NCT05229146

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
48

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jun 2022

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 18, 2022

Completed
21 days until next milestone

First Posted

Study publicly available on registry

February 8, 2022

Completed
4 months until next milestone

Study Start

First participant enrolled

June 2, 2022

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 21, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 21, 2023

Completed
1.3 years until next milestone

Results Posted

Study results publicly available

March 14, 2025

Completed
Last Updated

March 14, 2025

Status Verified

February 1, 2025

Enrollment Period

1.5 years

First QC Date

January 18, 2022

Results QC Date

November 18, 2024

Last Update Submit

February 22, 2025

Conditions

Keywords

episodic future thinkingdelay discountingparent-child relationslow incomesubstance use treatmentpeer recovery coach

Outcome Measures

Primary Outcomes (2)

  • Change in Monetary Choice Questionnaire

    The brief Monetary Choice Questionnaire (MCQ) is a 21-item binary-choice task that 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). "Larger later" amounts are separated into small, medium and large magnitudes. For the purposes of this study, to limit participant burden, we administered only small and large magnitude subscales, resulting in a total number of 14 items. The measure is scored to derive a single "total score" discounting rate k, with larger values reflecting greater preference for smaller sooner reward. Because k distributions are typically skewed, post-hoc natural logarithmic transformations were performed, resulting in normal distributions; thus, there is no maximum and minimum value. The MCQ has been shown to have strong psychometric properties among adults and correlates with real rewards, as well as real-world risk behaviors.

    Baseline, 1 week, 4 weeks

  • Change in Consideration of Future Consequences Scale-Parenting Score

    The Consideration of Future Consequences Scale-Parenting Adapted (CFCS-14-PA) is a 14-item self-report questionnaire composed of two subscales reflecting either immediate or future orientation related to parents interactions with their children. Items range from "not at all like me" (1) to "very much like me" (5) and are summed to create future or immediate orientation subscale, each composed of 7 items with score ranges from 7-35. Lower scores on the future orientation and higher scores on the immediate orientation subscales are associated with less future orientation and predictive of less engagement in health behaviors. The measure has been used extensively among adult samples and demonstrates strong reliability and validity. Change in CFCS-14-PA score is measured by comparing scores at the post-intervention assessment (approximately 4 weeks after baseline) with baseline scores.

    Baseline, 4 weeks

Secondary Outcomes (4)

  • Change in Dyadic Parent-Child Interaction Coding System Scores

    Baseline, 4 weeks

  • Change in Alabama Parenting Questionnaire Score

    Baseline, 4 weeks

  • Change in Emotion Regulation Checklist

    Baseline, 4 weeks

  • Client Satisfaction Questionnaire

    4 weeks

Study Arms (1)

Episodic Future Thinking

EXPERIMENTAL

Mothers will receive episodic future thinking (EFT). Mothers will meet with a "peer mother" who will administer the EFT intervention, including generation of several specific future events reflecting positive interactions with their child. We will also teach each parent a behavioral parent training element called Special Play Time. Following this session, mothers will receive daily text messages over the course of two weeks including a reminder cue generated as part of the EFT and a prompt to remember these episodes in vivid detail.

Behavioral: Episodic Future Thinking

Interventions

Episodic future thinking (EFT) includes a focus on generating detailed and vivid descriptions of future events. For the current intervention, EFT will be modified to have mothers describe specific events with their children.

Episodic Future Thinking

Eligibility Criteria

Sexfemale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Be the mother from the Flint area of a child between the ages of 5-10 who can provide legal consent for that child to participate in this study
  • Self-report that the child lives with them for at least 50% of the time
  • 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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

RL Jones Community Outreach Center

Flint, Michigan, 48505, United States

Location

Results Point of Contact

Title
Dr. Julia Felton
Organization
Henry Ford Health

Publication Agreements

PI is Sponsor Employee
No
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Scientist

Study Record Dates

First Submitted

January 18, 2022

First Posted

February 8, 2022

Study Start

June 2, 2022

Primary Completion

November 21, 2023

Study Completion

November 21, 2023

Last Updated

March 14, 2025

Results First Posted

March 14, 2025

Record last verified: 2025-02

Locations