ClinicalTrials.Veeva

Menu

iLookOut Micro-learning to Improve Knowledge Retention

Penn State Health logo

Penn State Health

Status

Enrolling

Conditions

Knowledge
Practice
Attitudes

Treatments

Other: Micro-Learning

Study type

Interventional

Funder types

Other

Identifiers

NCT06273618
iLO-ML-23396

Details and patient eligibility

About

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.

Full description

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.

Enrollment

12,000 estimated patients

Sex

All

Ages

18 to 100 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18 years of age or older

Exclusion criteria

  • Younger than 18 years of age

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

12,000 participants in 5 patient groups

Immediate
Active Comparator group
Description:
ECP participants who receive access to the Micro-Learning intervention immediately upon completing the Core Training.
Treatment:
Other: Micro-Learning
3-month
Active Comparator group
Description:
ECP participants who receive access to the Micro-Learning intervention 3 months after upon completing the Core Training.
Treatment:
Other: Micro-Learning
6-month
Active Comparator group
Description:
ECP participants who receive access to the Micro-Learning intervention 6 months after upon completing the Core Training.
Treatment:
Other: Micro-Learning
9-month
Active Comparator group
Description:
ECP participants who receive access to the Micro-Learning intervention 9 months after upon completing the Core Training.
Treatment:
Other: Micro-Learning
Non-ECPs
Active Comparator group
Description:
Non-ECP participants
Treatment:
Other: Micro-Learning

Trial contacts and locations

1

Loading...

Central trial contact

Benjamin H Levi, MD PhD; Nicole Verdiglione, MA

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems