- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05539170
Parents' Differential Susceptibility to Microtrial
August 11, 2025 updated by: Rabia Chhangur, Tilburg University
Parents' Differential Susceptibility to a Randomized Controlled Microtrial: The Role of Physiological Signals as Underlying Mechanism
This randomized controlled microtrial, not just focus on parental (and child) responsiveness but also on an underlying physiological mechanism hypothesized to contribute to heightened susceptibility to parenting interventions.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
After being informed about the study, all participants giving written informed consent will be randomly assigned to the "micro" intervention condition (i.e., immediate positive parenting feedback) or care-as-usual control condition in a singe-blind manner in a 1:1 ratio.
Study Type
Interventional
Enrollment (Actual)
101
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Tilburg, Netherlands, 5037 AB
- Tilburg School of Social and Behavioral Sciences
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Parents with children aged 4-6 years.
Exclusion Criteria:
- psychiatric/neurological disorder (as reported by the parent)
- mental retardation (IQ < 70)
- not mastering the Dutch language, and
- that their child is not living in another household during the weekdays
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: "micro" parenting intervention
Parents will be instructed to bring the completed questionnaires with them to the university lab.
Then, in the lab, parents will be observed interacting with their child.
Following these baseline conditions, half of the parents will receive the "micro" parenting intervention-in the form of individual positive feedback concerning their parenting and their child's behavior.
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Individual positive feedback concerning their parenting and their child's behavior.
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No Intervention: care-as-usual condition
Participants in the care-as-usual control condition receive no immediate positive parenting feedback but will also be taken aside without their child, receiving only the instructions of the experiment.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parental self-efficacy beliefs assessed with the General Scale of Parental Self-Efficacy Beliefs (GSPSEB) at pretest, posttest and follow-up
Time Frame: Parenting change: baseline (pretest), after 2 weeks (posttest), and after 4 weeks (follow-up)
|
This 25-item scale is related to five domain-specific SEB factors: Discipline, Nurturance, Playing, Instrumental Care, and Teaching.
Self-efficacy beliefs in parenting can be evaluated as a quantitative construct by asking parents their beliefs in specific parenting activities, such as teaching, playing, providing instrumental care, nurturing or disciplining their child.
Items are in the form of affirmatives, for example: ''I am able to sense when my child is starting to become distressed'' for the Nurturance subscale.
The items will be rated on a 5-point scale (1 = strongly disagree to 5 = strongly agree).
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Parenting change: baseline (pretest), after 2 weeks (posttest), and after 4 weeks (follow-up)
|
|
Parenting behavior assessed with the short version of the Parental Behavior Scale (PBS-S) at pretest, posttest and follow-up
Time Frame: Parenting change: baseline (pretest), after 2 weeks (posttest), and after 4 weeks (follow-up)
|
This questionnaire consists of 25 items and comprises five subscales: Positive parenting (e.g., "I make time to listen to my child, when he/she wants to tell me something"), Discipline (e.g., "When my child has been disobedient, I give him/her a chore as punishment"), Harsh Punishment (e.g., "I spank my child when he/she is disobedient or naughty"), Material Rewarding (e.g., "I give my child candy as a reward for good behavior"), and Rule Setting (e.g., "I teach my child to be polite at school").
A 5-point scale is provided for each item, ranging from 1 = (almost) never to 5 = (almost) always.
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Parenting change: baseline (pretest), after 2 weeks (posttest), and after 4 weeks (follow-up)
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Observed parenting behavior assessed with the Crowell Parent-Child interaction taks at pretest and posttest
Time Frame: Parenting change: baseline/pretest observation at lab (before intervention) and posttest observation at same labvisit (after intervention)
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The Crowell observation task takes 20 minutes to complete and consists of four episodes: warm-up, free play, frustration task, and recovery time.
The parent scales (i.e., positive affect, autonomy support, negative affect, withdrawal, controlling behavior and laxness/inconsistent) are each internally consistent and well-defined conceptually.
High internal consistency for each scale provides support for the reliability of the rating scale, and suggests that the Crowell scores can be useful as scale to measure caregiver responsiveness, but also collectively as a total score assessing overall relational functioning.
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Parenting change: baseline/pretest observation at lab (before intervention) and posttest observation at same labvisit (after intervention)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child externalizing problem assessed with the Eyberg Child Behavior Inventory (ECBI) at pretest, posttest and follow-up.
Time Frame: Change in child behavior: baseline (pretest), after 2 weeks (posttest), and after 4 weeks (follow-up)
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One subscale assessing the degree to which child externalizing problem is a problem from the 36-item Eyberg Child Behavior Inventory (ECBI) will be used to assess the occurrence of child externalizing problem behavior.
This "Intensity" subscale measures frequency of externalizing behavior in children aged 2 to 16 years and has been shown to be a reliable (screening) instrument (3).
Example items are: "Does not obey house rules" and "Whines."
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Change in child behavior: baseline (pretest), after 2 weeks (posttest), and after 4 weeks (follow-up)
|
|
Observed child behavior assessed with the Crowell Parent-Child interaction taks at pretest and posttest
Time Frame: Change in child behavior: baseline/pretest observation at lab (before intervention) and posttest observation at same labvisit (after intervention)
|
The Crowell observation task takes 20 minutes to complete and consists of four episodes: warm-up, free play, frustration task, and recovery time.
The child scales (i.e., positive affect, persistence/enthusiasms, irritability/negative affect, and noncompliance) are each internally consistent and well-defined conceptually.
High internal consistency for each scale provides support for the reliability of the rating scale, and suggests that the Crowell scores can be useful as scale to measure child's affective presentation, but also collectively as a total score assessing overall relational functioning.
|
Change in child behavior: baseline/pretest observation at lab (before intervention) and posttest observation at same labvisit (after intervention)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Rabia R. Chhangur, PhD, Tilburg University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 1, 2022
Primary Completion (Actual)
February 14, 2025
Study Completion (Actual)
February 14, 2025
Study Registration Dates
First Submitted
September 6, 2022
First Submitted That Met QC Criteria
September 9, 2022
First Posted (Actual)
September 14, 2022
Study Record Updates
Last Update Posted (Actual)
August 14, 2025
Last Update Submitted That Met QC Criteria
August 11, 2025
Last Verified
April 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- TSB_RP604
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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