Preventing Postpartum Depression in Prenatal Care

NYU Langone Health

Overview

This is randomized control trial of a brief intervention called Bellevue ROSE (Reach Out Stay Strong Essentials). Bellevue ROSE is a manualized and highly structured interpersonal intervention that provides women with psycho-education about maternal depression and strategies for strengthening social support and connectedness. Investigators use motivational interviewing strategies to improve treatment compliance and resource acquisition

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

DOUBLE

Conditions

Post-partum Depression

Interventions

Bellevue ROSE InterventionBEHAVIORAL

Psycho-education session and usual, Standard of care ControlBEHAVIORAL

Psycho Education and usual, standard of care

One Psycho-education session and usual, standard of care ControlBEHAVIORAL

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 45 Years

Medical Language ↔ Plain English

Inclusion Criteria: * English speaking * Women who score between 5-19 on the PHQ-9 and \>23 on the ANRQ Exclusion Criteria: * Women who score \<5 or \>19 on the PHQ-9 * Women who are currently suicidal, active substance users, currently experiencing domestic violence, or have a current or past history of bipolar or psychotic disorder diagnosis. * Women who are currently in treatment for psychotherapy. * Unable to speak and/or understand English proficiently * Unable to provide informed consent

Locations (1)

New York University School of Medicine

New York, New York, United States

Outcomes

Primary Outcomes

Depression severity measured by Patient Health Questionnaire (PHQ-9)

Time frame: 6 Months

Measure of psycho social risk assessment according to Adapted antenatal Risk Questionnaire (ANRQ)

Time frame: Screening

Measure of perceived social support measured by Multidimensional Scale of Perceived Social Support (MSPSS)

Time frame: 6 Months

Measure of stress using Perceived Stress Index (PSS)

Time frame: 6 Months

Parenting Practices and treatment assessed by Parenting Practices and Treatment Questionnaire

Time frame: 6 Months

Data from ClinicalTrials.gov

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