Ignite Creation Date:
2024-05-06 @ 8:16 PM
Last Modification Date:
2024-10-26 @ 3:24 PM
Study NCT ID:
NCT06318663
Status:
RECRUITING
Last Update Posted:
2024-03-20
First Post:
2024-03-11
Brief Title:
Survivor Mom Companion Comparison Study
Sponsor:
State University of New York at Buffalo
Organization:
State University of New York at Buffalo
Study Overview
Official Title:
Survivor Moms Companion A Perinatal PTSD Program
Status:
RECRUITING
Status Verified Date:
2024-03
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:
SMC
Brief Summary:
The overall goal of the SMC is to help reduce posttraumatic stress symptomology for pregnant persons with a history of trauma
Detailed Description:
The study is a pilot randomized waitlist-controlled trial that examines the preliminary efficacy of the SMC for reducing PTSD symptomology as compared to a waitlist control group Also it aims to assess the feasibility and acceptability of the SMC It examines how changes in the theorized mechanisms emotion regulation interpersonal sensitivity mediate the relationship between the intervention and PTSD symptomology
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