- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04454645
Intervening With Opioid-Dependent MothersMothers and Infants (mABC)
May 2, 2026 updated by: Mary Dozier, University of Delaware
Intervening With Opioid-Dependent Mothers Living in Poverty: Effects on Mothers' and Infants' Behavioral and Biological Regulation
This study will assess the efficacy of the modified Attachment and Biobehavioral Catch-Up (mABC) Intervention, adapted for use with peripartum mothers receiving medication-assisted treatment for opioid use disorder.
The investigators expect that mothers who receive the modified Attachment and Biobehavioral Catch-up Intervention will show more nurturing and sensitive parenting and more adaptive physiological regulation than parents who receive a control intervention.
The investigators expect that infants whose mothers receive the modified Attachment and Biobehavioral Catch-up will show better outcomes in attachment, behavior, and physiological regulation than infants of parents who receive the control intervention.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Pregnant mothers will be randomly assigned to receive the modified ABC intervention or the control intervention (modified DEF).
Hypotheses relate to parent and child outcomes associated with the intervention.
Hypothesis 1: Compared to mothers who receive the control intervention, mothers who receive the mABC intervention will show more nurturing and sensitive parenting, enhanced neural activity during parenting-relevant tasks, and more normative patterns of DNA methylation, autonomic nervous system activity, and cortisol production.
Hypothesis 2: Compared to infants of mothers who receive the control intervention, infants of mothers who receive the mABC intervention will show more organized and secure attachment patterns, better behavioral regulation during stressors, more advanced social-emotional development, and more normative patterns of DNA methylation, autonomic nervous system activity, and cortisol production.
Hypothesis 3: Enhanced maternal sensitivity will mediate effects of the mABC intervention on improved infant outcomes.
Study Type
Interventional
Enrollment (Actual)
174
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 Locations
-
-
Delaware
-
Newark, Delaware, United States, 19716
- University of Delaware
-
-
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
18 years to 70 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Opioid-dependent pregnant women in third trimester of pregnancy on medication-assisted treatment
Exclusion Criteria:
- None
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: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Modified ABC
12-session home visiting intervention designed to increase parental sensitivity and nurturance and decrease parental frightening behavior.
|
Intervention targets parenting sensitivity and nurturance.
|
|
Active Comparator: Modified DEF
12-session home visiting intervention designed to increase parental playful interactions that stimulate infant cognitive and motor development
|
Intervention targets parenting enhancing infant cognitive development
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maternal sensitivity
Time Frame: Pre-intervention (3rd trimester)
|
The mother will be assessed interacting with the infant simulator.
Parental sensitivity (a composite of following the child's lead in interactions, providing nurturance when the child is distressed, and showing positive regard) will be assessed using procedures and coding from the assessment used by the NICHD Study of Early Child Care and Youth Development (Brady-Smith et al., 1999).
Sensitivity will be assessed on a 5-point scale with higher scores indicating greater sensitivity.
|
Pre-intervention (3rd trimester)
|
|
Maternal sensitivity
Time Frame: Infant age of 3 months
|
The mother will be assessed interacting one-to-one with her infant.
Parental sensitivity (a composite of following the child's lead in interactions, providing nurturance when the child is distressed, and showing positive regard) will be assessed using procedures and coding from the assessment used by the NICHD Study of Early Child Care and Youth Development (Brady-Smith et al., 1999).
Sensitivity will be assessed on a 5-point scale with higher scores indicating greater sensitivity.
|
Infant age of 3 months
|
|
Maternal sensitivity
Time Frame: Infant age of 6 months
|
The mother will be assessed interacting one-to-one with her infant.
Parental sensitivity (a composite of following the child's lead in interactions, providing nurturance when the child is distressed, and showing positive regard) will be assessed using procedures and coding from the assessment used by the NICHD Study of Early Child Care and Youth Development (Brady-Smith et al., 1999).
Sensitivity will be assessed on a 5-point scale with higher scores indicating greater sensitivity.
|
Infant age of 6 months
|
|
Maternal sensitivity
Time Frame: Infant age of 12 months
|
The mother will be assessed interacting one-to-one with her infant.
Parental sensitivity (a composite of following the child's lead in interactions, providing nurturance when the child is distressed, and showing positive regard) will be assessed using procedures and coding from the assessment used by the NICHD Study of Early Child Care and Youth Development (Brady-Smith et al., 1999).
Sensitivity will be assessed on a 5-point scale with higher scores indicating greater sensitivity.
|
Infant age of 12 months
|
|
Maternal methylation of μ-opioid receptor (OPRM1) gene
Time Frame: Pre-intervention (3rd trimester)
|
Maternal methylation will be assessed using direct bisulfite sequencing of DNA extracted from saliva
|
Pre-intervention (3rd trimester)
|
|
Maternal methylation of μ-opioid receptor (OPRM1) gene
Time Frame: Infant age of 12 months
|
Maternal methylation will be assessed using direct bisulfite sequencing of DNA extracted from saliva
|
Infant age of 12 months
|
|
Maternal methylation of oxytocin receptor (OXTR) gene
Time Frame: Pre-intervention (3rd trimester)
|
Maternal methylation will be assessed using direct bisulfite sequencing of DNA extracted from saliva
|
Pre-intervention (3rd trimester)
|
|
Maternal methylation of oxytocin receptor (OXTR) gene
Time Frame: Infant age of 12 months
|
Maternal methylation will be assessed using direct bisulfite sequencing of DNA extracted from saliva
|
Infant age of 12 months
|
|
Infant methylation of μ-opioid receptor (OPRM1) gene
Time Frame: Pre-intervention (3rd trimester)
|
Infant methylation will be assessed using direct bisulfite sequencing of DNA extracted from saliva
|
Pre-intervention (3rd trimester)
|
|
Infant methylation of μ-opioid receptor (OPRM1) gene
Time Frame: Infant age of 12 months
|
Infant methylation will be assessed using direct bisulfite sequencing of DNA extracted from saliva
|
Infant age of 12 months
|
|
Maternal neural activity (Event related potentials - ERP) - Own child-other child task
Time Frame: Pre-intervention (3rd trimester)
|
Maternal event-related potentials (ERP) will be assessed while viewing photos of their own infants, familiar infants, and unfamiliar infants.
The P300 (a positive deflection about 300 ms after the stimuli) will be studied, with a bigger difference between own and other child considered preferable.
|
Pre-intervention (3rd trimester)
|
|
Maternal neural activity (Event related potentials - ERP) - Own child-other child task
Time Frame: Infant age of 12 months
|
Maternal event-related potentials will be assessed while viewing photos of their own infants, familiar infants, and unfamiliar infants.
The P300 (a positive deflection about 300 ms after the stimuli) will be studied, with a bigger difference between own and other child considered preferable.
|
Infant age of 12 months
|
|
Maternal neural activity (Event related potentials - ERP) - Reward sensitivity task
Time Frame: Pre-intervention (3rd trimester)
|
Maternal event-related potentials will be assessed while viewing images from four categories: opioid-related images, baby pictures, positive images, and neutral images.
The P300 (a positive deflection about 300 ms after the stimuli) will be studied, with a bigger difference between child and opioid-related images considered preferable.
|
Pre-intervention (3rd trimester)
|
|
Maternal neural activity (Event related potentials - ERP) - Reward sensitivity task
Time Frame: Infant age of 12 months
|
Maternal event-related potentials will be assessed while viewing images from four categories: opioid-related images, baby pictures, positive images, and neutral images.
The P300 (a positive deflection about 300 ms after the stimuli) will be studied, with a bigger difference between child and opioid-related images considered preferable.
|
Infant age of 12 months
|
|
Maternal neural activity (Event related potentials - ERP) - Child emotion task
Time Frame: Pre-intervention (3rd trimester)
|
Maternal event-related potentials will be assessed while viewing images of children crying, laughing, and showing neutral expressions.
The N180 (a negative deflection about 180 ms after the stimuli) will be studied, with a bigger difference between faces will be considered preferable.
|
Pre-intervention (3rd trimester)
|
|
Maternal neural activity (Event related potentials - ERP) - Child emotion task
Time Frame: Infant age of 12 months
|
Maternal event-related potentials will be assessed while viewing images of children crying, laughing, and showing neutral expressions.
The N180 (a negative deflection about 180 ms after the stimuli) will be studied, with a bigger difference between faces will be considered preferable.
|
Infant age of 12 months
|
|
Maternal parasympathetic nervous system activity during Still Face
Time Frame: Pre-intervention (3rd trimester)
|
The control of cardiac functions via the vagal nerve, or vagal tone, is an index of parasympathetic activity.
It can be measured by heart rate variability associated with respiration or high frequency respiratory sinus arrhythmia (RSA).
RSA data will be collected continuously throughout a 15-minute period during the Still Face Procedure using a MindWare Portable Lab system.
Greater changes in RSA from baseline to still face considered preferable.
|
Pre-intervention (3rd trimester)
|
|
Maternal parasympathetic nervous system activity
Time Frame: Infant age of 12 months
|
The control of cardiac functions via the vagal nerve, or vagal tone, is an index of parasympathetic activity.
It can be measured by heart rate variability associated with respiration or high frequency respiratory sinus arrhythmia (RSA).
RSA data will be collected continuously throughout a 15-minute period during the Still Face Procedure using a MindWare Portable Lab system.
Greater changes in RSA from baseline to still face considered preferable.
|
Infant age of 12 months
|
|
Infant parasympathetic nervous system activity
Time Frame: Infant age of 6 months
|
The control of cardiac functions via the vagal nerve, or vagal tone, is an index of parasympathetic activity.
It can be measured by heart rate variability associated with respiration or high frequency respiratory sinus arrhythmia (RSA).
RSA data will be collected continuously throughout a 15-minute period during the Still Face Procedure using a MindWare Portable Lab system.
Greater changes in RSA from baseline to still face considered preferable.
|
Infant age of 6 months
|
|
Infant parasympathetic nervous system activity
Time Frame: Infant age of 12 months
|
The control of cardiac functions via the vagal nerve, or vagal tone, is an index of parasympathetic activity.
It can be measured by heart rate variability associated with respiration or high frequency respiratory sinus arrhythmia (RSA).
RSA data will be collected continuously throughout a 15-minute period during the Still Face Procedure using a MindWare Portable Lab system.
Greater changes in RSA from baseline to still face considered preferable.
|
Infant age of 12 months
|
|
Infant diurnal cortisol production
Time Frame: Infant age of 6 months
|
Infant diurnal cortisol production will be assessed through salivary cortisol levels collected at waketime and bed-time.
|
Infant age of 6 months
|
|
Infant diurnal cortisol production
Time Frame: Infant age of 12 months
|
Infant diurnal cortisol production will be assessed through salivary cortisol levels collected at waketime and bed-time.
|
Infant age of 12 months
|
|
Infant behavioral regulation
Time Frame: Infant age of 6 months
|
Behavioral coding of emotion regulation will be conducted from video recordings of the Still Face Paradigm on the Behavioral Regulation Scale, a mild social stressor.
Behavior regulation will be coded on a scale called Behavior Regulation.
The scores will be continuous with higher scores indicating better regulation (ranging from 1-9).
|
Infant age of 6 months
|
|
Infant behavioral regulation
Time Frame: Infant age of 12 months
|
Behavioral coding of emotion regulation will be conducted from video recordings of the Still Face Paradigm on the Behavioral Regulation Scale, a mild social stressor.
Behavior regulation will be coded on a scale called Behavior Regulation.
The scores will be continuous with higher scores indicating better regulation (ranging from 1-9).
|
Infant age of 12 months
|
|
Infant attachment
Time Frame: Infant age of 12 months
|
Infant attachment will be assessed using the Strange Situation.
Coding will be completed using the standard Strange Situation coding scheme (with 4 major categories, with secure preferable).
|
Infant age of 12 months
|
|
Infant cognitive development
Time Frame: Infant age of 12 months
|
Infant cognitive development will be assessed through maternal report on the Ages and Stages Questionnaire.
Scores could range from 0-300 with higher scores reflecting higher functioning.
|
Infant age of 12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maternal substance use
Time Frame: Pre-intervention (3rd trimester)
|
Mothers will report on substance use through the Timeline Follow-Back Interview.
Higher scores will reflect more use of illicit substances (score from 0-unlimited).
|
Pre-intervention (3rd trimester)
|
|
Maternal substance use
Time Frame: Infant age of 12 months
|
Mothers will report on substance use through the Timeline Follow-Back Interview.
Higher scores will reflect more use of illicit substances (score from 0-unlimited).
|
Infant age of 12 months
|
|
Maternal depression
Time Frame: Pre-intervention (3rd trimester)
|
Mothers will report on their depression on the Beck Depression Inventory - II, with higher scores indicating more depressive symptoms reported.
(Scores could range from 0-63.)
|
Pre-intervention (3rd trimester)
|
|
Maternal depression
Time Frame: Infant age of 12 months
|
Mothers will report on their depression on the Beck Depression Inventory - II, with higher scores indicating more depressive symptoms reported.
(Scores could range from 0-63.)
|
Infant age of 12 months
|
|
Maternal executive functioning
Time Frame: Pre-intervention (3rd trimester)
|
Mothers will complete Flanker task.
Scores have a mean of 100 with a standard deviation of 15, with higher scores reflecting stronger executive functioning.
|
Pre-intervention (3rd trimester)
|
|
Maternal executive functioning
Time Frame: Infant age of 12 months
|
Mothers will complete Flanker task.
Scores have a mean of 100 with a standard deviation of 15, with higher scores reflecting stronger executive functioning.
|
Infant age of 12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Mary Dozier, Ph.D., University of Delaware
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)
May 1, 2020
Primary Completion (Actual)
March 31, 2026
Study Completion (Actual)
March 31, 2026
Study Registration Dates
First Submitted
April 9, 2020
First Submitted That Met QC Criteria
June 27, 2020
First Posted (Actual)
July 1, 2020
Study Record Updates
Last Update Posted (Actual)
May 5, 2026
Last Update Submitted That Met QC Criteria
May 2, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- mABC
- 1R01HD098525-01A1 (U.S. NIH Grant/Contract)
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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