ExploreConditionEducation about postpartum depression
Condition

Education about postpartum depression

Also known as: Education about postpartum depression Education about postpartum depression (procedure) postpartum depression; anxiety PPD
3 findings 1 paper 4 related entities View in graph →

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interventions
outcomes
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Findings (27)

None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84
None
improvement

Women who received PREPP decreased significantly in clinician-rated anxiety symptoms (HAM-A) between pre-randomization and 6 weeks postpartum, with effects persisting to 16 weeks, while ETAU women sho

Effect: improvement; B = −7.84

Size: B = −7.84

Papers (1)