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NCT Number: NCT06145919

Parent-Child Memory Study: Improving Future Thinking Among Mothers

Parents of children from impoverished communities are disproportionately more likely to engage in harsh physical discipline, which can lead to serious clinical outcomes, including suicidal ideation and attempts. One mechanism linking low resource environments and maladaptive parenting strategies is maternal delay discounting, or the tendency to value smaller, immediate rewards (such as stopping children's misbehavior via physical means) relative to larger, but delayed rewards (like improving the parent-child relationship). This study will examine the efficacy of implementing a low-cost, brief intervention targeting the reduction of maternal delay discounting to inform broader public health efforts aimed at improving adolescent mental health outcomes in traditionally underserved communities.

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Key information

Age range

5 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Mothers of Joy Institute for Parenting and Family Wellness, Inc

Flint, Michigan, 48503, United States

Location status: Recruiting

Location contact

Shearese Stapleton

CONTACT

About this study

Harsh parenting is associated with serious and costly mental health problems among youth, including substance use, mood disorders, and suicidal ideation and behaviors. Of concern, these parenting practices are most common among families from impoverished communities; however, many behaviorally-based parenting interventions do not take into account the unique mechanisms linking environmental disadvantage to parenting approaches. While the causes of harsh parenting are complex and varied, one such mechanism may be parents' tendencies to prioritize immediate rewards (such as stopping a child's misbehavior via physical punishment like spanking and hitting) relative to larger, but delayed rewards (including improved parent-child relationship quality), known as delay discounting.

The aims of the current study are to conduct a Stage 1 parent-child dyad randomized control trial (RCT) (n = 72) examining the effectiveness of a brief, episodic future thinking (EFT) intervention in a community setting serving low-income mothers and additional implementation data. Participants will be randomized to receive either Episodic Future Thinking (EFT) or Episodic Recent Thinking (ERT) intervention arms. This case series will examine the efficacy of episodic future thinking (EFT) compared to episodic recent thinking (ERT) to target reduction of parenting-related delay discounting. Outcomes will evaluate the effect of EFT on reducing maternal delay discounting and harsh parenting and improving child clinical outcomes.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Parent Inclusion Criteria:

  • A mother and or grandmother from the Flint area with a child/grandchild between the ages of 5-10 who can provide legal consent for that child
  • Self-report that they have consistent contact with the child/grandchild
  • Willing to participate in the study
  • Able to participate in written assessments and an intervention conducted in English
  • Have a working cell phone that can receive and send text messages and be willing to receive/send text messages as part of the study
  • Have a phone or device that's able to use video conferencing software if interested in virtual participation

Parent Exclusion Criteria:

  • Self-disclosed active suicidality/homicidality
  • Self-disclosed current bipolar disorder, schizophrenia, or psychosis
  • Self-reported current and ongoing involvement with child protective services

Child Inclusion Criteria:

  • Children must be between the ages of 5-10 and have a mother/grandmother willing to provide consent for their participation
  • Willing to participate in parent-child observation sessions
  • Elementary proficiency in English
  • Willing to participate in study surveys

Child Exclusion criteria:

  • Self-disclosed active suicidality/homicidality
  • Self-disclosed current bipolar disorder, schizophrenia, or psychosis

Treatment and study plan

Episodic Future Thinking (EFT)

Behavioral

The adapted episodic future thinking (EFT) intervention will focus on generation of vivid, substance-free, rewarding events that could happen in the future with their children.

Episodic Recent Thinking (ERT)

Behavioral

In the episodic recent thinking (ERT) condition, the participant will instead describe in vivid details events that have occurred in the recent past.

Primary outcomes

  1. Change in Monetary Choice Questionnaire

    Time frame: Baseline, Intervention, Week 2, Month 3, Month 6, Month 9

    The Monetary Choice Questionnaire (MCQ) is a 27-item binary-choice task, which asks participants to select between two hypothetical monetary amounts: a smaller reward available immediately (e.g. $49 today) or a larger reward available after a delay (e.g. $60 in 89 days). The measure is scored to derive a discounting rate k, with larger values reflecting more problematic rates of discounting. Because k distributions are typically skewed, post-hoc natural logarithmic transformations will be performed, which have been shown to approximate normal distributions. The MCQ has been shown to have strong psychometric properties among adults and correlates with real rewards, as well as real-world risk behaviors.

  2. Change in Consideration of Future Consequences Scale Score

    Time frame: Baseline, Intervention, Week 2, Month 3, Month 6, Month 9

    The Consideration of Future Consequences Scale1 (CFCS-14) is a 14-item self-report questionnaire that assesses active consideration of longer-term implications of an individual's actions. Lower scores on the CFCS-14 are associated with a greater focus on immediate needs and have been found to be associated with less engagement in health behaviors1819 and greater substance use. The measure has been used extensively among adult samples and demonstrates strong reliability and validity. Research suggests modest but significant correlations with the MCQ. Change in CFCS-14 score is measured by comparing scores at the post-intervention assessment timepoints with baseline scores.

Secondary outcomes

  1. Change in Alabama Parenting Questionnaire Score

    Time frame: Baseline, Intervention, Week 2, Month 3, Month 6, Month 9

    Parents will report on their parenting styles and behavior using the Alabama Parenting Questionnaire (APQ). The APQ consists of five subscales that yield two broadband "positive" and "negative" parenting factors. The measure is widely used and validated among parenting populations. 42 items are ranked on a scale of 1-5 and scores are computed for each subscale (with possible scores ranging from 3-15 for corporal punishment to 10-50 for longer subscales including parental monitoring and involvement). Higher scores reflect greater levels of each subscore domain.

  2. Change in Emotion Regulation Checklist

    Time frame: Baseline, Intervention, Week 2, Month 3, Month 6, Month 9

    Parents will report on children's emotion regulation using the Emotion Regulation Checklist (ECR). The ECR includes 24 items that yield two subscales: (1) lability/negativity and (2) emotion regulation. The measure is widely used and validated for parent-report of older children and young adolescents.

Study contacts

Contact information is provided by the study sponsor or research team.

Julia Felton, PhD

CONTACT

[email protected]

704-995-7832

Sponsors and collaborators

Lead sponsor

Henry Ford Health System

Other

Collaborators

  • Michigan State University
  • University of Kansas
  • University of Maryland, College Park

Registry information

Official study title

Parent-Child Memory Study: Improving Future Thinking Among Mothers From a Traditionally Underserved Community to Reduce Harsh Parenting and Improve Child Outcomes - A Randomized Controlled Trial

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Nov 24, 2023
Registry last updated
May 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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