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Table 1 Randomized trials examining the effectiveness of ROSE in preventing PPD

From: Protocol for the ROSE sustainment (ROSES) study, a sequential multiple assignment randomized trial to determine the minimum necessary intervention to maintain a postpartum depression prevention program in prenatal clinics serving low-income women

Population

Sample size

% with PPD: ROSE

% with PPD: usual care

Time post-partum

Pregnant women on public assistance [29]

37

0%*

33%

12 weeks

Women on public assistance at risk for PPD [27]a

99

4%*

20%

3 months

Pregnant women on public assistance at PPD risk [28]

205

16%*

31%

6 months

Pregnant adolescents [39]

106

12.5%

25%b

6 months

African-American women at risk for PPD [40]a

36

Depressive symptoms decreased over time

No change in depressive symptoms

3 months

  1. *p < .05 between conditions
  2. aPer Cooper Survey Questionnaire [76]
  3. bDose-matched control