Ignite Creation Date:
2024-07-17 @ 10:43 AM
Last Modification Date:
2024-10-26 @ 3:34 PM
Study NCT ID:
NCT06499740
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-07-15
First Post:
2024-07-05
Brief Title:
Adapting a Brief Suicide Intervention for Pediatric Primary Care Enhancing Uptake and Impact
Sponsor:
University of Washington
Organization:
University of Washington
Study Overview
Official Title:
Adapting a Brief Suicide Intervention for Pediatric Primary Care Enhancing Uptake and Impact
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Suicide is a leading cause of death among adolescents in the United States and improving access to high quality just-in-time suicide interventions to reduce risk has important public health implications Integrating such interventions into routinely accessed settings such as pediatric primary care holds promise however many clinicians in these settings fail to adequately screen or intervene in youth suicidal thoughts and behaviors representing a key barrier to reducing suicide The proposed study is a pre-post quasi-experimental pilot feasibility and preliminary efficacy trial of an adaptation of the SAFETY-Acute suicide prevention intervention implemented in 3 pediatric primary care clinics
Detailed Description:
This project aims to take an innovative user-centered design approach to adapt and optimize a brief evidence-based suicide intervention SAFETY-Acute SAFETY-A formerly known as Family Intervention for Suicide Prevention -aka FISP for use in primary care settings to support primary care management of adolescents with low to moderate risk suicidal thoughts and behaviors STB In this trial the investigators will conduct a pre-post quasi-experimental pilot feasibility and preliminary efficacy trial of an adapted STB model of care based of the SAFETY-Acute intervention compared to treatment as usual with 3 primary care clinics The trial will include 48 10-18-year-old patients with STB and their parentscaregivers 16 dyads per clinic The investigators will assess acceptability and feasibility of the STB model of care preliminary intervention impacts and need for further adaptation
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 1K23MH134229-01A1 | NIH | None | None |