iLook Out for Child Abuse: An Innovative Learning Module for Childcare Providers (iLookOut)

January 9, 2023 updated by: Benjamin H. Levi, Milton S. Hershey Medical Center
This five-year study aims to improve childcare provider (CCP) reporting of suspected child abuse by means of an online learning module, iLook Out for Child Abuse. Using an interactive, video-based story-line (along with follow-up activities), iLookOut engages CCPs emotionally and intellectually to take the first step in addressing the epidemic of child abuse -which in the U.S. claims >680,000 confirmed victims annually. The consequences of child abuse can be devastating and long-lasting. The purpose of this study is to establish an evidence-based intervention that can help those who care for young children recognize and report suspected child abuse before irreparable harm occurs.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This 5-year study will evaluate the efficacy of an innovative educational intervention, iLook Out for Child Abuse (iLookOut) for increasing rates of accurate child abuse reporting. Grounded in an Experiential Learning conceptual model, iLookOut is a multi-media, online intervention that engages learners emotionally and intellectually through an interactive, video-based story-line that provides education, challenges learners with decision-points, and gives critical feedback. iLookOut uses "gamification" strategies to promote experiential learning through simulation, problem-solving, and practice opportunities to apply new information and understanding. It also will include follow-up activities that promote retention and integration of new knowledge, as well as help CCPs to remain aware and engaged.

Prior studies have demonstrated that iLookOut significantly improves CCP knowledge and attitudes about reporting suspected child abuse, and is very well received by CCPs. To evaluate its impact on actual reporting behavior, the proposed research will randomize CCP sites in southern Maine (total = ~1,300) to receive iLookOut, Standard training, or Control (no intervention).

The primary goal is to increase the number of CCP reports for which either child abuse is confirmed or social services (e.g., therapeutic services, nutritional assistance) are recommended -as these are the kinds of reports that are likely to actually benefit a child.

The secondary goal is to decrease the proportion of reports that don't offer such benefit, and in particular to decrease costs to the state associated with intake and investigation of non-beneficial reports.

Study Type

Interventional

Enrollment (Actual)

2059

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

    • Pennsylvania
      • Hershey, Pennsylvania, United States, 17033
        • Penn State College of Medicine

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Works or volunteers at a childcare facility in Maine (i.e., home-based childcare, childcare center, Head Start facility, nursery school, pre-school)
  • 18 years of age or older

Exclusion Criteria:

  • Does not work or volunteer at a childcare facility in Maine
  • Under 18 years of age

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Sequential Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: iLookOut
Online, interactive learning program developed by study team.
Online, interactive educational intervention that uses a video-based story-line and "gamification" to teach childcare providers about child abuse and mandated reporting.
Other Names:
  • iLookOut
Active Comparator: Standard
Online mandated reporter training developed by the state of Maine during Y1, then recruited to complete iLookOut during Y2 and Y3.
Online, interactive educational intervention that uses a video-based story-line and "gamification" to teach childcare providers about child abuse and mandated reporting.
Other Names:
  • iLookOut
No Intervention: Control
No active recruitment or incentivizing of participants to complete any training on mandated reporting during Y1 and Y2, then recruited to complete iLookOut during Y3.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Percentage of "High Quality" reports of suspected child abuse submitted to the State of Maine by childcare providers
Time Frame: 48 months

Percentage of childcare provider reports (of suspected abuse) to the state of Maine that result in either i) child abuse being confirmed, or ii) social services being recommended for the child/family who was reported.

We will use Maine's Office of Child and Family Services' criteria for determining what counts as "confirmed child abuse" as well as what counts as a "recommended social service."

48 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Percentage of reports of suspected child abuse submitted to the State of Maine by childcare providers that are "Low Quality"
Time Frame: 48 months

"Low Quality" reports of suspected abuse are reports to the state of Maine that do not result in either findings of child abuse or recommended social services.

We will use Maine's Office of Child and Family Services' criteria for determining what counts as "confirmed child abuse" as well as what counts as a "recommended social service."

48 months
Financial costs (in U.S. dollars) associated with responding to "Low Quality" reports of suspected abuse that are submitted to the State of Maine by childcare providers
Time Frame: 48 months

Financial costs (in U.S. dollars) expended by the State of Maine on "Low Quality" reports (submitted by childcare providers during the study period) will be calculated by summing the following:

i) The average cost to the State of Maine associated with an "Intake call," multiplied by the number of reports of suspected abuse submitted by childcare providers that are screened out (i.e., determined by Intake workers to NOT warrant investigation); and

ii) The average cost to the State of Maine associated with investigating a report of suspected abuse, multiplied by the number of reports of suspected abuse submitted by childcare providers that are investigated, but NO abuse was confirmed AND no social services were recommended to the child/family that had been reported

48 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Benjamin H Levi, MD PhD, Penn State Milton S. Hershey Medical Center / Penn State College of Medicine

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

October 3, 2017

Primary Completion (Actual)

December 31, 2021

Study Completion (Actual)

February 1, 2022

Study Registration Dates

First Submitted

April 20, 2017

First Submitted That Met QC Criteria

June 9, 2017

First Posted (Actual)

June 14, 2017

Study Record Updates

Last Update Posted (Estimate)

January 11, 2023

Last Update Submitted That Met QC Criteria

January 9, 2023

Last Verified

January 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • IRB-4740
  • R01HD088448-01 (U.S. NIH Grant/Contract)

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

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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