- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06273618
iLookOut Micro-learning to Improve Knowledge Retention
iLookOut for Child Abuse: PA Microlearning to Improve Knowledge Retention
Study Overview
Status
Intervention / Treatment
Detailed 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.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Benjamin H Levi, MD PhD
- Phone Number: 717-531-8778
- Email: BHLEVI@psu.edu
Study Contact Backup
- Name: Nicole Verdiglione, MA
- Phone Number: 717-531-8778
- Email: nverdiglione@pennstatehealth.psu.edu
Study Locations
-
-
Pennsylvania
-
Hershey, Pennsylvania, United States, 17033
- Recruiting
- Penn State College of Medicine
-
Contact:
- Benjamin H Levi, MD, PhD
- Phone Number: 717-531-8778
- Email: BHLEVI@psu.edu
-
Contact:
- Nicole R Verdiglione, BA
- Phone Number: 283765 717-531-0003
- Email: nverdiglione@pennstatehealth.psu.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 18 years of age or older
Exclusion Criteria:
- Younger than 18 years of age
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Immediate
ECP participants who receive access to the Micro-Learning intervention immediately upon completing the Core Training.
|
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.
|
|
Active Comparator: 3-month
ECP participants who receive access to the Micro-Learning intervention 3 months after upon completing the Core Training.
|
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.
|
|
Active Comparator: 6-month
ECP participants who receive access to the Micro-Learning intervention 6 months after upon completing the Core Training.
|
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.
|
|
Active Comparator: 9-month
ECP participants who receive access to the Micro-Learning intervention 9 months after upon completing the Core Training.
|
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.
|
|
Active Comparator: Non-ECPs
Non-ECP participants
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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
|
3 months
|
|
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
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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
|
6 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- iLO-ML-23396
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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