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Behavioral Intervention

Infant sleep-adapted coparenting intervention for Parenting (SIESTA-FF Trial)

N/A

Waitlist Available

Research Sponsored by Penn State University

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Timeline

Screening 3 weeks

Treatment Varies

Follow Up 12 months post-partum

Awards & highlights

SIESTA-FF Trial Summary

This trial is testing whether an adaptation of a well-known parenting intervention that emphasizes coparenting in infant sleep contexts leads to better outcomes than the original intervention or no intervention at all.

Eligible Conditions

Parenting
Sleep
Marital Relationships
Parent-Child Relationship

SIESTA-FF Trial Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ 12 months post-partum

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~12 months post-partum

This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 months post-partum for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Attachment Q-Set

Infant-Toddler Social and Emotional Assessment (ITSEA)

Overall coparenting quality

+3 more

Secondary outcome measures

Descriptive In-home Survey of Chaos - Observer ReporteD (DISCORD)

Maternal depressive symptoms (Beck Depression Inventory)

Other outcome measures

Paternal depressive symptoms (Beck Depression Inventory)

SIESTA-FF Trial Design

3Treatment groups

Experimental Treatment

Group I: Sleep-adapted Family Foundations (FF+)Experimental Treatment1 Intervention

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.

Group II: Family Foundations (FF)Experimental Treatment1 Intervention

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

Group III: ControlExperimental Treatment1 Intervention

Participants in this arm will not receive either intervention.

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Who is running the clinical trial?

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)NIH

1,964 Previous Clinical Trials

2,672,343 Total Patients Enrolled

20 Trials studying Parenting

6,547 Patients Enrolled for Parenting

Penn State UniversityLead Sponsor

355 Previous Clinical Trials

125,541 Total Patients Enrolled

3 Trials studying Parenting

710 Patients Enrolled for Parenting

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is there an eligibility criteria for participation in this trial?

"Prerequisites for partaking in this medical experiment include a minimum age of 1 Month and maximum age of 65. In total, 216 candidates are being sought out to complete the trial."

Answered by AI

Are new participants still welcome to join this research endeavor?

"Clinicaltrials.gov reveals that this medical research experiment, first posted on November 15th 2018 and last modified on September 26th 2022, is no longer recruiting patients. However, there are currently 275 other clinical trials actively looking for participants."

Answered by AI

Does this experiment accept individuals who are below the age of thirty?

"Participants in this trial must fall within the age range of 1 Month to 65. There are 117 clinical trials designed for people younger than 18 years of age and 172 studies available for those over 65."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

Coparenting, Infant Sleep, and Infant Development

Douglas M. Teti 2018. "Coparenting, Infant Sleep, and Infant Development". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT03187561.