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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03187561
Other study ID # STUDY00006724
Secondary ID R01HD088566
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date November 15, 2018
Est. completion date March 31, 2023

Study information

Verified date September 2022
Source Penn State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This 3-arm RCT tests the effects of a sleep-enhanced adaptation (FF+) of a well-known, evidence-based transition-to-parenting coparenting intervention program (Family Foundations; FF). In one arm, families will experience FF as originally formulated; in the second, families will receive an adapted FF (FF+) program that emphasizes coparenting in infant sleep contexts; the third arm will serve as controls. It is hypothesized that (1) Compared to controls, parents in both FF groups will report improved overall coparenting and reduced overall distress, but parents in the FF+ group will show greater improvements in coparenting and individual parenting in infant sleep contexts, better infant and parent sleep, and better child adjustment; (2) early coparenting around infant sleep will be a central mechanism by which both interventions exert their effects.


Description:

Although infant sleep regulation across the first year proceeds well for many infants, for many infants that is not the case, and estimates of sleep problems among infants and preschoolers range between 25%-33%. Dysregulated infant sleep is predictive of poor parent sleep, and chronic sleep disruption can place families in turmoil, with consequences for the marital and coparenting relationship. Further, mothers reporting early coparenting distress are at risk for personal distress and poor bedtime and nighttime parenting, which in turn predicts infant sleep problems and insecure infant attachment. This application proposes a randomized clinical trial (RCT) to evaluate the effects of a sleep-enhanced adaptation of an evidence-based transition-to-parenting coparenting intervention program [Family Foundations - FF). The rationale for this study is twofold. First, recent findings from the PI's Project SIESTA (R01HD052809) indicate that poor coparenting at one month post-partum predicts persistent infant-parent co-sleeping across the first year, elevated maternal depressive symptoms, emotionally unavailable bedtime parenting, and insecure infant-mother attachments. Second, whereas FF as originally developed has been successful in improving coparenting, marital adjustment, and overall parenting quality, it gives little specific attention to coparenting in infant sleep contexts, which SIESTA findings identify as critically important to parent and infant outcomes later in the first year. The proposed 3-arm RCT responds to these concerns. In one arm, families will experience FF as originally formulated; in the second, families will receive an adapted FF that emphasizes coparenting in infant sleep contexts; the third arm will serve as controls. Assessments of coparenting and parenting in infant sleep contexts, parental adjustment to infant sleep behavior, choices about sleep arrangements, infant and parent sleep quality, and infant socio-emotional functioning, will serve as outcomes. Our central hypotheses are: (1) Compared to controls, parents in both FF groups will report improved overall coparenting and reduced overall distress, but parents in the adapted FF group will show greater improvements in coparenting and individual parenting in infant sleep contexts, better infant and parent sleep, and better child adjustment; (2) early coparenting around infant sleep will be a central mechanism by which both interventions exert their effects. This research is foundational to a broader understanding of coparenting processes that underlie successful family transitions and contributes to the refinement of a successful coparenting program. Study results will be of immediate use to obstetric and pediatric services interested in augmenting childbirth education material with information on coparenting practices in infant sleep contexts.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 216
Est. completion date March 31, 2023
Est. primary completion date March 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 1 Month to 65 Years
Eligibility Inclusion Criteria: - Two-parent families (married or living with a partner - Families pregnant with their first child, of any race/ethnicity - Parents who can understand and speak English - Parents over the age of 18 - Parents living in independent units Exclusion Criteria: - Single-parent families - Families pregnant with a second born or later born child - Families who cannot speak and understand English - Families in which one parent under the age of 18 - Parents living with families of origin

Study Design


Intervention

Behavioral:
Infant sleep-adapted coparenting intervention
The Family Foundations intervention, as originally formulated, and a sleep-adapted Family Foundations intervention, will be implemented to participants in arm 1 and arm 2, respectively.

Locations

Country Name City State
United States Douglas Teti State College Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
Penn State University Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Paternal depressive symptoms (Beck Depression Inventory) Depressive symptoms reported by fathers 12 months post-partum
Primary Overall coparenting quality Quality of coparenting 12 months post-partum
Primary Quality of coparenting around infant sleep contexts Quality of coparenting regarding decisions parents make about infant sleep 1 month post-partum
Primary Quality of infant sleep Infant sleep quality from actigraphy and infant sleep diaries reported by parents 6 months post-partum
Primary Quality of parent sleep Sleep quality for each parent, from actigraphy and sleep diary information 6 months post-partum
Primary Attachment Q-Set Quality of infant attachment to mother 12 months post-partum
Primary Attachment Q-Set Quality of infant attachment to father 12 months post-partum
Primary Infant-Toddler Social and Emotional Assessment (ITSEA) Behavioral problems and competencies in infants 12 months post-partum
Secondary Maternal depressive symptoms (Beck Depression Inventory) Depressive symptoms reported by mothers 12 months post-partum
Secondary Descriptive In-home Survey of Chaos - Observer ReporteD (DISCORD) Household chaos, observed, in families 1 month post-partum
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