- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02225301
iLookOut for Child Abuse -Online Learning Module for Early Childcare Providers (iLookOut)
Early Childhood Practitioner's Knowledge and Attitudes Regarding Reporting Child Abuse/Neglect-iLookOut
Phase 1 was a randomized control trial that used a test-retest model to evaluate the impact of iLook Out for Child Abuse, an online, interactive learning module about reporting suspected child abuse. Delivered via a learning management system to early childhood professionals who work with infants and young children, this study assessed iLookOut's effect on 1) knowledge about reporting suspected child abuse; 2) attitudes toward reporting suspected child abuse; and 3) preparedness to protect children at risk.
Findings from Phase 1 were that iLookOut will improved knowledge, changed attitudes, and increase self-reported preparedness of early childhood providers to report suspected child abuse.
Phase 2 of this trial is an open-enrollment study that records pre-/post- data on the same measurements as Phase 1, and is available for use (free of charge) for all childcare providers in Pennsylvania at https://www.ilookoutforchildabuse.com.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Despite their daily interactions with young children, little research has been conducted into early childhood professionals' (ECPs') knowledge of, and attitudes towards, reporting of child abuse/neglect. This study:
- Evaluates the effectiveness of the online learning module, iLook Out for Child Abuse, created to train and inform early childhood providers about reporting suspected child abuse;
- Identifies early childhood providers' current knowledge regarding Pennsylvania law on mandated reporting of suspected child abuse;
- Explores the factors influencing early childhood providers' current knowledge and attitudes;
- Evaluates the impact of an online educational program on early childhood providers' knowledge, attitudes, and patterns of decision-making regarding mandated reporting of suspected child abuse;
- To explores the factors influencing the impact of an online educational program on early childhood providers' knowledge and attitudes regarding mandated reporting of suspected child abuse
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Nicole Verdiglione, BS
- Phone Number: 283-765 717-531-8521
- Email: nverdiglione@hmc.psu.edu
Study Contact Backup
- Name: Benjamin H Levi, MD PhD
- Phone Number: 717-531-8778
- Email: BHLevi@psu.edu
Study Locations
-
-
Pennsylvania
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Hershey, Pennsylvania, United States, 17033
- Recruiting
- Penn State Milton S. Hershey Medical Center / Penn State College of Medicine
-
Contact:
- Nicole Verdiglione, BA
- Phone Number: 283-765 717-531-8521
- Email: nverdiglione@pennstatehealth.psu.edu
-
Contact:
- Benjamin H Levi, MD PhD
- Phone Number: 717-531-8521
- Email: BHLevi@psu.edu
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Principal Investigator:
- Benjamin H Levi, MD PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Paid or volunteer staff at childcare facility
Exclusion Criteria:
- Younger than 18 years of age
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: iLook Out for Child Abuse
The online learning module is an interactive, multi-media, self-paced intervention.
|
The online learning module is an interactive, multi-media, self-paced intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in knowledge regarding reporting suspected child abuse.
Time Frame: 48 months
|
Participants will complete pre- and post-intervention measures regarding reporting suspected child abuse.
A sample of Phase 1 participants also repeated knowledge measures 3-6 months post-intervention.
|
48 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in attitudes regarding reporting suspected child abuse.
Time Frame: 48 months
|
Participants will complete pre- and post-intervention measures to assess attitudes regarding reporting suspected child abuse.
A sample of Phase 1 participants also repeated attitudinal measures 3-6 months post-intervention.
|
48 months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Evaluation of online learning module.
Time Frame: 48 months
|
Participants will complete a post-intervention questionnaire evaluating various aspects of the online learning module.
A sample of Phase 1 participants also repeated evaluation measures 3-6 months post-intervention.
|
48 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Benjamin H Levi, MD PhD, Penn State Milton S. Hershey Medical Center / Penn State College of Medicine
Publications and helpful links
General Publications
- Walsh K, Eggins E, Hine L, Mathews B, Kenny MC, Howard S, Ayling N, Dallaston E, Pink E, Vagenas D. Child protection training for professionals to improve reporting of child abuse and neglect. Cochrane Database Syst Rev. 2022 Jul 5;7(7):CD011775. doi: 10.1002/14651858.CD011775.pub2.
- Yang C, Panlilio C, Verdiglione N, Lehman EB, Hamm RM, Fiene R, Dore S, Bard DE, Grable B, Levi B. Generalizing findings from a randomized controlled trial to a real-world study of the iLookOut, an online education program to improve early childhood care and education providers' knowledge and attitudes about reporting child maltreatment. PLoS One. 2020 Jan 8;15(1):e0227398. doi: 10.1371/journal.pone.0227398. eCollection 2020.
- Mathews B, Yang C, Lehman EB, Mincemoyer C, Verdiglione N, Levi BH. Educating early childhood care and education providers to improve knowledge and attitudes about reporting child maltreatment: A randomized controlled trial. PLoS One. 2017 May 19;12(5):e0177777. doi: 10.1371/journal.pone.0177777. eCollection 2017.
Helpful Links
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 (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- IRB-1243
- IRB-0376 (Other Identifier: Penn State College of medicine)
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
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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