RECRUITING

ROSE in Sunset Park

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 learn more about pregnant women's' experience with Reach Out, Stay Strong, Essentials for mothers of newborns (ROSE) and to evaluate the effectiveness of the ROSE program in preventing and reducing post-partum depressive symptoms, decreasing stress, and increasing social support among pregnant women.

Official Title

Reach Out, Stay Strong, Essentials for Mothers of Newborns (ROSE), a Study of a Postpartum Depression Prevention Intervention Among Pregnant Women in a Women's Health Clinic

Quick Facts

Study Start:2021-03-21
Study Completion:2026-08-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04940585

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 to 100 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Receive prenatal care at the Sunset Park Family Health Center for Women's Health and Pediatrics (SPWHP)
  2. * Female
  3. * At least 18 years of age
  4. * Speaks and understands English or Spanish (depending on the language of the next group)
  5. * Is pregnant
  6. * Is in the second trimester of her pregnancy
  7. * Capable of providing informed consent.
  8. * Scores between 4 and 12 on Edinburgh Postnatal Depression Scale or records 2 or more ACEs on adapted ACEs questionnaire
  1. * Not receiving prenatal care at the Sunset Park Family Health Center for Women's Health and Pediatrics (SPWHP)
  2. * Not female
  3. * Under18 years of age
  4. * Does not speak and understand English or Spanish
  5. * Is not pregnant
  6. * Is not in the second trimester of her pregnancy
  7. * Is not capable of providing informed consent.
  8. * Scoring \< 4or \>12 on Edinburgh Postnatal Depression Scale and scores 1 or less on adapted ACEs questionnaire.
  9. * Positive score to #10 on the Edinburgh Postnatal Depression Scale

Contacts and Locations

Study Contact

Juliana Zeller
CONTACT
646-951-6568
Juliana.Zeller@nyulangone.org

Principal Investigator

Bonnie Kerker, PhD
PRINCIPAL_INVESTIGATOR
NYU Langone Health

Study Locations (Sites)

NYU Langone Health
New York, New York, 10016
United States

Collaborators and Investigators

Sponsor: NYU Langone Health

  • Bonnie Kerker, PhD, PRINCIPAL_INVESTIGATOR, NYU Langone Health

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 Date2021-03-21
Study Completion Date2026-08-31

Study Record Updates

Study Start Date2021-03-21
Study Completion Date2026-08-31

Terms related to this study

Additional Relevant MeSH Terms

  • Post Partum Depression