Postpartum depression
Related entities
Findings (50)
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementMothers who received PREPP reported significantly fewer bouts of infant fussing and crying at 6 weeks postpartum than mothers in the ETAU group.
Effect: improvement; F (1, 28) = 5.68
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54
None
improvementWomen who received PREPP decreased significantly in clinician-rated depressive symptoms (HRSD) between pre-randomization and 6 weeks postpartum, while ETAU women showed no significant change.
Effect: improvement; B = −6.54