NCT06514326

Brief Summary

This randomized controlled trial (RCT) will compare two interventions that utilize the same evidence-based components of established digital parent training programs (DPTs) aimed at treating child behavior problems, but that differ in terms of the quality of therapeutic persuasiveness (TP) quality (standard: DPT-STD; enhanced TP: DPT-TP). The investigators will recruit parents from 160 families with 3-7-year-old children with behavior problems who will be randomized into one of the two intervention arms. The investigators will measure child behavior problems and related parenting variables before, during, and after the intervention. DPT usage will be passively collected. The investigators hypothesize that, compared to DPT-STD, parents allocated to the DPT-TP arm will have significantly better module completion rates (adherence to the program) and report better outcomes - measured by improvements in child behavior problems and related parenting variables. The investigators also hypothesize that changes in reported outcomes will be mediated by module completion rates. Therefore, comparing two active interventions that only differ in terms of their TP quality will enable to examine the causal link between this conceptual mechanism of action and beneficial outcomes.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
172

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2024

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

July 11, 2024

Completed
12 days until next milestone

First Posted

Study publicly available on registry

July 23, 2024

Completed
2 months until next milestone

Study Start

First participant enrolled

September 15, 2024

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 30, 2025

Completed
Last Updated

February 24, 2026

Status Verified

February 1, 2026

Enrollment Period

1.1 years

First QC Date

July 11, 2024

Last Update Submit

February 23, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Eyberg Child Behavior Inventory (ECBI)

    Child behavior problems will be assessed using the Intensity subscale of the 36-item ECBI. For each item, caregivers rate the intensity of the behavior (1 = never to 7 = always).

    From baseline to 6 months follow-up

Secondary Outcomes (7)

  • The Parenting Scale (PS)

    From baseline to 6 months follow-up

  • Alabama Parenting Questionnaire (APQ)

    From baseline to 6 months follow-up

  • The Parenting Tasks Checklist (PTC)

    From baseline to 6 months follow-up

  • Parental Self Efficacy (Me as a Parent [MaaP])

    From baseline to 6 months follow-up

  • Specific Parenting Practices (SPP)

    From baseline to 6 months follow-up

  • +2 more secondary outcomes

Other Outcomes (4)

  • Minutes of use-Program usage

    From baseline to 10 weeks time

  • Number of logins-Program usage

    From baseline to 10 weeks time

  • Unique days-Program usage

    From baseline to 10 weeks time

  • +1 more other outcomes

Study Arms (2)

DPT-STD

ACTIVE COMPARATOR

This is the standard intervention arm

Behavioral: DPT-STD

DPT-TP

EXPERIMENTAL

This is the enhanced intervention arm

Behavioral: DPT-TP

Interventions

DPT-TPBEHAVIORAL

This intervention includes all the ingredients of DPT-STD, but with additional features that correspond to the conceptual model of therapeutic persuasiveness. Each theme in the program comprises a learning phase followed by a 1-2 week focusing phase. Accordingly, the program utilizes the following features: 1. Call to action: Parents receive timely triggers via text messages that are related to the specific goals and therapeutic activities of the modules they have completed. 2. Monitoring and ongoing feedback of user state: Specific practices currently taught are documented within the system through a brief daily report, on which parents receive feedback. 3. Adaptation to user state: Parents' reports on their activities are used to acknowledge their success and to suggest additional actions based on the specific goals reported by parents. Effort related to desired therapeutic activities is adapted based on graded tasks.

DPT-TP
DPT-STDBEHAVIORAL

This intervention is similar in its features to other programs that deliver DPT, and is suitable for use on computers or on mobile devices. An icon is positioned on the mobile device home screen in order to enable quick access to the program. The DPT-STD comprises seven 10- to 25-minute modules, each corresponding to one of the themes mentioned above. Each module's content includes videos and texts guiding the parent through the training process, and interactive features, such as multiple-choice questions with direct feedback. Additional features embedded within the platform include downloadable materials and a "questions and answers" section that contains frequently asked questions.

DPT-STD

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Parents having a child between the ages of 3 and 7
  • The parents report high levels of behavior problems demonstrated by their child based on the ECBI Intensity subscale (X ≥ 132)
  • The parents have access to a smartphone device with an Internet connection.

You may not qualify if:

  • The child is taking medication for behavioral or emotional problems
  • The child is in regular contact with a professional for behavioral or emotional problems
  • their child has been diagnosed with an intellectual disability or developmental delay
  • The parents are currently accessing parenting support elsewhere

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Haifa

Haifa, Israel, 3498838, Israel

Location

Related Publications (1)

  • Baumel A, Aderka IM. The Impact of Mechanisms of Action on Adherence and Outcomes in Self-Guided Digital Mental Health Interventions: Protocol for a Randomized Controlled Trial With Mediation Analysis. JMIR Res Protoc. 2025 May 21;14:e71238. doi: 10.2196/71238.

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

July 11, 2024

First Posted

July 23, 2024

Study Start

September 15, 2024

Primary Completion

October 30, 2025

Study Completion

October 30, 2025

Last Updated

February 24, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

Locations