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Preventing Postpartum Depression in African American Home Visiting Clients

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Johns Hopkins University

Status and phase

Completed
Phase 2

Conditions

Depression

Treatments

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

Study type

Interventional

Funder types

Other

Identifiers

NCT01175603
ICTR 2009 (Other Identifier)
JHMI ICTR 2009

Details and patient eligibility

About

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.

Full description

This study will conduct a randomized controlled trial (RCT) with women from four Baltimore City home visiting programs. We will screen 200 women who are pregnant or have a child < 6 months for study inclusion; 91 women at elevated risk for developing postpartum depression (PPD) will be randomized to an intervention (MB Course) or usual home visiting control group. Women in the intervention group will receive the 6-week MB Course delivered in a group setting by the Study Clinician with reinforcing messages provided by home visitors during 1-on-1 home visits, while women in the attention control will receive usual home visiting services and information on postpartum depression. Primary outcomes include depressive symptoms and depressive episodes.

Enrollment

82 patients

Sex

Female

Ages

14 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • pregnant or has child < 6 months of age
  • enrolled in home visiting program
  • exhibiting elevated depressive symptoms and/or personal history of clinical depression

Exclusion criteria

  • no current clinical depression at time of enrollment

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

82 participants in 2 patient groups

Cognitive behavioral intervention
Experimental group
Description:
Women in the intervention condition will receive 6 two-hour intervention sessions delivered weekly in a group format by the Study Clinician. Each session contains didactic instruction on core content, as well as activities and group discussion. One of the strengths of embedding the MB Course within home visiting is our ability to have home visitors reinforce the material presented by the Study Clinician. The 6-week curriculum is divided into three modules: (a) pleasant activities, (b) thoughts, and (c) relationships with others. Each module has two sessions. These sessions map onto core cognitive-behavioral concepts.
Treatment:
Behavioral: Mothers and Babies Course (Adapted for Baltimore Home Visiting Programs)
Usual home visiting
No Intervention group
Description:
Women in the control group will receive usual home visiting services and information on postpartum depression.

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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