Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05312437 · ClinicalTrials.gov registry record · NA

Clinical Decision Support to Prevent Suicide

A NA study, sponsored by Vanderbilt University Medical Center.

Completed
Registry status
NA
Development phase
596
Enrollment target

NCT05312437: Completed NA study, sponsored by Vanderbilt University Medical Center.

NCT05312437 is a NA study that has completed, run by Vanderbilt University Medical Center. The registered enrollment target is 596 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05312437, a NA study, has completed, sponsored by Vanderbilt University Medical Center.

COMPLETED
Registry status
NA
Development phase
596 participants
Enrollment target

Study Summary

Suicide kills 132 Americans every day. The first step of suicide prevention is risk identification and prognostication. Researchers like this study team have developed and validated predictive models that use routinely collected Electronic Health Record (EHR) data like past diagnoses and medications to predict future suicide attempt risk. The study team's model based in machine learning is known as the Vanderbilt Suicide Attempt and Ideation Likelihood (VSAIL). VSAIL has been validated prospectively and externally to predict suicide attempt risk with a number needed to screen (NNS) of 271 for suicide attempt and 23 for suicidal ideation. NNS is the number of people who need to receive a test result to prevent one outcome - lower NNS is better. This study will evaluate the effectiveness of a Clinical Decision Support System called Vanderbilt Safecourse using VSAIL to prompt a novel Best Practice Advisory (BPA) to prompt face-to-face screening with a validated suicide screening instrument like the Columbia Suicide Severity Rating Scale (CSSRS).

Primary Outcome

Documentation of the validated, brief-version of the Columbia Suicide Severity Rating Scale (https://www.cms.gov/files/document/cssrs-screen-version-instrument.pdf) or recording a binary response "Will screen with alternative method" input by providers into the intervention Best Practice Advisory using a button in the Acknowledge Reason section of the BPA.

Interventions

  • OTHER Interruptive Alert, CDS
  • OTHER Passive Prompt, CDS

Trial Details

FieldValue
Enrollment Target 596 participants
Start Date 2022-08-16
Est. Completion 2023-02-16
Phase NA

What the finished NCT05312437 record still lists

NCT05312437 is an interventional study that assigns participants to a tested intervention. The registered 596 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (58% lower).

The record links to 0 conditions, and to 2 interventions - of which Interruptive Alert, CDS is the first listed.

NCT05312437 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05312437 about?

NCT05312437 is a clinical study titled "Clinical Decision Support to Prevent Suicide". Suicide kills 132 Americans every day. The first step of suicide prevention is risk identification and prognostication. Researchers like this study team have developed and validated predictive models that use routinely collected Electronic Health Record (EHR) data like past diagnoses and medications...

What is the current status of trial NCT05312437?

This trial is currently completed. It is a NA study. The enrollment target is 596 participants. The study started on 2022-08-16. Estimated completion is 2023-02-16.

What interventions are being tested in trial NCT05312437?

The interventions under investigation include: Interruptive Alert, CDS (OTHER), Passive Prompt, CDS (OTHER).

Who is sponsoring clinical trial NCT05312437?

This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05312437's enrollment target sits among peer trials

596 174th of 2000 higher than 1,827 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02138734 · 596 participants · Phase 1

    A Study of Intravesical BCG in Combination With ALT-803 in Patients With Non-Muscle Invasive Bladder Cancer

  • NCT06797245 · 596 participants · NA

    APPROVE Trial: Evaluating a Prescription Digital Therapeutic for Treatment of OAB in Women

  • NCT07100080 · 596 participants · Phase 2

    Study of Izalontamab Brengitecan (BMS-986507) Versus Platinum-Pemetrexed for EGFR-mutated Non-small Cell Lung Cancer After Failure of EGFR TKI Therapy (IZABRIGHT-Lung01)

  • NCT05723198 · 595 participants · Phase 3

    A Study of Baricitinib (LY3009104) in Children From 6 Years to Less Than 18 Years of Age With Alopecia Areata

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05312437, the US trial registry maintained by the National Library of Medicine. NCT05312437 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.