The Impact of Mechanisms of Action in Unguided Digital Mental Health Interventions
1 other identifier
interventional
172
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2024
1 active site
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
CompletedFirst Posted
Study publicly available on registry
July 23, 2024
CompletedStudy Start
First participant enrolled
September 15, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
October 30, 2025
CompletedFebruary 24, 2026
February 1, 2026
1.1 years
July 11, 2024
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 COMPARATORThis is the standard intervention arm
DPT-TP
EXPERIMENTALThis is the enhanced intervention arm
Interventions
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.
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.
Eligibility Criteria
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
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.
PMID: 40397492DERIVED
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