Viewing Study NCT05490004



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Last Modification Date: 2024-10-26 @ 2:38 PM
Study NCT ID: NCT05490004
Status: RECRUITING
Last Update Posted: 2023-04-04
First Post: 2022-07-28

Brief Title: RISE With Veteran Service Providers
Sponsor: McMaster University
Organization: McMaster University

Study Overview

Official Title: Evaluating an Educational Intervention for Improving Provider Recognition and Response to Intimate Partner Violence IPV Experienced by Veterans and Their Families - A Mixed Method Pilot Randomized Trial
Status: RECRUITING
Status Verified Date: 2023-04
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: RISE Vet
Brief Summary: Veterans and their families are more likely to experience forms of family violence like intimate-partner violence and child maltreatment Evidence suggests that healthcare and social service providers HSSPs need more training to effectively and confidently recognize and respond to these situations The Violence Evidence Guidance Action VEGA Educational Intervention is a novel education intervention aimed at improving providers preparation for these clinical encounters The goal of this project is to determine the acceptability and feasibility of a future randomized-controlled trial comparing two approaches facilitator-led VEGA or self-directed VEGA to administering the VEGA training to understand whetherhow these approaches can support HSSPs continued care of veterans and their families The investigators aim to generate initial estimates of the effectiveness of both approaches in improving HSSPs knowledge and skills to effectively recognize and respond to intimate-partner violence and related forms of family violence including child maltreatment As well the investigators aim to contribute to the knowledge base regarding optimal educational approaches for HSSP education in family violence

The investigators hypothesize that there will be significant increases in preparedness knowledge and skills and self-efficacy to recognize and respond to both CM and IPV in both the experimental and AC arms from Time 1 baseline to Time 2 immediately after the intervention and Time 1 baseline to Time 3 3 month follow-up These improvements will be slightly attenuated in the experimental arm Qualitative data pertaining to perceived value and impact will corroborate the quantitative findings
Detailed Description: None

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