Promoting Co-Parenting and Reducing Hazardous Drinking in New Families

Sponsor
Penn State University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04441307
Collaborator
Rochester Institute of Technology (Other), University at Buffalo (Other), National Institute on Alcohol Abuse and Alcoholism (NIAAA) (NIH)
360
2
2
39.1
180
4.6

Study Details

Study Description

Brief Summary

This study aims to understand if a parenting program that helps couples learn to parent as a team and maintain a healthy lifestyle, such as maintaining safer levels of alcohol use, promotes parent and child health and well-being. Programs will be delivered prenatally and postnatally and will include both group classes and individualized sessions. A comprehensive assessment is administered during pregnancy and then at 6 and 12 months of child age. It is hypothesized that targeting intervention during the naturally motivating transition to parenthood may not only provide opportunities for long lasting behavioral change for parents, but also initiate a cascade of protective processes that ultimately reduce risk for negative emotional and behavioral outcomes for children.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Healthy Foundations
  • Behavioral: Family Foundations
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
360 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
In both arms, couples will experience a parenting program for expecting first time parents. In one arm, parents will receive an adapted Family Foundations program. In the other arm, parents will receive an empirically supported community parenting program.In both arms, couples will experience a parenting program for expecting first time parents. In one arm, parents will receive an adapted Family Foundations program. In the other arm, parents will receive an empirically supported community parenting program.
Masking:
Double (Participant, Outcomes Assessor)
Masking Description:
Participants will be asked to participate in a parenting program but will not be informed about which arm of the study they have been assigned. To avoid bias in the evaluation of the interventions, outcome assessors will not be informed about which arm of the study participants have been assigned.
Primary Purpose:
Prevention
Official Title:
Strong Foundations: Intervening to Promote Co-Parenting and Reduce Father Hazardous Drinking in Expectant Parents
Actual Study Start Date :
Jan 25, 2021
Anticipated Primary Completion Date :
Apr 30, 2024
Anticipated Study Completion Date :
Apr 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Healthy Foundations

A community-based parenting education program with individual family check ins will be implemented to all participants assigned to this arm.

Behavioral: Healthy Foundations
Healthy Foundations combines elements of a community-based parent education program with additional information about infant and child development, good parenting practices, parent health behavior, and couple support.

Experimental: Family Foundations

An adapted Family Foundations parenting program for expecting first time parents with individual family check ins will be implemented to all participants assigned to this arm.

Behavioral: Family Foundations
A modified version of Family Foundations, an evidence-based preventive intervention for couples during the transition to parenthood, will be implemented to address several aspects of parent and family adjustment, including parent health behavior, particularly alcohol use, and couple relationship dynamics, to promote a healthy parenting environment.

Outcome Measures

Primary Outcome Measures

  1. Couple Relationship/Co-parenting [6 months of child age]

    Couple relationship will be evaluated through the Co-parenting Relationship Scale. For overall coparenting quality, average responses range from 0 (not true of us/never) to 6 (very true of us/very often). Lower scores indicate worse outcomes.

  2. Parent Adjustment [6 months of child age]

    Parent adjustment will be assessed with self-report on mental health screenings. The Brief Symptom Inventory is a widely used mental health screening measure. Average responses to the listed symptoms range from 0 (not at all) to 4 (extremely) based on how distressing symptoms have been. Higher scores indicate greater intensity of symptoms.

  3. Parent Alcohol Use [6 months of child age]

    Quantity-frequency of alcohol use (Quantity Frequency Index) and frequency of binge drinking (4 or 5 or more on a single occasion) based on the NIAAA standard drink will be assessed. Higher scores indicate greater quantity and frequency of alcohol use and binge drinking, with moderate drinking being defined as up to 1 standard drink per day for women and up to 2 standard drinks per day for men.

Secondary Outcome Measures

  1. Parent-infant Interactions [6 and 12 months of child age]

    Parent-child relations will be measured through the coding of play interaction sessions. Parental warmth, sensitivity, and harshness will be coded during parent-infant interactions. Parents will be asked to spend some time with their infants as they normally would at 6 months. At 12 months, parents will be asked to spend some time with infants as they normally would for the first 5 minutes, and given a series of problem-solving tasks to do with their infants for the next 5 minutes. Warmth (positive affective involvement), sensitivity (e.g., flexibility and contingent responsiveness), and harshness (e.g., intrusive and negative behaviors such as angry/hostile mood and voice, disapproval, and criticism) will be coded based on the global 5-point rating scales of the Early Relational Assessment (Clark, 1999). Higher scores on the rating scales indicate higher frequency of warmth, sensitivity, and harshness.

  2. Infant Self-Regulation [6 and 12 months of child age]

    The Revised Infant Behavior Questionnaire (IBQ-R, Gartstein & Rothbart, 2003) will be used to obtain parent reports of infant reactivity/regulation at 6 and 12 months of infant ages. The scale measures three broad dimensions of behavior Surgency/Extraversion, Negative Affectivity, and Orienting/Regulation. The Surgency/Extraversion dimension includes approach, vocal reactivity, high intensity pleasure, smiling and laughter, activity level, and perceptual sensitivity. The Negative Affectivity dimension includes sadness, distress to limitations, fear, and low falling reactivity. The Orienting/Regulation dimension includes low intensity pleasure, cuddliness, duration of orienting, and soothability. Scores range from 1-7 and higher scores on each dimension reflect higher surgency, negative affect, and regulation. Average of maternal and paternal scores on these three broad dimensions will be included as the final outcome measures.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Pregnant couples who are cohabitating

  • Parents are 18 years of age or older

  • Health behavior such as moderate to heavy drinking

  • English speaking

Exclusion Criteria:
  • Plural pregnancy

  • Illicit drug use other than cannabis for either parent

Contacts and Locations

Locations

Site City State Country Postal Code
1 University at Buffalo Buffalo New York United States 14260
2 Rochester Institute of Technology Henrietta New York United States 14467

Sponsors and Collaborators

  • Penn State University
  • Rochester Institute of Technology
  • University at Buffalo
  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Investigators

  • Principal Investigator: Rina D Eiden, PhD, Penn State
  • Principal Investigator: Stephanie Godleski, PhD, Rochester Institute of Technology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Rina D. Eiden, Professor of Psychology, Penn State University
ClinicalTrials.gov Identifier:
NCT04441307
Other Study ID Numbers:
  • STUDY00003112
  • 7R01AA027708-02
  • SITE00000607,
First Posted:
Jun 22, 2020
Last Update Posted:
Apr 1, 2022
Last Verified:
Mar 1, 2022
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 Rina D. Eiden, Professor of Psychology, Penn State University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 1, 2022