Preventing Postpartum Depression in African American Home Visiting Clients

NCT01175603 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 82

Last updated 2016-04-07

No results posted yet for this study

Summary

The goal of this study is to determine whether a 6 week intervention is effective in preventing the worsening of depressive symptoms and development of clinical depression in low-income African American pregnant and recently delivered women who are enrolled in home visiting programs.

Conditions

Interventions

BEHAVIORAL

Mothers and Babies Course (Adapted for Baltimore Home Visiting Programs)

6 weekly 2-hour cognitive-behavioral intervention sessions held in group format

Sponsors & Collaborators

Principal Investigators

  • Shiv D Tandon, PhD · Johns Hopkins University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
14 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-10-31
Primary Completion
2010-10-31
Completion
2010-10-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01175603 on ClinicalTrials.gov