- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07526142
Evaluation of Circles of Safety
April 7, 2026 updated by: Center for Violence Prevention Research Inc
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
- Name: Melissa Bright
- Phone Number: 904-728-1020
- Email: mbright@scienceofviolence.org
Study Locations
-
-
Florida
-
Gainesville, Florida, United States, 32609
- Recruiting
- Center for Violence Prevention Research
-
Contact:
- Melissa Bright, PhD
- Phone Number: 9047281020
- Email: mbright@scienceofviolence.org
-
-
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.
Clinical Trials on Child Abuse Sexual
-
Oral Health Centre of Expertise in Western NorwayEducational storytelling forlag og filmCompletedChild Abuse | Oral Health | Child Neglect | Child Maltreatment | Child Sexual Abuse | Dental NeglectNorway
-
Johns Hopkins Bloomberg School of Public HealthUniversity of Massachusetts, Lowell; Barry UniversityCompletedChild Sexual Abuse | Program Evaluation | Perpetration of Child Sexual Abuse | Prevention InterventionUnited States
-
New York UniversityTerminatedChild Sexual AbuseUnited States
-
Northeastern UniversityEnrolling by invitation
-
Penn State UniversityCompleted
-
Anne Revah-LevyRecruitingChild Sexual AbuseFrance
-
New York UniversityRecruitingChild Sexual AbuseUnited States
-
University of MinnesotaCompleted
-
The New York Society for the Prevention of Cruelty...National Institutes of Health (NIH)CompletedSafe Touches: A Rigorous Evaluation of a Sexual Abuse Prevention Program for Children (Safe Touches)Child Sexual AbuseUnited States
Clinical Trials on Circles of Safety
-
Simon Fraser UniversityCanadian Institutes of Health Research (CIHR)Completed
-
Colorado School of Public HealthUniversity of Colorado, Denver; CU Thrive: Office for Well-being | Center for...Not yet recruitingBurnout | Leadership | Professional Fulfillment | Belonging | Intent to LeaveUnited States
-
Texas Woman's UniversityCompletedParent SupportUnited States
-
Réseau de soins DeltaCompletedDeprescription | Benzodiazepine (BZD) and Related DrugsSwitzerland
-
University of California, San FranciscoNational Institutes of Health (NIH); Oregon Health and Science University; My...CompletedMental Health Wellness 1 | Health Care Utilization | Financial Hardship | Education, ProfessionalUnited States
-
Cedars-Sinai Medical CenterStryker NordicCompletedTibial Fractures | Nonunion of Fracture | Femur Fracture | Tibia Fracture | Nonunion of Fracture of Tibia | Nonunion of Fracture of Femur (Diagnosis)United States
-
Milton S. Hershey Medical CenterNational Institute of Nursing Research (NINR)Not yet recruitingGamification | Advance Care Planning | American Indian or Alaska Native
-
University GhentUniversity Hospital, Ghent; AZ Sint-Jan AV; Algemeen Ziekenhuis Maria Middelares and other collaboratorsCompletedHealthy Volunteers | Aortic Aneurysm, AbdominalBelgium
-
MU-JHU CAREJohns Hopkins UniversityCompleted
-
University of Massachusetts, WorcesterNational Institute on Alcohol Abuse and Alcoholism (NIAAA)RecruitingPTSD | Alcohol; Use, ProblemUnited States