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Trial record 1 of 264 for:    Postpartum Depression AND Postpartum Depression | "Depression" AND "Depression"
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PREPP: Preventing Postpartum Depression (PREPP)

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ClinicalTrials.gov Identifier: NCT03283254
Recruitment Status : Recruiting
First Posted : September 14, 2017
Last Update Posted : January 29, 2018
Sponsor:
Information provided by (Responsible Party):
New York State Psychiatric Institute

Brief Summary:
The primary aim of this study is to determine if a behavioral intervention targeting maternal caregiving of young infants can increase infant sleep and reduce fuss/cry behavior, and thereby (1) reduce the incidence and/or severity of postpartum maternal depression and (2) improve the quality of the mother-infant interaction and subsequent child development. Specifically, the study team will investigate: (1) the effectiveness of the intervention compared to usual care; (2) if the effects of the intervention can be detected in the assessments of the quality of mother-infant interaction; (3) if there are prenatal and/or postnatal biomarkers that can help identify infants whose behavior is more likely to play a role in their mothers' depression; (4) if these markers differentiate which infants will be most responsive to the intervention(s); and (5), if assessments of brain function at birth and at 4-6 weeks of age provide biological nodal points for identifying the effects of the intervention on infant brain development. Participants will be recruited during their 2nd trimester, and will be randomly separated into one of two groups: a group that receives coaching in parenting techniques (4 in-person coaching sessions and 1 phone session) or one that receives treatment as usual.

Condition or disease Intervention/treatment Phase
Postpartum Depression Behavioral: Practical Resources for Effective Postpartum Parenting Behavioral: Enhanced Treatment As Usual Not Applicable

Detailed Description:

Of the nearly 4 million mothers delivering live births each year in the United States, approximately 560,000 — or 14% — will develop major or minor depression within the first four months postpartum, when the rate peaks. This number dwarfs prevalence rates for gestational diabetes (2-5%) and is comparable to preterm birth (11.4%). Postpartum depression (PPD) has substantial consequences: poorer maternal quality of life, significant emotional suffering, and suicide risk. PPD predicts diminished mother-infant bonding, and poor outcomes in social-emotional and, in some groups, cognitive development. PPD is undertreated in part because women are reluctant to seek treatment due to the stigma associated with mental health care, logistical barriers to at-tending added health care appointments, and disinclination to take medications while breastfeeding. Of preventive interventions, few embed services in obstetrical care or leverage the unique mother-infant dyadic orientation of the childbearing period. The investigators developed a novel intervention based on the conceptualization of maternal depression as a potential disorder of the mother-infant dyad, and one that can be approached through psychological and behavioral changes in the mother — commencing before birth — that affect her and the child. PREPP (Practical Resources for Effective Postpartum Parenting) enrolls distressed pregnant women at risk for PPD, spans late pregnancy to the 6 week postpartum check up, comprises four in-person 'coaching' sessions adjunctive to obstetrical (OB) prenatal and postnatal appointments, one phone session, and imparts (a) mindfulness and self-reflection skills, (b) parenting skills, and (c) psycho-education.

The primary aim of this study is to determine if a behavioral intervention targeting maternal caregiving of young infants can increase infant sleep and reduce fuss/cry behavior, and thereby (1) reduce the incidence and/or severity of postpartum maternal depression and (2) improve the quality of the mother-infant interaction and subsequent child development.


Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 300 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Two groups: One receives PREPP prevention intervention and the other group receives Enhanced Treatment as Usual (psychoeducation about Postpartum Depression, referral and monitoring)
Masking: Single (Outcomes Assessor)
Masking Description: The person administering the outcome measures is blind to participant group.
Primary Purpose: Prevention
Official Title: Preventing Postpartum Depression: A Dyadic Approach Adjunctive to Obstetric Care
Actual Study Start Date : October 17, 2017
Estimated Primary Completion Date : July 20, 2022
Estimated Study Completion Date : August 10, 2022

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Practical Resources for Effective Postpartum (PREPP)
A psychotherapeutic preventive intervention that involves psychoeducation and cognitive behavioral techniques.
Behavioral: Practical Resources for Effective Postpartum Parenting
A preventive psychotherapy intervention for Postpartum Depression
Other Name: PREPP

Active Comparator: Enhanced Treatment as Usual
Psychoeducation about Postpartum Depression, referral to treatment in the community and monitoring
Behavioral: Enhanced Treatment As Usual
Psychoeducation about Postpartum Depression, referral to treatment in the community, clinical monitoring
Other Name: ETAU




Primary Outcome Measures :
  1. Postpartum Depression Symptoms [ Time Frame: 6-16 weeks postpartum ]
    Postpartum Depression Symptoms measured by Edinburgh Postnatal Depression Scale


Secondary Outcome Measures :
  1. Improved Sleep [ Time Frame: 3rd trimester of pregnancy - 16 weeks postpartum ]
    Improved self-report of sleep quality on Pittsburgh Sleep Quality Index and improved sleep shown on actigraphy monitor

  2. Infant Behavior [ Time Frame: 6 & 16 weeks postpartum ]
    Cry behavior and sleep behavior measured by The Baby Day Diary

  3. Greater infant left frontal EEG power reflecting sleep spindle activity [ Time Frame: Newborn-6 weeks postpartum ]
    More positive perceptions and objective assessments of maternal postpartum sleep efficiency will be mediated by greater infant left frontal EEG power reflecting sleep spindle activity and associated longer average durations of infant nocturnal sleep per maternal report and actigraphy.



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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. Healthy pregnant women between 18-45 years old (based on self report)
  2. A score of ≥21 on the Predictive Index of Postnatal Depression (PIPD), indicating risk for developing postpartum depression
  3. A healthy, singleton pregnancy (based on self report)
  4. English speaking (based on self report)
  5. Receiving standard prenatal care (based on self report)

Exclusion Criteria:

  1. Multi-fetal pregnancy (based on self-report)
  2. Smoking, illicit drug use, or alcohol use during pregnancy (based on self-report)
  3. Acute medical illness or significant pregnancy complication (based on self-report)
  4. Currently in weekly, individual psychotherapy, including psychopharmacology (based on self report)
  5. Psychotic d/o; Bipolar I; Major Depressive d/o (based on M.I.N.I.)

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03283254


Contacts
Contact: Elizabeth Werner, Ph.D. 6463191008 ew150@cumc.columbia.edu
Contact: Catherine Monk, Ph.D. 917-543-6031 cem31@cumc.columbia.edu

Locations
United States, New York
Elizabeth Werner Recruiting
New York, New York, United States, 10032
Contact: Elizabeth Werner, Ph.D.    646-774-8945    ew150@cumc.columbia.edu   
Contact: Catherine Monk, Ph.D.    646-774-8941    cem31@cumc.columbia.edu   
Principal Investigator: Catherine Monk, PhD         
Sponsors and Collaborators
New York State Psychiatric Institute
Investigators
Principal Investigator: Catherine Monk, Ph.D. Columbia University
Study Director: Elizabeth Werner, Ph.D. Columbia University

Responsible Party: New York State Psychiatric Institute
ClinicalTrials.gov Identifier: NCT03283254     History of Changes
Other Study ID Numbers: 7428
First Posted: September 14, 2017    Key Record Dates
Last Update Posted: January 29, 2018
Last Verified: January 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided
Plan Description: De-identified data may be made available to other researchers.

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by New York State Psychiatric Institute:
Postpartum Depression Treatment

Additional relevant MeSH terms:
Depression
Depressive Disorder
Depression, Postpartum
Behavioral Symptoms
Mood Disorders
Mental Disorders
Puerperal Disorders
Pregnancy Complications