RECRUITING

Safe Mothers, Safe Children Initiative

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Treating Maternal PTSD to Enhance and Reduce Maltreatment Recidivism: Safe Mothers, Safe Children

Quick Facts

Study Start:2021-05-01
Study Completion:2025-09-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04752618

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Receiving preventive services
  2. * Meeting a severity score of 28 or higher OR probable DSM-5 diagnostic criteria for PTSD (PDS-5)
  3. * Having 1-8-year-old child
  4. * Being the legal guardian for the child with physical and legal custody
  5. * Being able to read, write, and speak English or Spanish
  1. * Having suicidal ideation present in the past month prior to pre-assessment or reports of a suicide attempt in the past year (SCID-5)
  2. * Meeting a diagnosis of severe substance or alcohol use disorder (≥ 6 symptoms on SCID) AND not in early remission (≥3 months without meeting any substance or alcohol use disorder criteria (except craving)
  3. * Having current or active symptoms of psychosis in the past month
  4. * Having a disability affecting communication, such as deafness
  5. * Having an index child with a developmental condition that impedes cognitive and/or physical functioning, e.g. autism
  6. * Having an index child with current symptoms or diagnosis of psychosis as defined by the DSM-5 in the past 3 months
  7. * Experiencing current or history of intimate partner violence (IPV) or family violence:

Contacts and Locations

Study Contact

Hanaan Osman
CONTACT
212-998-4296
ho2233@nyu.edu

Principal Investigator

Michael A Lindsey
PRINCIPAL_INVESTIGATOR
New York University

Study Locations (Sites)

McSilver Institute for Poverty Policy and Research
New York, New York, 10003
United States

Collaborators and Investigators

Sponsor: New York University

  • Michael A Lindsey, PRINCIPAL_INVESTIGATOR, New York University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-05-01
Study Completion Date2025-09-30

Study Record Updates

Study Start Date2021-05-01
Study Completion Date2025-09-30

Terms related to this study

Additional Relevant MeSH Terms

  • PTSD
  • Depression
  • Child Maltreatment