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NCT06164106 · ClinicalTrials.gov registry record · NA
Feasibility Trial of a Single Session of Crisis Response Planning for Youth at High Risk for Suicide
A NA study of Suicide Prevention, sponsored by Ohio State University.
- Completed
- Registry status
- NA
- Development phase
- 57
- Enrollment target
- 1
- Study location
NCT06164106 is a NA study of Suicide Prevention that has completed, run by Ohio State University. The registered enrollment target is 57 participants, below the 950-participant average among 21 other Suicide Prevention trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06164106, a NA study of Suicide Prevention, has completed, sponsored by Ohio State University.
- COMPLETED
- Registry status
- NA
- Development phase
- 57 participants
- Enrollment target
- 1
- Study location
Study Summary
The current study is a clinical trial, meaning a research study in which human subjects are prospectively assigned to one or more interventions to evaluate the effects of those interventions on health-related behavioral outcomes. Specifically, male and female adolescents with current suicidal intent will be randomly assigned to receive either a 1-hour session of virtual crisis response planning (CRP), a 1-hour session of in-person CRP, or a 1-hour session of standard crisis risk management (treatment as usual). The feasibility and acceptability of the virtual CRP, compared to in-person CRP, will be assessed 14 days post-treatment. Additional assessments of changes in mood, behavior, and suicidality will be collected daily for 14 days post-treatment via ecological momentary assessments. The investigators hypothesize the following: 1) Virtual CRP will be rated as more feasible and acceptable compared to traditional CRP and treatment as usual interventions; 2) Both versions of CRP will be associated with changes in frequency and severity of suicidal ideation and behavior compared to treatment as usual; 3) Virtual CRP will be equally as effective as traditional CRP at reducing suicide risk, suggesting that virtual CRP is a promising scalable intervention adaptation.
Conditions Studied
Interventions
- BEHAVIORAL Crisis Risk Counseling
- BEHAVIORAL Virtual Crisis Response Planning
- BEHAVIORAL In-Person Crisis Response Planning
Study Locations (1)
Ohio
- Ohio State University - Columbus
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 57 participants |
| Start Date | 2023-11-01 |
| Est. Completion | 2025-01-22 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06164106
The ClinicalTrials.gov registry entry for NCT06164106 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 57 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 950-participant average among 21 other Suicide Prevention trials with a reported enrollment target (94% lower). The listed sponsor is Ohio State University, which has 552 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Suicide Prevention appearing as the primary indexed condition, and to 3 interventions - of which Crisis Risk Counseling is the first listed.
NCT06164106 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.
Frequently Asked Questions
What is clinical trial NCT06164106 about?
NCT06164106 is a clinical study titled "Feasibility Trial of a Single Session of Crisis Response Planning for Youth at High Risk for Suicide". The current study is a clinical trial, meaning a research study in which human subjects are prospectively assigned to one or more interventions to evaluate the effects of those interventions on health-related behavioral outcomes. Specifically, male and female adolescents with current suicidal intent...
What is the current status of trial NCT06164106?
This trial is currently completed. It is a NA study. The enrollment target is 57 participants. The study started on 2023-11-01. Estimated completion is 2025-01-22.
What conditions does trial NCT06164106 study?
This clinical trial studies the following conditions: Suicide Prevention.
What interventions are being tested in trial NCT06164106?
The interventions under investigation include: Crisis Risk Counseling (BEHAVIORAL), Virtual Crisis Response Planning (BEHAVIORAL), In-Person Crisis Response Planning (BEHAVIORAL).
Who is sponsoring clinical trial NCT06164106?
This trial is sponsored by Ohio State University, which has 552 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06164106 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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