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Strengthening Child Social-Emotional and Lifestyle Health in Families Experiencing Stress

Strengthening Child Social-Emotional Functioning and Healthy Lifestyle Behaviors Through Parent-Based Prevention in Families Experiencing Major Stressors

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06163703
Enrollment
86
Registered
2023-12-11
Start date
2024-02-09
Completion date
2026-05-07
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Child Behavior, Parenting, Sedentary Behavior, Self-regulation

Brief summary

This study evaluates feasibility and preliminary efficacy of a parent-based prevention program to promote social-emotional and lifestyle behavior health among 3- to 9-year-old children in families experiencing major stressors.

Detailed description

Social-emotional difficulties and unhealthy lifestyle behaviors are prevalent among children in the U.S. and are associated with negative health outcomes. These challenges are even more pronounced among families who deal with major stressors, such as parental trauma history and mental health difficulties, parental chronic illness (e.g., HIV), parental substance use, economic disadvantage, and racial discrimination. The purpose of this study is to assess the feasibility, acceptability, and preliminary efficacy of a parent-based preventive intervention targeting parental self-regulation, stress reduction, and positive parenting, to promote child social-emotional and lifestyle behavior health, among families where the parents (a) have a child aged 3 to 9 years old, (b) have concerns about their child's behavior, mood, and/or lifestyle health, and (c) are experiencing major stressors. The intervention to be tested is based on Family Life Skills Triple P.

Interventions

BEHAVIORALFamily Life Skills Triple P

The intervention is a 12-session program that combines parenting support with trauma-informed life skills coaching. It includes content related to positive parenting strategies, self-regulation, coping with emotions, effective communication, dealing with the past, and developing healthy habits.

Sponsors

University of South Carolina
Lead SponsorOTHER
National Institute of General Medical Sciences (NIGMS)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
3 Years to 9 Years
Healthy volunteers
Yes

Inclusion criteria

1. Child between the ages of 3-9 years 2. Parent/caregiver willing to engage in the intervention who * is at least 18 years of age * is primary caregiver or guardian for the participating child * has concerns about the child's mood, behavior, and/or lifestyle health * is experiencing two or more major stressors of the following: trauma history, mental health difficulties, living with HIV, racial discrimination, substance misuse, and/or financial strain * is English speaking.

Exclusion criteria

a. Parent or child has * a significant cognitive disability, developmental delay, or pervasive developmental disorder * active suicidal or homicidal ideation * psychotic symptoms (active hallucinations, delusions, or impaired thought processes) * ongoing family violence occurring within the home and/or active involvement of child protect services related to child maltreatment allegations.

Design outcomes

Primary

MeasureTime frameDescription
Intervention acceptabilitypost-intervention (T2, Weeks 16-18)Assessed as parent-reported liking and approval of the intervention on a 5-point response scale and satisfaction with the intervention on a 4-point response scale, with higher scores indicating greater acceptability.
Intervention appropriatenesspost-intervention (T2, Weeks 16-18)Assessed as parent-reported applicability and suitability of the intervention on a 5-point response scale, with higher scores indicating greater appropriateness.
Intervention feasibility--Implementabilitypost-intervention (T2, Weeks 16-18)Assessed as parent-reported ease of use and overall implementability of the intervention on a 5-point response scale, with higher scores indicating greater feasibility.
Intervention feasibility--AttendanceWeekly throughout intervention period (Weeks 1-17)Assessed as parent attendance at intervention sessions using weekly attendance logs
Trial-related feasibility--Recruitment capabilityContinuously throughout recruitment period, up to 156 weeksAssessed as the proportion of eligible children who enroll in the study.
Trial-related feasibility--RetentionContinuously through study period (Weeks 1-30)Assessed as the proportion of enrolled children who remain in the study through the length of the intervention, with proportion who dropout and reasons for dropout also collected.
Child social-emotional difficulties: Problem behaviorsbaseline (T1, Weeks 0-2); post-intervention (T2, Weeks 16-18); follow-up (T3, Week 30)Assessed as parent-reported frequency of child problematic behaviors on a 7-point response scale (higher scores indicate greater frequency).
Child social-emotional difficulties: Depression and anxiety symptomsbaseline (T1, Weeks 0-2); post-intervention (T2, Weeks 16-18); follow-up (T3, Week 30)Assessed as parent-reported frequency of child depression and anxiety symptoms on a 4-point response scale (higher scores indicate greater frequency).
Child social-emotional difficulties: Strengths and difficultiesbaseline (T1, Weeks 0-2); post-intervention (T2, Weeks 16-18); follow-up (T3, Week 30)Assessed as parent-reported agreement with statements about child strengths and difficulties on a 3-point response scale (higher scores indicate greater endorsement).
Child physical activitybaseline (T1, Weeks 0-2); post-intervention (T2, Weeks 16-18); follow-up (T3, Week 30)Assessed as daily time spent sedentary and in various activity intensities using a wrist-worn accelerometer.
Child screen timebaseline (T1, Weeks 0-2); post-intervention (T2, Weeks 16-18); follow-up (T3, Week 30)Assessed as parent-reported average daily time spent engaging in screen time, including: watching TV; using a computer; gaming on a console or hand-held device; and using a tablet or smart phone for activities such as viewing videos, playing games, and browsing the internet.
Child sleepbaseline (T1, Weeks 0-2); post-intervention (T2, Weeks 16-18); follow-up (T3, Week 30)Assessed using a wrist-worn accelerometer to calculate nighttime sleep duration and using a validated measure of parent-reported child sleep-wake behaviors on a 6-point response scale, with lower scores indicating more problematic behaviors.

Secondary

MeasureTime frameDescription
Parenting practicesbaseline (T1, Weeks 0-2); post-intervention (T2, Weeks 16-18); follow-up (T3, Week 30)Assessed as parent self-reported frequency of positive and negative parenting behaviors on a 5-point response scale, with higher subscale scores indicating greater frequency of the respective behaviors.
Parenting self-regulationbaseline (T1, Weeks 0-2); post-intervention (T2, Weeks 16-18); follow-up (T3, Week 30)Assessed as parent self-rated agreement with statements about self-regulation as a parent on a 7-point response scale, with higher scores indicating greater self-regulation.
Parenting stressbaseline (T1, Weeks 0-2); post-intervention (T2, Weeks 16-18); follow-up (T3, Week 30)Assessed as parent self-rated frequency and intensity of daily parenting hassles on a 4--point response scale, with higher scores indicating more frequent and intense hassles.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORNada M Goodrum, Ph.D.

University of South Carolina

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 2, 2026