Connect to Baby: A Pilot Study of a Parenting and Coparenting Program (CTB)

December 19, 2023 updated by: Rebecca Ryan, Georgetown University

Connect to Baby: A Pilot Study of a Parenting and Coparenting Program for New Parents

The proposed project is a randomized control trial to assess a novel 6-session parenting and coparenting intervention for low-income parents of infants. Connect to Baby (CTB) will be implemented within one of the largest federally-funded early care and education programs, Early Head Start (EHS), in Washington, DC. To engage both fathers and mothers, CTB recruits parents at the time of birth, capitalizing on the "magic moment" of delivery, and uses father-inclusive digital media content to engage men. A key innovation lies in the introduction and rehearsal of four interaction skills -- Noticing, Following, Talking, and Encouraging (NiFTE, pronounced "Nifty") -- to foster serve-and-return interactions with infants as well as supportive, cooperative coparenting interactions between mothers and fathers. To maximize program uptake, CTB is situated within an early education program parents already trust and attend. Additionally, the study will test hybrid program delivery with both in-person and remote sessions using video-enabled tablets to reduce scheduling and logistical barriers and thereby enhance retention. The specific aims of the project are to assess efficacy of random assignment to Hybrid delivery of CTB relative to EHS as usual at enhancing parenting and coparenting quality and parent and child wellbeing. If demonstrated to be efficacious, this program will provide Early Head Start (and other family-serving agencies) a brief cost-effective, manualized preventive intervention that could be used alone or in conjunction with other services to improve parent functioning and co-parenting, further engage fathers in programming and caregiving, and, ultimately, enhance child development.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Overview:

The proposed project is a randomized control trial to assess the effectiveness of a novel 6-session parenting and coparenting intervention for low-income parents of infants designed by the program developers of Just Beginning (JB) and Family Foundations (FF). Connect to Baby (CTB) blends and builds upon these two evidence-based programs and will be implemented within one of the largest federally-funded early care and education programs, Early Head Start (EHS), in Washington, DC. CTB's approach recognizes that although many existing interventions aim to increase parenting quality in low-income contexts, the vast majority yield only modest effects that often fade. These mixed findings stem, in part, from three key weaknesses in existing programs: 1) a focus on mothers, rather than mothers and fathers; 2) a focus on the parent-child relationship to the exclusion of the coparenting relationship; 3) low program recruitment and retention rates. The co-PIs have successfully piloted a program that addresses these weaknesses and can be easily incorporated into programs like EHS to enhance their effects on parenting, and child development. Specifically, to engage both fathers and mothers, CTB recruits parents at the time of birth, capitalizing on the "magic moment" of delivery, and uses father-inclusive digital media content to engage men. A key innovation lies in the introduction and rehearsal of four interaction skills -- Noticing, Following, Talking, and Encouraging (NiFTE, pronounced "Nifty") -- to foster serve-and-return interactions with infants as well as supportive, cooperative coparenting interactions between mothers and fathers. To maximize program uptake, CTB is situated within an early education program parents already trust and attend. Additionally, the study will test hybrid program delivery with both in-person and remote sessions using video-enabled tablets to reduce scheduling and logistical barriers and thereby enhance retention. CTB has two key targets of intervention - coparenting communication and parenting quality. By enhancing these targets, CTB aims to improve parent mental health, and child socioemotional and language outcomes. The specific aims of the project are to assess efficacy of random assignment to Hybrid delivery of CTB relative to EHS as usual at enhancing program targets and both parent mental health and infant socioemotional and language outcomes. If demonstrated to be efficacious, this program will provide Early Head Start (and other family-serving agencies) a brief cost-effective, manualized preventive intervention that could be used alone or in conjunction with other services to improve parent functioning and co-parenting, further engage fathers in programming and caregiving, and, ultimately, enhance child development.

Families will be randomly assigned to CTB-EHS Hybrid and EHS-digital only conditions. There will be 100 dyads randomly assigned to each condition. The main objective of the study is to test the feasibility of the CTB-Hybrid intervention for enhancing targets of co-parenting and parenting, and outcomes of parent well-being and child language and socioemotional development. The specific aims are:

Aim 1. To assess the efficacy of CTB-Hybrid at improving program targets. One hundred and fifty families will be recruited and randomized to one of two conditions: 1) EHS-CTB Hybrid or 2) EHS-digital with CTB digital content (content delivered via the customized application). CTB is hypothesized to increase coparenting communication quality and parenting quality relative to EHS digital at 3- and 6-months post-random assignment (RA); comparing results at each time point will distinguish immediate from sustained effects of the program. Analyses will include both intent-to-treat (ITT) and treatment-on-the-treated (TOT) analyses to determine the importance of program dosage for program efficacy.

Aim 2. To assess the efficacy of CTB-Hybrid at enhancing secondary program outcomes. CTB will also be assessed with regard to parent mental health (assessed using parent self-report and a short diagnostic interview at 3- and 6-months post (RA), and child socioemotional and language outcomes at 3- and 6-months post RA (assessed using parent-report and objective ratings). In exploratory analyses, parenting and coparenting quality will be tested as mediators and child sex as moderator of effects on secondary outcomes.

Study Site:

13 EHS centers in the Washington DC region.

Recruitment, Screening, Enrollment and Informed Consent:

Participants will be recruited at the EHS centers. Informed consent will be collected remotely via zoom and using REDCAP. Given our experiences during the COVID pandemic we will also collect pre and post measures remotely via zoom. For assessment, EHS-digital only and CTB-hybrid families will pick up a packet from the EHS center that includes a data enabled tablet with a zoom link and links to REDCAP survey links and surveys completed on the tablet and a standard set of toys for the assessment. The materials will be returned to the center after the assessment is complete. Except for the child language measure, MCDI, all measures will be administered at each of the three assessment time points. Mindful of the potential burden of lengthy assessments for this high-risk population, assessments will be administered via two Zoom calls that can be done via mobile phone or tablet separated by one week if needed or requested. Non-proprietary measures will be entered into REDCAP and administered on a tablet or mobile phone.

Study Procedures and Evaluations:

Overall study duration and duration of participant involvement. The intervention is 10 weeks long. Participants will also be involved in a pre-assessment, a post-assessment (3 months post random assignment) and a follow-up (6 months post random assignment)

Retention of Study Subjects:

The hybrid delivery is linked to a trusted service (EHS) and the hybrid delivery allows for flexibility in scheduling.

Fidelity Monitoring:

Each CTB facilitator will participate in a two-day training to learn to use the manual and understand the program's principles and how to effectively use the technology to deliver the content remotely run by the lead CTB facilitator. Once facilitators complete training, the first six sessions each facilitator delivers will be video-recorded, via zoom, for fidelity review. During implementation, every 10th session will be recorded and reviewed for fidelity. The trainer, an LCSW will provide individual and group feedback on the extent to which the facilitator followed the manual and engaged parents effectively. Feedback will be based on video review and a fidelity coding scheme created for CTB in which facilitators are scored for session component completion, and 7 positive engagement, 7 negative engagement criteria, every 30 seconds. Pilot data showed that reliability on the fidelity scheme was high (kappa > .7) as was session fidelity and facilitator quality, with low levels of negative engagement and high levels of positive engagement. Any facilitator not delivering CTB with fidelity will receive a refresher training. Moreover, a clinical supervisor and trainer will be available via phone.

Study Type

Interventional

Enrollment (Estimated)

200

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • District of Columbia
      • Washington, District of Columbia, United States, 20057
        • Recruiting
        • Child Development and Social Policy Lab
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Must be a mother, father (or father figure, including same sex parent and grandparent) of an infant who is 2-24 months.
  • Must speak and read English or Spanish with sufficient fluency for completion of consent forms and questionnaires and actively participate in the intervention.

Exclusion Criteria:

• Pre-intervention assessment their score on the Woman Abuse Screening Tool (WAST) Interpersonal Violence (IPV) screener (Brown, Lent, Schmidt, & Sas, 2000) indicates sexual or physical abuse.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: EHS-CTB Hybrid
Dyads in the EHS-CTB hybrid condition will receive 6 individual sessions of CTB conducted by trained facilitators. The first session would be at the center, the 2nd through 5th would be remote, and 6th would be at the EHS center as a group session with other families. Sessions will occur approximately one to two weeks apart, allowing for program completion within 10 weeks. During the first in-person session, families will receive tablets with data plans and with the Zoom. They will receive a welcome pack that includes baby gifts that are used to support each session.
To engage both fathers and mothers, CTB recruits parents at the time of birth, capitalizing on the "magic moment" of delivery, and uses father-inclusive digital media content to engage men. A key innovation lies in the introduction and rehearsal of four interaction skills -- Noticing, Following, Talking, and Encouraging (NiFTE, pronounced "Nifty") -- to foster serve-and-return interactions with infants as well as supportive, cooperative coparenting interactions between mothers and fathers. To maximize program uptake, CTB is situated within an early education program parents already trust and attend. Additionally, the study will test hybrid program delivery with both in-person and remote sessions using video-enabled tablets to reduce scheduling and logistical barriers and thereby enhance retention.
No Intervention: EHS-CTB Digital Only
Dyads in the EHS-CTB digital only group will receive EHS early education, as well as EHS home visitation, and will have access to the CTB content via text messages, but will receive no CTB sessions. Digital content includes videos of Baby Elmo and his father and suggested activities.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Parent Acceptance/Warmth during parent-child interactions
Time Frame: At baseline (when families are enrolled in the study)
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
At baseline (when families are enrolled in the study)
Parent Acceptance/Warmth during parent-child interactions
Time Frame: 3 months
Qualitative rating (0-4 scale) as coded from a 25 minute parent-child interaction
3 months
Parent Acceptance/Warmth during parent-child interactions
Time Frame: 6 months
Positive parenting behaviors as coded from a 25 minute parent-child interaction
6 months
Parent Descriptive Language during parent-child interactions
Time Frame: At baselined (when families enroll in the study)
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
At baselined (when families enroll in the study)
Parent Descriptive Language during parent-child interactions
Time Frame: 3 months
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
3 months
Parent Descriptive Language during parent-child interactions
Time Frame: 6 months
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
6 months
Parent Follows child's lead during parent-child interactions
Time Frame: At baseline (when families enroll in the study)
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
At baseline (when families enroll in the study)
Parent Follows child's lead during parent-child interactions
Time Frame: 3 months
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
3 months
Parent Follows child's lead during parent-child interactions
Time Frame: 6 months
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
6 months
Parent Extends Child's Focus during parent-child interactions
Time Frame: At baseline (when families enroll in the study
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
At baseline (when families enroll in the study
Parent Extends Child's Focus during parent-child interactions
Time Frame: 3 months
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
3 months
Parent Extends Child's Focus during parent-child interactions
Time Frame: 6 months
Qualitative rating (0-4 scale) as coded from a 25 minute parent-child interaction
6 months
Parent restricts child during parent-child interactions
Time Frame: At baseline (when families enroll in the study)
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
At baseline (when families enroll in the study)
Parent restricts child during parent-child interactions
Time Frame: 3 months
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
3 months
Parent restricts child during parent-child interactions
Time Frame: 6 months
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
6 months
Parent criticizes child during parent-child interactions
Time Frame: At baseline (when families enroll in the study)
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
At baseline (when families enroll in the study)
Parent criticizes child during parent-child interactions
Time Frame: 3 months
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
3 months
Parent criticizes child during parent-child interactions
Time Frame: 6 months
Qualitative rating (0-4 scale) of as coded from a 25 minute parent-child interaction
6 months
Coparenting Quality:mother-father pleasure in coparenting
Time Frame: At baseline (when families enroll in the study)
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
At baseline (when families enroll in the study)
Coparenting Quality:mother-father pleasure in coparenting
Time Frame: 3 months
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
3 months
Coparenting Quality:mother-father pleasure in coparenting
Time Frame: 6 months
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
6 months
Coparenting Quality: displeasure in coparenting
Time Frame: At baseline (when families enroll in the study)
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
At baseline (when families enroll in the study)
Coparenting Quality: displeasure in coparenting
Time Frame: 3 months
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
3 months
Coparenting Quality: displeasure in coparenting
Time Frame: 6 months
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
6 months
Coparenting Quality: interactiveness
Time Frame: at baseline (when families enroll in the study)
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
at baseline (when families enroll in the study)
Coparenting Quality: interactiveness
Time Frame: 3 months
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
3 months
Coparenting Quality: interactiveness
Time Frame: 6 months
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
6 months
Coparenting Quality: cooperation
Time Frame: At baseline (when families enroll in the study)
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
At baseline (when families enroll in the study)
Coparenting Quality: cooperation
Time Frame: 3 months
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
3 months
Coparenting Quality: cooperation
Time Frame: 6 months
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
6 months
Coparenting Quality: competition
Time Frame: At baseline (when families enroll in the study)
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
At baseline (when families enroll in the study)
Coparenting Quality: competition
Time Frame: 3 months
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
3 months
Coparenting Quality: competition
Time Frame: 6 months
Qualitative rating scale (1-5) as coded from a 25 minutes mother-father-child interaction
6 months
Coparenting Relationship Scale
Time Frame: At baseline (when families enroll in the study)
Coparenting relationship scale measuring quality of communication, 14 items, scale 1-6.
At baseline (when families enroll in the study)
Coparenting Relationship Scale
Time Frame: 3 months
Coparenting relationship scale measuring quality of communication, 14 items, scale 1-6.
3 months
Coparenting Relationship Scale
Time Frame: 6 months
Coparenting relationship scale measuring quality of communication, 14 items, scale 1-6.
6 months
Father Engagement Scale
Time Frame: At baseline (when families enroll in the study)
Father Engagement Scale, measuring fathers' engagement in 11 activities with infants, scale 0 - 4
At baseline (when families enroll in the study)
Father Engagement Scale
Time Frame: 3 months
Father Engagement Scale, measuring fathers' engagement in 11 activities with infants, scale 0 - 4
3 months
Father Engagement Scale
Time Frame: 6 months
Father Engagement Scale, measuring fathers' engagement in 11 activities with infants, scale 0 - 4
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Parent mental health
Time Frame: At baseline (when families enroll in the study)
Center for Epidemiologic Studies Depression Scale Revised, scale to measure parent depression symptoms (10-items), scale 0 - 3
At baseline (when families enroll in the study)
Parent mental health
Time Frame: 3 months
Center for Epidemiologic Studies Depression Scale Revised, scale to measure parent depression symptoms (10-items), scale 0 - 3
3 months
Parent mental health
Time Frame: 6 months
Center for Epidemiologic Studies Depression Scale Revised, scale to measure parent depression symptoms (10-items), scale 0 - 3
6 months
Parent self efficacy
Time Frame: at baseline (when families enroll in the study)
Parental Sense of Competence Scale, 17 items, scale 1 - 6
at baseline (when families enroll in the study)
Parent self efficacy
Time Frame: 3 months
Parental Sense of Competence Scale, 17 items, scale 1 - 6
3 months
Parent self efficacy
Time Frame: 6 months
Parental Sense of Competence Scale, 17 items, scale 1 - 6
6 months
Child language development
Time Frame: At baseline (when families enroll in the study)
Videotaped parent-infant play task coded using the family interactions using the Individual Growth and Development Indicators (IGDI) Early Communication Indicator (ECI), which codes expressive communication for children between 3 and 36 months.
At baseline (when families enroll in the study)
Child language development
Time Frame: 3 months
Videotaped parent-infant play task coded using the family interactions using the Individual Growth and Development Indicators (IGDI) Early Communication Indicator (ECI), which codes expressive communication for children between 3 and 36 months.
3 months
Child language development
Time Frame: 6 months
Videotaped parent-infant play task coded using the family interactions using the Individual Growth and Development Indicators (IGDI) Early Communication Indicator (ECI), which codes expressive communication for children between 3 and 36 months.
6 months
Child socioemotional development
Time Frame: at baseline (when families enroll in the study)
The Brief Infant Toddler Social Emotional Assessment (BITSEA), which assesses behavior problems and competencies, 42 items, scale 0 - 2
at baseline (when families enroll in the study)
Child socioemotional development
Time Frame: 3 months
The Brief Infant Toddler Social Emotional Assessment (BITSEA), which assesses behavior problems and competencies, 42 items, scale 0 - 2
3 months
Child socioemotional development
Time Frame: 6 months
The Brief Infant Toddler Social Emotional Assessment (BITSEA), which assesses behavior problems and competencies, 42 items, scale 0 - 2
6 months
Parent Generalized Anxiety Scale
Time Frame: At baseline (when families enroll in the study)
Scale to measure parent anxiety, Generalized Anxiety Scale, 7 items, scale 0 - 3
At baseline (when families enroll in the study)
Parent Generalized Anxiety Scale
Time Frame: 3 months
Scale to measure parent anxiety, Generalized Anxiety Scale, 7 items, scale 0 - 3
3 months
Parent Generalized Anxiety Scale
Time Frame: 6 months
Scale to measure parent anxiety, Generalized Anxiety Scale, 7 items, scale 0 - 3
6 months
Child Language Development
Time Frame: 3 months
Scale measuring child expressive and receptive language development, MacArthur-Bates Communicative Development Inventories (MCDI) for infants/toddlers, 89-word vocabulary checklist, 0 - 178 (each item has 0 - 2 scale)
3 months
Child Language Development
Time Frame: 6 months
Scale measuring child expressive and receptive language development, MacArthur-Bates Communicative Development Inventories (MCDI) for infants/toddlers, 89-word vocabulary checklist, 0 - 178 (each item has 0 - 2 scale)
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Rebecca Ryan, PhD, Georgetown University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2023

Primary Completion (Estimated)

October 31, 2024

Study Completion (Estimated)

December 31, 2024

Study Registration Dates

First Submitted

May 18, 2023

First Submitted That Met QC Criteria

December 19, 2023

First Posted (Actual)

December 22, 2023

Study Record Updates

Last Update Posted (Actual)

December 22, 2023

Last Update Submitted That Met QC Criteria

December 19, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • R21HD108499 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

This application requests support to collect and maintain a database of contact information, pre- and post-random assignment interview and video records for 200 participants and session recordings for 100 participants for supervision and fidelity tracking. Georgetown University Psychology department will serve as the Data Coordinating Center for this project, utilizing the REDCap database system for secure storage and sharing of research data. Video records will be securely stored and shared on Databrary (www.databrary.org), which is a video repository. While video records require explicit permission, deidentified datasets can also be made available in shared volumes on Databrary and on the open science framework https://osf.io/ to increase accessibility to non-clinical researchers.

IPD Sharing Time Frame

Data will be made available 12 months after the study completion date.

IPD Sharing Access Criteria

The deidentified data will be available to any researchers with access to Databrary or OSF.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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