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Reducing Fetal Exposure to Maternal Depression to Improve Infant Risk Mechanisms

Not Applicable
Completed
Conditions
Depression
Interventions
Behavioral: Interpersonal Therapy
Behavioral: Enhanced usual care
Registration Number
NCT03011801
Lead Sponsor
University of Illinois at Urbana-Champaign
Brief Summary

This study evaluates Interpersonal Therapy (IPT) in the treatment of depression among pregnant women with elevated depressive symptoms. Half of the women will be randomized to receive IPT, and the other half will get Treat As Usual, provided via behavioral health in the hospital.

Detailed Description

Exposure to maternal depressive symptoms is one of the most well established risk factors for the development of later child psychopathology. Accumulating evidence from naturalistic observational studies documents that fetal exposure to maternal depressive symptoms is associated with risk for later child mental health problems. Maternal depression is one of the most common prenatal complications with approximately 40% of women experiencing elevated levels of depressive symptoms. The majority of past research has been correlational, so potential causal conclusions have been limited. This project will break new ground by testing the hypothesis that manipulating maternal depressive symptoms will benefit infant outcomes. In this project, maternal depressive symptoms will be reduced using brief interpersonal therapy (IPT), a well-established and efficacious treatment, and testing whether this reduction leads to an improvement in the development of infant mechanisms associated with risk for later psychopathology. The investigators propose to assess 300 pregnant women who report elevated levels of depressive symptoms and their infants. Prior to the intervention, maternal measures of depressive symptoms will be collected. Then half of the women will be randomized to receive IPT and the other half will receive enhanced usual care (TAU). After completion of the intervention, maternal measures will be collected longitudinally through 14 months postpartum. Infants will be evaluated at birth and two other times. Infants will be assessed across four units of analysis (brain structure and function, physiology, behavior, and maternal-report).

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
234
Inclusion Criteria
  • Adult women (over 18 years of age)
  • A singleton intrauterine pregnancy
  • English speaking
  • Elevated depressive symptoms based on screening with the Edinburgh Postnatal Depression Scale (EPDS) with score > 9
Exclusion Criteria
  • Bipolar disorder and psychosis based on the Structured Clinical Interview for DSM-IV Axis I Disorders (SCID-NP)
  • Current psychotropic medication use or current CBT/IPT usage
  • An HPA axis or an endocrine disorder
  • Maternal substance use [assessed using maternal report and urine toxicology
  • Corticosteroid medication use during this pregnancy
  • Invitto fertilization
  • Presence of cervical or uterine abnormalities

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Behavioral: Interpersonal TherapyInterpersonal TherapyIndividual psychotherapy that includes an initial engagement session and a total of 8 sessions. IPT focuses on psychoeducation and interpersonal skill building to decrease interpersonal conflict and increase interpersonal support and competence.
Enhanced Usual CareEnhanced usual careMaternity support services (MSS) is the usual standard of care for pregnant women. A multi-disciplinary team of obstetric care providers routinely screen women for possible depression diagnosis. If a woman screens positive, she is seen by a behavioral health specialist (BHS) for further assessment and to initiate treatment, if necessary. The goals of MSS include offering services to promote healthy pregnancies and positive birth and parenting outcomes, including integrating mental health and prenatal care. Women with elevated depressive symptoms are seen by BHS throughout the pregnancy and postpartum period and then bridged to mental health treatment. BHS provides eclectic-based care but does not provide IPT.
Primary Outcome Measures
NameTimeMethod
Symptom Checklist 20 (SCL20)12 months post intervention

Self reported Depression Scores. higher scores=more depression

Presence of a Major Depressive Episode on SCID interview12 months post pregnancy

Presence of a depression diagnosis as measured by a semi-structured diagnostic evaluation

Secondary Outcome Measures
NameTimeMethod
Edinburgh Postnatal Depression Scale (EPDS)12 months post intervention

Self reported Depression Scores. higher scores=more depression

Work and Social Adjustment Scale (WSAS)12 month post intervention

general maternal functioning

Trial Locations

Locations (2)

University of Denver

🇺🇸

Denver, Colorado, United States

University of Illinois

🇺🇸

Urbana, Illinois, United States

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