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Coparenting, Infant Sleep, and Infant Development

Coparenting, Infant Sleep, and Infant Development

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03187561
Acronym
SIESTA-FF
Enrollment
216
Registered
2017-06-15
Start date
2018-11-15
Completion date
2025-05-09
Last updated
2025-05-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Marital Relationship, Parent-Child Relations, Parenting, Sleep

Keywords

Sleep, Parenting, Marital relationship, Parent-child relations

Brief 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.

Detailed 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.

Interventions

BEHAVIORALInfant 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.

Sponsors

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

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

All participants will be informed that they are being recruited into an intervention study targeting coparenting, but participants will not be informed about which arm of the study to which they have been assigned. Data collectors and outcome assessors will not be informed about which arm of the study to which participants have been assigned, to assure that all outcomes and evaluations of intervention are conducted blindly, to avoid experimenter bias.

Intervention model description

In the proposed 3-arm RCT, in one arm families will experience Family Foundations (FF) intervention 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.

Eligibility

Sex/Gender
ALL
Age
1 Months to 65 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Infant-Toddler Social and Emotional Assessment (ITSEA)12 months post-partumBehavioral problems and competencies in infants
Quality of infant sleep6 months post-partumInfant sleep quality from actigraphy and infant sleep diaries reported by parents
Quality of parent sleep6 months post-partumSleep quality for each parent, from actigraphy and sleep diary information
Attachment Q-Set12 months post-partumQuality of infant attachment to mother
Overall coparenting quality12 months post-partumQuality of coparenting
Quality of coparenting around infant sleep contexts1 month post-partumQuality of coparenting regarding decisions parents make about infant sleep

Secondary

MeasureTime frameDescription
Maternal depressive symptoms (Beck Depression Inventory)12 months post-partumDepressive symptoms reported by mothers
Descriptive In-home Survey of Chaos - Observer ReporteD (DISCORD)1 month post-partumHousehold chaos, observed, in families

Other

MeasureTime frameDescription
Paternal depressive symptoms (Beck Depression Inventory)12 months post-partumDepressive symptoms reported by fathers

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026