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N/A N=42 Randomized Treatment

Mommy-Baby Treatment for Perinatal Depression

Depressive Disorder, Major · Postpartum Depression

Enrolled (actual)
42
Serious AEs
0.0%
Results posted
Jan 2022
Primary outcome: Primary: Change in Edinburgh Depression Scale From Baseline — 17.81; 17.9; 12.04; 11.41 units on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Dyadic Interpersonal Psychotherapy (Behavioral); Enhanced Treatment as Usual (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
Female
Sponsor
Washington University School of Medicine
Primary completion
Jan 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Edinburgh Depression Scale From Baseline
17.81; 17.9; 12.04; 11.41; 11.0; 10.3

Summary

Perinatal depression is a major public health problem, affecting 15% of women during pregnancy through the postpartum period, with adverse consequences for the mother, the fetus, the infant, and the family. Despite increasing evidence of the importance of this critical risk interval, little research has investigated the effects of depression treatment during pregnancy on infant outcomes. The purpose of this study is to test the feasibility, acceptability, and effectiveness of a new intervention, Interpersonal psychotherapy for the mother-infant dyad (IPT-Dyad). This intervention begins during pregnancy and continues with the mother and infant until one year postpartum. The investigators hypothesize that IPT-Dyad will be better than treatment as usual in reducing depressive symptoms, improving psychosocial functioning,increasing parenting self-efficacy, improving infant emotional development, and enhancing mother-infant relationship quality.

Eligibility Criteria

Inclusion Criteria

  • Pregnant women
  • 18 years and older
  • between 12 and 30 weeks gestation
  • Score greater than or equal to 13 on Edinburgh Depression Scale
  • Structured Clinical Interview (SCID-IV) diagnosis of Major Depressive Disorder, dysthymia, or Depressive Disorder, Not otherwise Specified
  • English Speaking

Exclusion Criteria

  • Substance abuse or dependence in past 3 months
  • Active suicidal or homicidal ideation
  • Bipolar disorder, psychotic disorder
  • unstable medical condition or other medical/obstetrical complication
  • Evidence of severe intimate partner violence
  • Ongoing psychosocial or pharmacotherapy for depression
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01744041). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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