Managing PPD at Gouverneur

NYU Langone Health

Status: Withdrawn

Conditions: Post-Partum Depression

Treatments: Behavioral: STRONG

Study type: Interventional

Funder types: Other

Identifiers

NCT02738021

15-00416

Details and patient eligibility

About

A Stepped Care pathway for managing postpartum depression (PPD) in pediatric primary care settings will be used to (1) understand context for implementation feasibility (2) evaluate benefits for mother and child.

The proposed pilot project will be conducted as part of a quality improvement effort in the Department of Pediatrics at Gouverneur Health Services to improve management of postpartum depression during pediatric primary care visits. This project will test the feasibility of a stepped care approach to identifying and managing depression among mothers of infants (0-6 months). This study will provide preliminary data on the feasibility of the care management protocol, implementation and fidelity measures, and training/consultation methods within a real world pediatric care practice. These data will inform and support the preparation of a large-scale NIH grant.

Specific research questions include:

1. To pilot the feasibility of using a Stepped Care Approach to identify and mange maternal depression within primary care pediatric care visits, with a focus on mothers of infants 0-6 months.

   1. Train non specialty MH providers to systematically identify maternal depression.
   2. Assess how effective integration of maternal depression intervention is as part of well baby visits.

2. To o examine the impact of STRONG, a brief 3-session IPT-based preventive intervention, on maternal and child health outcomes (e.g., maternal depression symptoms, child receipt of acute care services). Secondary outcomes include maternal social support and parenting practices.

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for Subjects

• PHQ-9 scores in the 10-19 range
• Women with infants 6 months and younger at time of screening

Inclusion Criteria for Providers

Exclusion Criteria:

• Active substance use
• Current treatment for depression
• Current/past history of schizophrenia, bipolar or other psychotic disorder;
• Suicidal/Homicidal risks;
• Women with difficulties speaking or understanding English;
• Women under the age of 18.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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0 participants in 1 patient group

STRONG

Experimental group

Description:

A brief 3-session IPT-based preventive intervention, on maternal and child health outcomes.

Treatment:

Behavioral: STRONG