SIESTA-FF: Coparenting, Infant Sleep, and Infant Development

Sponsor
Penn State University (Other)
Overall Status
Recruiting
CT.gov ID
NCT03187561
Collaborator
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) (NIH)
216
1
3
58
3.7

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Infant sleep-adapted coparenting intervention
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
216 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
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.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.
Masking:
Double (Participant, 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.
Primary Purpose:
Prevention
Official Title:
Coparenting, Infant Sleep, and Infant Development
Actual Study Start Date :
May 1, 2018
Anticipated Primary Completion Date :
Feb 28, 2023
Anticipated Study Completion Date :
Feb 28, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Family Foundations (FF)

The original Family Foundations transition-to-parenthood coparenting intervention will be implemented to all participants assigned to this arm

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.

Experimental: Sleep-adapted Family Foundations (FF+)

A sleep-adapted Family Foundations transition-to-parenthood coparenting intervention will be implemented to all participants in this arm. The adaptation will be an emphasis on coparenting in relation to infant sleep concerns and activities.

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.

Other: Control

Participants in this arm will not receive either 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.

Outcome Measures

Primary Outcome Measures

  1. Overall coparenting quality [12 months post-partum]

    Quality of coparenting

  2. Quality of coparenting around infant sleep contexts [1 month post-partum]

    Quality of coparenting regarding decisions parents make about infant sleep

  3. Quality of infant sleep [6 months post-partum]

    Infant sleep quality from actigraphy and infant sleep diaries reported by parents

  4. Quality of parent sleep [6 months post-partum]

    Sleep quality for each parent, from actigraphy and sleep diary information

  5. Attachment Q-Set [12 months post-partum]

    Quality of infant attachment to mother

  6. Attachment Q-Set [12 months post-partum]

    Quality of infant attachment to father

  7. Infant-Toddler Social and Emotional Assessment (ITSEA) [12 months post-partum]

    Behavioral problems and competencies in infants

Secondary Outcome Measures

  1. Maternal depressive symptoms (Beck Depression Inventory) [12 months post-partum]

    Depressive symptoms reported by mothers

  2. Descriptive In-home Survey of Chaos - Observer ReporteD (DISCORD) [1 month post-partum]

    Household chaos, observed, in families

Other Outcome Measures

  1. Paternal depressive symptoms (Beck Depression Inventory) [12 months post-partum]

    Depressive symptoms reported by fathers

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Month to 65 Years
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Douglas Teti State College Pennsylvania United States 16802

Sponsors and Collaborators

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

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Douglas M. Teti, Professor of HDFS, Psychology, and Pediatrics, Penn State University
ClinicalTrials.gov Identifier:
NCT03187561
Other Study ID Numbers:
  • STUDY00006724
  • R01HD088566
First Posted:
Jun 15, 2017
Last Update Posted:
Jun 3, 2021
Last Verified:
Jun 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Douglas M. Teti, Professor of HDFS, Psychology, and Pediatrics, Penn State University

Study Results

No Results Posted as of Jun 3, 2021