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NCT Number: NCT06273618

iLookOut Micro-learning to Improve Knowledge Retention

This project investigates whether a multi-faceted strategy involving iLookOut's evidence-based Core Training plus an innovative follow-up Micro-Learning can promote knowledge retention and change behavior among early childhood professionals (ECPs) with regard to child abuse and its reporting. Additionally, this study will evaluate if non-ECPs experience similar improvements and retention of knowledge and changes in behavior as do ECPs.

Recruiting

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

The primary purpose of this study is to understand the optimal timing to administer iLookOut Micro-Learning to boost ECPs waning knowledge and preparedness to protect children from abuse. Additionally, this study will conduct a randomized controlled trial to examine how interactive, gamified micro-learning promotes knowledge retention and fosters behavior change with regard to child abuse and its reporting, and to establish that implementation of this intervention is feasible.

All components of the learning module being studied are online, and will be accessed by participants through a secure website.

Once they complete the Core Training, participants who identify as ECPs will receive an email indicating which randomization arm they are in (regarding access to the advanced training) - immediate, 3 months, 6 months, or 9 months. Non-ECPs will be able to complete the advanced training as soon as they complete the Core Training. All non-ECPs will be used as a comparison group to determine if the iLookOut trainings are effective for improving and retaining knowledge, and changing behavior among Non-ECPs compared to the ECP participants.

Separate mixed-effects linear regression model will be applied to assess (1) the knowledge decay effect based on the data collected at different time-points and (2) the behavior change between the various time-points and how it is correlated to the knowledge score, after controlling for participants' baseline characteristics and work setting. In addition, the regression model will adjust effects for allocation blocks and the factors for stratification in the analysis to reduce group variability.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years of age or older

Exclusion criteria

  • Younger than 18 years of age

Treatment and study plan

Micro-Learning

Other

Micro-Learning involves a series of 5-10 minute interactive, gamified learning exercises delivered to smart-phones (or computers) to reinforce and augment knowledge and promote attitudes and behavior to promote children's wellbeing.

Primary outcomes

  1. Change in knowledge about child maltreatment and its reporting as assessed by validated iLookOut knowledge test

    Time frame: 3 months

    Validated knowledge test regarding child maltreatment and its reporting

  2. Change in behavior regarding child maltreatment and its reporting as measured by self-report questionnaire

    Time frame: 3 months

    Self-report questionnaire of behavior regarding child maltreatment and its reporting

Secondary outcomes

  1. Comparison of early childhood professionals vs. non-early childhood professionals

    Time frame: 6 months

    Comparison knowledge and behavioral outcomes for early childhood professionals vs. non-early childhood professionals

Study contacts

Contact information is provided by the study sponsor or research team.

Benjamin H Levi, MD PhD

CONTACT

[email protected]

717-531-8778

Nicole Verdiglione, MA

CONTACT

[email protected]

717-531-8778

Sponsors and collaborators

Lead sponsor

Milton S. Hershey Medical Center

Other

Registry information

Official study title

iLookOut for Child Abuse: PA Microlearning to Improve Knowledge Retention

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Feb 22, 2024
Registry last updated
Aug 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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