Clinical Trials Directory

Trials / Terminated

TerminatedNCT06195852

Maximizing the Reach of Universal Child Sexual Abuse Prevention: An Equivalence Trial

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
26 (actual)
Sponsor
New York University · Academic / Other
Sex
All
Age
7 Years – 10 Years
Healthy volunteers
Accepted

Summary

The goal of this clinical trial is to test the equivalence of two delivery modalities of a universal child sexual abuse prevention program, Safe Touches: usual vs. modified. The aims are to: 1. Determine the equivalence of effectiveness between usual and modified Safe Touches 2. Assess the maintenance of gains between usual and modified Safe Touches 3. Examine factors that may impact the future dissemination and implementation

Detailed description

Child sexual abuse (CSA) is a public health problem affecting 1 in 5 girls and 1 in 12 boys before age 18. National estimates indicate children ages 7 to 13 are at highest risk for CSA and CSA is associated with lifelong negative sequelae. School-based prevention programs offer cost-effective universal programming teaching students an array of personal safety skills. Several programs have demonstrated effectiveness in increasing children's knowledge of self-protection, and some have been linked with facilitating disclosures, including Safe Touches. Effectiveness notwithstanding, the programmatic reach of universal school-based programs is limited by the inherent reliance on school infrastructure and a dearth of available alternative delivery modalities. The current study is designed to address this gap by leveraging an existing partnership between university-based researchers (NYU), the Safe Touches model developer (NYSPCC), and community-based organizations with active implementations of Safe Touches. The study will use a rigorous cluster randomized design to determine the equivalence of effectiveness between two delivery modalities of Safe Touches: as usual vs. modified. The usual workshop will be delivered by two facilitators with live puppet skits, as designed (N=90). Whereas, the modified workshop will be delivered by one facilitator utilizing pre recorded skit videos (N=90). The research team will determine the equivalence of concept learning acquisition (Aim 1) and retention (Aim 2) among students in classrooms that receive the as usual or modified workshop. To conclude equivalence, it is important to examine factors that may impact future dissemination and implementation, specifically program adoption among school personnel and implementation fidelity (Aim 3). Study findings will inform the ongoing development of effective CSA prevention programs and policy decisions regarding the sustainable integration of such programs within schools. Given the scope and burden of CSA, especially among elementary aged students, it is a public health priority to efficiently disseminate effective school-based prevention programs on a wide scale.

Conditions

Interventions

TypeNameDescription
BEHAVIORALUsual Safe TouchesThe in-person Safe Touches workshop is delivered in the classroom by 2 facilitators with live puppet skits, as designed.
BEHAVIORALModified Safe TouchesThe modified Safe Touches workshop will be delivered by 1 facilitator in the classroom by utilizing prerecorded workshop skit videos.

Timeline

Start date
2024-09-01
Primary completion
2025-04-21
Completion
2025-04-21
First posted
2024-01-08
Last updated
2025-04-29

Locations

4 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT06195852. Inclusion in this directory is not an endorsement.