ConditionPost Partum Depression
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-100
SponsorNYU Langone Health
About this trial
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.
Eligibility criteria
Qualifiers
Receive prenatal care at the Sunset Park Family Health Center for Women's Health and Pediatrics (SPWHP)
Female
At least 18 years of age
Speaks and understands English or Spanish (depending on the language of the next group)
Disqualifiers
Not receiving prenatal care at the Sunset Park Family Health Center for Women's Health and Pediatrics (SPWHP)
Not female
Under18 years of age
Does not speak and understand English or Spanish
Trial design
Treatments tested in this trial
- ROSE Program
Treatment groups
308 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov