Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04752618

Safe Mothers, Safe Children Initiative

Led by New York University · Updated on 2026-05-07

160

Participants Needed

1

Research Sites

312 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to assess the efficacy of the combined interventions, Skills Training in Affective and Interpersonal Regulation (STAIR) and Parent-Child Interaction Therapy (PCIT) or P-STAIR, for treating maternal PTSD and reducing maltreatment recidivism.

CONDITIONS

Official Title

Safe Mothers, Safe Children Initiative

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Mothers receiving preventive family preservation services at the time of consent
  • Meet a PTSD severity score of 28 or higher or probable DSM-5 PTSD diagnosis
  • Have a child aged 1 to 10 years
  • Be the legal guardian with physical and legal custody of the child
  • Be able to read, write, and speak English or Spanish
Not Eligible

You will not qualify if you...

  • Suicidal ideation in the past month or suicide attempt in the past year
  • Severe substance or alcohol use disorder without at least 3 months remission
  • Current psychosis symptoms in the past month
  • Disabilities affecting communication, such as deafness
  • Child with developmental conditions impacting cognitive or physical functioning
  • Child with current symptoms or diagnosis of psychosis in the past 3 months
  • Current or recent intimate partner or family violence, unless the relationship ended at least 90 days ago with no intention to restart or no violence occurred in the past year

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

McSilver Institute for Poverty Policy and Research

New York, New York, United States, 10003

Actively Recruiting

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Research Team

E

Erin A Montion, MA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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