University of Colorado, Denver | ClinicalTrials.gov |
| Conditions | Suicidal Ideas, Suicidal Ideation, Suicidal Thoughts, Firearm Safety | ClinicalTrials.gov |
| Interventions | TEEN LENS, Usual Care | ClinicalTrials.gov |
| First posted | 2026-11-04 | ClinicalTrials.gov |
| Last updated | 2026-11-06 | ClinicalTrials.gov |
Registered outcomes 6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Acceptability among teens | Within 48 hours of receipt of care (intervention or control). | Acceptability among teens during the intervention versus control period using the composite score from the adapted validated Client Satisfaction Questionnaire (CSQ-8), where higher scores indicate increased acceptability. | ClinicalTrials.gov |
| Secondary | Acceptability among caregivers | Within 48 hours of receipt of care (intervention or control). | Acceptability among caregivers during the intervention versus control period using the composite score from the adapted validated Client Satisfaction Questionnaire (CSQ-8), where higher scores indicate increased acceptability. | ClinicalTrials.gov |
| Secondary | Provider perceived acceptability | From start of the intervention period until end of the intervention period (6 months). | Provider perceived acceptability of using TEEN LENS ED using the validated Acceptability of Intervention Measure (AIM), a composite score where higher scores indicate higher acceptability. | ClinicalTrials.gov |
| Secondary | Provider perceived appropriateness | From start of the intervention period until end of the intervention period (6 months). | Provider perceived appropriateness using the validated Intervention Appropriateness Measure (IAM), a composite score where higher scores indicate higher appropriateness. | ClinicalTrials.gov |
| Secondary | Provider perceived feasibility | From start of the intervention period until end of the intervention period (6 months). | Provider perceived feasibility using the validated Feasibility of Intervention Measure (FIM), a composite score where higher scores indicate higher feasibility. | ClinicalTrials.gov |
| Secondary | Feasibility of follow up | From enrollment to follow up at 2 months. | Proportion of participants who complete baseline surveys that complete follow up. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 1
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|---|---|---|---|---|---|
| K23HD114903 | TEEN LENS ED: TEen ENgaged LEthal meaNS planning for the Emergency Department | HAASZ, MAYA | UNIVERSITY OF COLORADO DENVER | EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT | 2024 to 2025 | NIH RePORTER |
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)