RECRUITING

PTSD Screening in Pregnant Black Women

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

This study will compare the effectiveness of two active screening interventions in improving post-traumatic stress disorder (PTSD) symptoms, maternal perinatal care utilization, satisfaction utilization of mental healthcare services, and maternal health and birth-related outcomes for Black pregnant women.

Official Title

Comparing Two Screening Approaches for PTSD to Improve Health Outcomes in Pregnant Black Women

Quick Facts

Study Start:2025-02-20
Study Completion:2029-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06522022

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:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 18+ years old,
  2. * Ability to provide informed consent,
  3. * English-speaking,
  4. * Willingness to participate in the study,
  5. * Self-identification as Black or African American,
  6. * Pregnant and in the first trimester attending initial prenatal care visit,
  7. * Endorsement of at least one traumatic event in their lifetime.
  1. * Active suicidality

Contacts and Locations

Study Contact

Abigail Powers Lott, PhD, ABPP
CONTACT
404-712-0159
abigail.lott@emoryhealthcare.org

Principal Investigator

Abigail Lott, PhD, ABPP
PRINCIPAL_INVESTIGATOR
Emory University
Briana Woods-Jaeger, PhD
PRINCIPAL_INVESTIGATOR
Emory University

Study Locations (Sites)

Grady Health System
Atlanta, Georgia, 30303
United States
Truman Medical Center (TMC) system
Kansas City, Missouri, 64108
United States

Collaborators and Investigators

Sponsor: Emory University

  • Abigail Lott, PhD, ABPP, PRINCIPAL_INVESTIGATOR, Emory University
  • Briana Woods-Jaeger, PhD, PRINCIPAL_INVESTIGATOR, Emory 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 Date2025-02-20
Study Completion Date2029-03

Study Record Updates

Study Start Date2025-02-20
Study Completion Date2029-03

Terms related to this study

Keywords Provided by Researchers

  • Pregnancy
  • Black Women
  • Screening for Maternal PTSD
  • Obstetric Care
  • African-American Women

Additional Relevant MeSH Terms

  • Pregnancy Early
  • PTSD