Evaluation of Circles of Safety

Evaluation of Circles of Safety for the Primary Prevention of Child Sexual Abuse

Using a matched cluster randomized control design, the proposed study will evaluate a child sexual abuse (CSA) primary prevention strategy, Circles of Safety®. League leadership, staff, and coaches within youth sports will be focal participants. Outcomes include CSA among youth athletes served, protective and inappropriate behaviors from coaches & league leaders, as well as knowledge of and perceived ability to identify and address CSA and resource-seeking behavior.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

1500

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 Contact

Study Locations

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Participants must be at least 18 years of age.
  • Participants must be a youth sports leader or coach.
  • Participants must be an English speaker.
  • Participants must be able to provide consent for themselves.

Exclusion Criteria:

  • Children are not included as direct participants in this study.
  • Anyone who is not able to provide consent because they are a non-English speaker or have cognitive impairment.

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Complete Circles of Safety Training Program
participants will be asked to complete the Circles of Safety training program
The Circles of Safety program is a child sexual abuse (CSA) primary prevention program that provides direct education to organization leaders and adults who interact with youth, tailored website content for organizations that serve youth, and helpline services for all individuals affected by CSA including not only victims and their families but also individuals who think they may have or will sexually abuse a child.
No Intervention: Control
participants will not be asked to complete the Circles of Safety training program

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Rates of disclosed child sexual abuse
Time Frame: This will be measured at baseline and T2 (baseline + 90 days)
This will be measured at baseline and T2 (baseline + 90 days)
Rates of potentially harmful sexual behaviors from coaches and staff
Time Frame: This will be measured at baseline and T2 (baseline + 90 days)
This will be measured at baseline and T2 (baseline + 90 days)
Staff and coaches' knowledge of CSA
Time Frame: This will be measured at baseline and T2 (baseline + 90 days)
This will be measured at baseline and T2 (baseline + 90 days)
Staff and coaches perceived self-efficacy in identifying CSA
Time Frame: This will be measured at baseline and T2 (baseline + 90 days)
This will be measured at baseline and T2 (baseline + 90 days)
Rates of preventive behaviors among staff and coaches
Time Frame: This will be measured at baseline and T2 (baseline + 90 days)
This will be measured at baseline and T2 (baseline + 90 days)

Secondary Outcome Measures

Outcome Measure
Time Frame
Program reach
Time Frame: Measured through study completion, an average 1 year
Measured through study completion, an average 1 year
implementation consistency
Time Frame: Measured through study completion, an average 1 year
Measured through study completion, an average 1 year
mechanisms of intervention success
Time Frame: Measured through study completion, an average 1 year
Measured through study completion, an average 1 year

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Melissa Bright, PhD, Center for Violence Prevention Research

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)

April 1, 2025

Primary Completion (Estimated)

June 1, 2027

Study Completion (Estimated)

September 30, 2027

Study Registration Dates

First Submitted

February 19, 2026

First Submitted That Met QC Criteria

April 7, 2026

First Posted (Actual)

April 13, 2026

Study Record Updates

Last Update Posted (Actual)

April 13, 2026

Last Update Submitted That Met QC Criteria

April 7, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • CE22-003
  • U01CE003409 (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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