Social Circumstances, Parenting Techniques, and Infant Development

Postpartum Depression Clinical Trial

Official title:

Social Circumstances, Parenting Techniques, and Infant Development

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02121496
• Other study ID #: #6889
• Status: Completed
• Phase: N/A
• Start date: March 2014
• Est. completion date: December 2019

Study information

• Verified date: January 2020
• Source: New York State Psychiatric Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

1. Investigators aim to assess a novel behavioral intervention (currently approved in Protocol #6285) behavioral intervention that promotes maternally-mediated behavioral changes in young infants to reduce the risk of postpartum depression in a group of low income women. More specifically, investigators aim 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 in low socioeconomic status (SES) women, and (2) improve the quality of mother-infant interaction and subsequent child development. Investigators will study:

1. The feasibility of applying this protocol with a low SES population

2. The effectiveness of the intervention compared to usual care

3. If the effects of the intervention can be detected in assessments of the quality of mother-infant interaction and infant neurocognitive development

2. Investigators aim to determine whether this behavioral intervention can affect infant development as measured by neurodevelopmental assessments and cortisol reactivity at 4 months of age.

Description:

Developmental research consistently shows that postpartum depression has a negative impact on cognitive and emotional development during infancy and childhood. Low SES women face unique stressors and social challenges. Rates of postpartum depression are significantly higher in this group (23-33%) than in the general population (10-15%).

The purpose of this study is to understand how social circumstances, women's mood, and parenting techniques affect infant and child development. Specifically, investigators are interested in finding out whether a behavioral intervention, already being administered in IRB approved protocol #6285, targeting maternal caregiving of young infants can increase infant sleep and reduce fuss/cry behavior, thereby reducing the incidence and/or severity of maternal depression and anxiety symptoms, improving the quality of the mother-infant interaction, and improving infant developmental outcomes.

By collecting stress reports from women from low SES backgrounds during pregnancy and the postpartum period and by conducting follow-up observational assessments of the quality of mother-infant interaction, infant learning, infant cortisol reactivity, and infant neurocognitive development, investigators hope to identify whether this intervention can effectively meet these aims.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: December 2019
• Est. primary completion date: December 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

• Healthy pregnant women between 24 and 38 weeks gestation (based on self-report)

• Ages 18-45 (based on self-report) 3. English speaking (based on self-report)

• Salary indicated to be at New York City standardized "Struggling level" or lower - $47,700 annual for a family of 4 (based on self-report)

• Experiencing one or more of nine social adversity hardships (based on self report)

• Experiencing a healthy pregnancy, free from any significant medical complication (based on self-report)

• Receiving standard prenatal care (based on self-report)

Exclusion Criteria:

• Multi-fetal pregnancy (based on self-report)

• Smoking, illicit drug use, or alcohol use during pregnancy (based on self-report)

• Acute medical illness or significant pregnancy complication (based on self-report)

• Currently in weekly, individual psychotherapy - group therapy and psychiatric management ok (based on self-report)

• Psychotic d/o; Bipolar I; Major Depressive d/o (based on M.I.N.I.)

Related Conditions & MeSH terms

• Depression
• Depression, Postpartum
• Infant Development
• Postpartum Depression
• Rhythm; Sleep

Intervention

Behavioral:
• Resources for Postpartum Parenting
The intervention includes four-sessions that targets maternal caregiving of young infants to increase infant sleep and reduce fuss/cry behavior and thereby simultaneously consolidate women's enjoyment of and confidence in their maternal role, this, in turn, promotes a cycle of a mutually re- warding engagement in the mother-infant dyad — the antithesis of a 'toxic' experience, and a strong foundation for improving the chances of a successful psychosocial adjustment, including adequate employment. Investigators believe PREPP holds tremendous promise as an intervention to fill the science-practice gap in the promotion of an optimal emotional environment for the developing infant, particularly for women and children living in poverty and/or facing significant psychosocial hardship.

Locations

Country	Name	City	State
United States	Columbia University Medical Center	New York	New York

Sponsors (2)

Lead Sponsor	Collaborator
New York State Psychiatric Institute	The Robin Hood Foundation

Country where clinical trial is conducted

United States, 

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* Note: There are 60 references in all — Click here to view all references

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in maternal mood and prevalence/severity of postpartum depression.	Investigators will be assessing and tracking the incidence and/or severity of postpartum depression with the use of mood and stress questionnaires (Hamilton Depression Scale, Hamilton Anxiety Scale, Perceived Stress Scale, Center for Epidemiological Studies Depression Scale) administered at 4-6 weeks postpartum, 10 weeks postpartum, and 16 weeks postpartum.	6 weeks postpartum, 10 weeks postpartum, 16 weeks postpartum
Secondary	The effect of behavioral intervention for infants on infant development	Investigators will use neurodevelopmental assessments (Bayley Scale of Infant Development, Still Face Protocol, Free Play Observation, and Conjugate Kicking Task) and cortisol reactivity to assess infant development at 4 months of age.	4 months (infant age)
Secondary	The effect of behavioral intervention on infant sleep and fuss behavior	The infant's sleep and fuss/cry behavior will be assessed at 6 weeks and 16 weeks of age (Baby Day Diary)	6 weeks, 4 months (infant age)