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Enrolling by invitationNCT06732310Updated Apr 23, 2026

The Unique and Combined Effects of Prenatal and Early Childhood Programming on Child Maltreatment: Examining Mechanisms of Change

A Phase 2 interventional study of Pregnant Moms' Empowerment Program and Reminiscing and Emotion Training in Child Abuse, Intimate Partner Violence and Secondary Prevention, sponsored by University of Notre Dame. Enrolling by invitation at 2 sites in United States. Open to participants aged 3 Years and older. Per ClinicalTrials.gov, last updated 2026-04-23.

Sponsored by University of Notre Dame · Phase 2, Interventional, and Prevention

Phase
Phase 2
Study type
Interventional
Enrollment
600
Allocation
Randomized
Ages
3 Years and older
Sex
All
01

Study summary

Child maltreatment and child exposure to adult intimate partner violence (IPV) often co-occur and are detrimental to the mental and physical health of children, yet few prevention programs address these intersecting forms of adversity using dual-generation approaches. The proposed study is a rigorous randomized controlled trial that uses a 2x2 factorial design to evaluate the potential synergistic benefits of delivering programming prenatally and during early childhood in order to support the mother-child relationship and ultimately prevent child maltreatment. If effective in preventing child maltreatment, these programs have the potential for high public health impact given that they are both cost-effective and readily scalable.

Read the detailed description

The study will occur at two sites - the University of Notre Dame and the University of Memphis. A total of N=300 mother-child dyads will participate, with an equal number of dyads drawn from each site - Memphis, TN (n=115) and South Bend, IN (n=115). The sample will be composed of n=230 women and children drawn from an ongoing randomized clinical trial (RCT) of the PMEP (R01HD098092); during Year 1 of the current study, we will implement the PMEP RCT protocol with an additional n=70 women, for a total sample of N=300 families.

In order to be eligible for the PMEP trial arm, women must be: 18 years or older, pregnant (between 10 and 30 weeks), English speaking, and exposed to IPV in the past year. To be eligible for re-enrollment in the RET trial arm, women must have previously participated in the PMEP trial arm. Women who have a significant mental health disorder or cognitive impairment that precludes their ability to understand or participate in the intervention will be excluded. Mothers who have experienced miscarriage, infant death, or who no longer have custody of the child with whom they were pregnant with when they participated in the PMEP trial arm will be excluded from the intervention given that the RET trial arm requires active participation from both parent and child; if mothers, however, have had another child who was born after PMEP who is in the eligible age range, they may participate.

The primary objective of the current study is to evaluate the unique and combined effects of evidence-based prenatal (i.e., Pregnant Moms' Empowerment Program) and early childhood (i.e., Reminiscing and Emotion Training) programming to prevent child maltreatment.

Study hypotheses are tested in a 2x2 randomized controlled trial design, with four conditions: PMEP + early childhood control, PMEP + RET, prenatal control + RET, or prenatal and early childhood controls.

Enrollment will continue for approximately 3.5 years, with an expected enrollment rate of approximately 8 mother-child dyads per month. For mother-child dyads who participated in the RCT of the PMEP (n = 230) the expected duration of the RET arm will be approximately 11 months. For the mother-child dyads who will be newly enrolled into the PMEP trial arm as part of the proposed study, the expected duration of the PMEP arm is 16 months; when these children are 3-6 years old, they will participate in the RET arm for 11 months.

Women and children newly enrolled in the PMEP trial arm as part of the current study will complete eight assessments. These will include four PMEP trial arm assessments (baseline [T1], post-test [T2], 3 month post-partum follow-up [T3], and 12 month post-partum follow-up [T4]) and four more assessments (baseline [T5], post-test [T6], 3 month follow-up [T7], 6 month follow-up [T8]) completed as part of the RET trial arm. Dyads only participating in the RET trial arm will participate in the 4 RET assessments (i.e., T5-T8). Women will be compensated for each assessment and children will receive a small toy.

Primary outcome measures will include DCS records (gathered at T5, T8, and 12 month follow-up) coded using the Maltreatment Classification System, the Maternal Maltreatment Classification Interview, the Adult Adolescent Parenting inventory, the Child Abuse Potential Inventory, the Revised Conflict Tactics Scale, and Maternal Sensitivity (coded from observational data). A number of covariates will also be collected, including maternal mental health, childhood trauma and traumatic/major life events over the study period, child exposure to other forms of violence, child temperament, and social support.

For women randomized to receive the PMEP intervention, participation will include five group sessions that utilize interactive learning and group-based discussion to empower women to end intergenerational cycles of violence and develop skills for sensitive, responsive parenting. PMEP includes a structured set of sessions, each 2 hours in duration: (1) becoming a group and safety planning, (2) identifying and understanding sources of stress, (3) strategies to build resilience and resolve conflict, (4) perinatal health and infant care, and (5) positive parenting.

For women randomized to receive RET, participation in the program will include five virtual RET sessions that aim to promote a positive, nurturing parent-child relationship during early childhood through training in sensitive parent-child communication about children's emotions. RET sessions will be 1 hour in duration. The program is manualized and each session includes teaching/review of skills, instructions/activity with rationale, reminiscing practice, and immediate video feedback by a family coach.

02

Conditions studied

  • Child Abuse
  • Intimate Partner Violence
  • Secondary Prevention
  • Parenting

Keywords

  • child abuse
  • child maltreatment
  • intimate partner violence
  • domestic violence
  • secondary prevention
  • parenting
03

In context

Lead sponsor

University of Notre Dame is the lead sponsor of 29 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
3 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

The sample will be composed of n=230 women and children drawn from an ongoing randomized clinical trial (RCT) of the PMEP (R01HD098092); during Year 1 of the current study, we will recruit an additional n=70 pregnant, IPV-exposed women and implement the PMEP RCT protocol with them, for a total sample of N=300 families.

In order to be eligible for the PMEP trial arm, women must be: 18 years or older, pregnant (between 10 and 30 weeks), English speaking, and exposed to IPV in the past year. To be eligible for re-enrollment in the RET trial arm, women must have previously participated in the PMEP trial arm. Women who have a significant mental health disorder or cognitive impairment that precludes their ability to understand or participate in the intervention will be excluded. Mothers who have experienced miscarriage, infant death, or who no longer have custody of the child with whom they were pregnant with when they participated in the PMEP trial arm will be excluded from the intervention given that the RET trial arm requires active participation from both parent and child; if, however, women have a child born after their participation in PMEP and who is in the study age range, they and their child may participate.

05

Study design

Phase
Phase 2
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
600 participants (estimated)

Study arms

  • Experimental
    PMEP + ECM

    In pregnancy: PMEP In early childhood: enhanced case management

    Behavioral: Pregnant Moms' Empowerment Program · Behavioral: Enhanced Case Management

  • Experimental
    Pregnancy - Active Control + RET

    In pregnancy: Women who are not randomized to PMEP participate in a contact-equivalent, non-directive social support group. In early-childhood: Women participant in the RET.

    Behavioral: Reminiscing and Emotion Training · Behavioral: Pregnancy - Active Control

  • Experimental
    PMEP + RET

    In pregnancy: PMEP In early childhood: Reminiscing and Emotion Training Program

    Behavioral: Pregnant Moms' Empowerment Program · Behavioral: Reminiscing and Emotion Training

  • Active comparator
    Pregnancy - Active Control + ECM

    In pregnancy: Women not randomized to PMEP will participate in a contact-equivalent, nondirective social support group. In early childhood: Families who are not randomized to the RET condition will be mailed a kit containing 5 packets to be opened weekly. Each packet includes a family activity and a newsletter with parenting materials.

    Behavioral: Pregnancy - Active Control · Behavioral: Enhanced Case Management

Interventions

  • BehavioralPregnant Moms' Empowerment Program

    Women who receive the PMEP complete a structured set of sessions delivered over the course of 5 weeks, each session lasts 2 hours in duration: (1) becoming a group \& safety planning, (2) identifying and understanding sources of stress, (3) strategies to build resilience and resolve conflict, (4) perinatal health and infant care, and (5) positive parenting.

    Also known as: PMEP

  • BehavioralReminiscing and Emotion Training

    Each of the 5 RET sessions are 1 hour in duration. The program is manualized and each session includes teaching/review of skills, instructions/activity with rationale, reminiscing practice, and immediate video feedback by a family coach.

  • BehavioralPregnancy - Active Control

    Women who are not randomized to the PMEP participate in a contact-equivalent, nondirective social support group.

    Also known as: AC

  • BehavioralEnhanced Case Management

    Families randomized to this attentional control condition will receive enhanced case management. They will be mailed a kit containing 5 packets to be opened weekly. Each packet includes a family activity and a newsletter with parenting materials (e.g., Adventures in Parenting curriculum developed by NICHD) that were selected to not overlap with RET content (e.g., reading together, fitness, etc.). Using mothers' responses regarding access to resources on the Family Resource Scale (Dunst \& Leet, 1987), which is completed during the baseline visit, mothers will also receive referrals to community resources for items rated as inadequate.

    Also known as: ECM

06

What researchers measure

Primary outcomes

  1. DCS Records - Maltreatment Classification System

    DCS records will be coded using the Maltreatment Classification System (MCS; Barnett et al., 1993). The MCS utilizes operational criteria for determining the occurrence of subtypes of maltreatment. Subtype categories include sexual abuse, physical abuse, physical neglect, and emotional maltreatment.

    Time frame: RET baseline (T5), 6 month follow-up (T8). 12 month follow-up

  2. Maternal Maltreatment Classification Interview

    MCS ratings will be supplemented by information obtained during the Maternal Maltreatment Classification Interview (MMCI; Cicchetti et al., 2002), a structured interview based on the MCS. It will be audiotaped and coded by two independent raters utilizing the same operational criteria as the MCS.

    Time frame: RET baseline (T5), 6 month follow-up (T8)

  3. Maltreatment risk/Propensity

    Mothers will complete the Child Abuse Potential Inventory (CAPI; Milner, 1986) and the Adult Adolescent Parenting Inventory (AAPI; Bavolek \& Keene, 2001), both of which assess maltreatment propensity. A composite variable of maltreatment propensity/risk will be created by combining these indicators.

    Time frame: PMEP baseline [T1], PMEP immediate post-test [T2], PMEP 3 month post-partum follow-up [T3], PMEP 12 month post-partum follow-up [T4], RET baseline [T5], RET immediate post-test [T6], RET 3 month follow-up [T7], RET 6 month follow-up [T8]

  4. Intimate partner violence

    others will complete the Revised Conflict Tactics Scale (CTS2) (Straus, Hamby, Boney-McCoy, \& Sugarman, 1996; Straus, 1979), which assesses the severity of psychological, physical, and sexual violence in a dating, cohabiting, or marital relationship. This measure has the advantage of being able to be flexibly coded to gain information about IPV severity, frequency, and chronicity.

    Time frame: PMEP baseline [T1], PMEP immediate post-test [T2], PMEP 3 month post-partum follow-up [T3], PMEP 12 month post-partum follow-up [T4], RET baseline [T5], RET immediate post-test [T6], RET 3 month follow-up [T7], RET 6 month follow-up [T8]

  5. Maternal Sensitivity - perinatal period

    Maternal sensitivity will be assessed in several observational contexts. At T3 and T4, mother-child dyads will participate in a 5-minute free play activity that will be coded using an established coding framework (Braungart-Rieker et al., 2014).

    Time frame: PMEP 3 month post-partum follow-up [T3], PMEP 12 month post-partum follow-up [T4]

  6. Maternal Sensitive Guidance - early childhood

    From T5-T8, maternal sensitive guidance will be assessed by following the Autobiographical Emotional Events Dialogue procedure (AEED; Koren-Kari e, Oppenheim, Haimovich, \& Etzion-Carasso, 2003b).

    Time frame: RET baseline [T5], RET immediate post-test [T6], RET 3 month follow-up [T7], RET 6 month follow-up [T8]

  7. Maternal Sensitivity - DPICS - early childhood

    Participants will also complete a 10-minute free play paradigm using an abbreviated Dyadic Parent-Child Interaction Coding System (DPICS; Eyeberg, et al., 2013). This free play will be coded for positive, neutral and negative patterns of parent-child communication.

    Time frame: RET baseline [T5], RET immediate post-test [T6], RET 3 month follow-up [T7], RET 6 month follow-up [T8]

Secondary outcomes

  1. Positive Parenting Behavior

    Positive parenting behavior will be assessed using selected subscales of the Alabama Parenting Questionnaire - Preschool Version (Clerkin, et al., 2007).

    Time frame: RET baseline (T5), RET immediate post-test (T6), 3 month follow-up (T7), 6 month follow-up (T8)

  2. Maternal emotional style

    Maternal emotion style will be assessed using the Maternal Emotional Style Questionnaire (Lagacé-Séguin' \& Coplan' 2005).

    Time frame: RET baseline (T5), RET immediate post-test (T6), 3 month follow-up (T7), 6 month follow-up (T8)

  3. Child Emotion Regulation

    Children's emotion regulation will be assess via parent report on the Emotion Regulation Checklist (Shields \& Cicchetti, 1997).

    Time frame: RET baseline (T5), RET immediate post-test (T6), 3 month follow-up (T7), 6 month follow-up (T8)

  4. Child Temperament - infancy

    Child temperament will be collected as a covariate. Mothers will complete the Infant Behavior Questionnaire at T4 (Rothbart, et al., 2001) which assesses multiple aspects of early child temperament.

    Time frame: PMEP 12 month postpartum follow-up (T4)

  5. Child Temperament - early childhood

    Child temperament will be collected as a covariate. Mothers will complete the the Child Behavior Questionnaire at T5-T8 (Rothbart, et al., 2001) which assesses multiple aspects of early child temperament.

    Time frame: RET baseline (T5), RET immediate post-test (T6), RET 3 month follow-up (T7), RET 6 month follow-up (T8)

  6. Child Adjustment

    Child adjustment will be assessed using the Child Behavior Checklist (Achenbach, 1999) at assessments T5-T8.

    Time frame: RET baseline (T5), RET immediate post-test (T6), RET 3 month follow-up (T7), RET 6 month follow-up (T8)

Other outcomes

  1. Maternal Trauma History

    Maternal exposure to lifetime trauma, including both interpersonal and non-interpersonal traumas, will be assessed using the Trauma History Questionnaire (Hooper et al., 2011) at baseline interviews \[T1, T5\].

    Time frame: PMEP baseline [T1], RET baseline [T5]

  2. Maternal Child Maltreatment History

    Women's history of child maltreatment, specifically, will be assessed using the Childhood Trauma Questionnaire (Berstein et al., 1997) at T5.

    Time frame: RET baseline [T5]

  3. Maternal Social Support

    Women's access to social supports (friends, family, neighborhood) will be assessed using the Lubben Social Network Scale (Lubben \& Gironda, 2004). This scale been used with IPV-exposed women.

    Time frame: PMEP baseline [T1], PMEP immediate post-test [T2], PMEP 3 month post-partum follow-up [T3], PMEP 12 month post-partum follow-up [T4], RET baseline [T5], RET immediate post-test [T6], RET 3 month follow-up [T7], RET 6 month follow-up [T8]

  4. Mother Verbal Ability

    RET is a verbally mediated intervention, so mother verbal ability will be included as a covariate in the analyses. Verbal ability will be assessed using the Peabody Picture Vocabulary Test - Fifth Edition (Dunn, 2018).

    Time frame: RET immediate follow-up [T6; mother]

  5. Maternal Mental Health - PTSD

    Maternal PTSD will be assessed using the PTSD Checklist-Civilian 5 (Weathers, et al., 2013).

    Time frame: PMEP baseline [T1], PMEP immediate post-test [T2], PMEP 3 month post-partum follow-up [T3], PMEP 12 month post-partum follow-up [T4], RET baseline [T5], RET immediate post-test [T6], RET 3 month follow-up [T7], RET 6 month follow-up [T8]

  6. Maternal Mental Health - Depression

    Maternal depression will be assessed using the Center for Epidemiological Studies Depression Scale (Radloff, 1977).

    Time frame: PMEP baseline [T1], PMEP immediate post-test [T2], PMEP 3 month post-partum follow-up [T3], PMEP 12 month post-partum follow-up [T4], RET baseline [T5], RET immediate post-test [T6], RET 3 month follow-up [T7], RET 6 month follow-up [T8]

  7. Child victimization

    This questionnaire is used in nationally representative surveillance studies (NatSCEV) and is a recommended tool for monitoring purposes relative to children's experiences of violence, in conjunction with formal, state-level data (Forston, et al., 2016). Children's exposure to other types of violence, outside of maltreatment (e.g., community violence) will be assessed using this tool.

    Time frame: RET baseline (T5), RET immediate post-test (T6), RET 3 month follow-up (T7), RET 6 month follow-up (T8)

  8. Child Verbal Ability

    RET is a verbally mediated intervention, so child verbal ability will be included as a covariate in the analyses. Verbal ability will be assessed using the Peabody Picture Vocabulary Test - Fifth Edition (Dunn, 2018).

    Time frame: RET baseline [T5] and RET 6 month follow-up [T8]

07

Study locations

2 sites
08

References and documents

Individual participant data

Plan to share: No — Participants were not consented for IPD sharing in the initial study. Study data are sensitive and some data is highly protected (e.g., DCS records).

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Nov 2024 (actual). Primary completion is estimated for Mar 2029, 52 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 4, 2024
First posted
Dec 13, 2024
StartActual
Nov 7, 2024
Primary completionEst.
Mar 30, 2029
CompletionEst.
Aug 31, 2029
Last update
Apr 23, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06732310
Lead sponsor
University of Notre Dame
Responsible party
Sponsor
First posted
Dec 13, 2024
Start date
Nov 7, 2024
Primary completion
Mar 30, 2029 (estimated)
Completion
Aug 31, 2029 (estimated)
Last update
Apr 23, 2026

Study contacts

Laura E Miller-Graff, PhD
principal investigator · University of Notre Dame
Kathryn H Howell, PhD
principal investigator · University of Wisconsin, Madison
Kristin Valentino, PhD
principal investigator · University of Notre Dame

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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