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Behavioral Intervention
READY To Stand Curriculum for Preventing Sexual Violence (Project LIVE Trial)
N/A
Recruiting
Led By Katie M Edwards, PhD
Research Sponsored by University of Nebraska Lincoln
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline and 1 month post rts delivery
Awards & highlights
Project LIVE Trial Summary
This trial will examine if a curriculum can help communities reduce violence, with the goal to spread it widely if it's successful.
Who is the study for?
This trial is for high school students in grades 9-12 at certain schools within the Des Moines Public School system who understand English. It's also for school staff over 18 years old working at these schools. Students not in specified grades or schools, and staff not meeting age/location criteria can't join.Check my eligibility
What is being tested?
The READY To Stand Curriculum aimed at preventing commercial sexual exploitation of children is being tested. The study will evaluate its effectiveness and potential for broader use if successful.See study design
What are the potential side effects?
Since this trial involves an educational curriculum, traditional medical side effects are not applicable. However, participants may experience emotional or psychological impacts from discussing sensitive topics.
Project LIVE Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline and 1 month post rts delivery
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline and 1 month post rts delivery
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Commercial sexual exploitation of children (CSEC) Victimization and Perpetration (STUDENT Reported)
Secondary outcome measures
Academic & Career Commitment (STUDENT Reported)
Alcohol Use (STUDENT Reported)
CSEC Bystander Opportunity and Action (STUDENT Reported)
+6 moreOther outcome measures
Bystander Readiness to Help (STUDENT Reported)
CSEC Bystander Intentions (SCHOOL PERSONNEL Reported)
CSEC Knowledge (SCHOOL PERSONNEL Reported)
+9 moreProject LIVE Trial Design
1Treatment groups
Experimental Treatment
Group I: RTS InterventionExperimental Treatment1 Intervention
RTS intervention will include a total of one 120-minute session of programming delivered to school personnel, and six, 45-minute sessions (total = 4.5 hours) for students. There are five components in this intervention that both students and school personnels will receive: 1) Psychoeducation on CSEC, 2) Healthy relationship skills training, 3) Programming components to enhance valuing of self and others, 4) Bystander intervention skills, and 5) Social norms for both students and school personnel. Students will additionally receive programming on Identification of safe people and resources, while school personnel will receive programming on Responding to Student Disclosures, and Cultural Humility.
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Who is running the clinical trial?
University of Nebraska LincolnLead Sponsor
34 Previous Clinical Trials
8,960 Total Patients Enrolled
The Set Me Free ProjectUNKNOWN
Centers for Disease Control and PreventionFED
875 Previous Clinical Trials
22,476,446 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am not in grades 9-12 or not enrolled in a DMPS high school.I am over 18 and work at one of the specified schools.I am over 18, work at a specified school, and am involved in teaching, administration, or support.
Research Study Groups:
This trial has the following groups:- Group 1: RTS Intervention
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is it possible for me to be included in this experiment?
"Potential participants must have experienced human trafficking and be between 10-25 years of age to join this clinical trial, which is enrolling up to 956 patients."
Answered by AI
Are there current opportunities to join this research trial?
"The clinical trial's information on clinicaltrials.gov suggests that it has closed enrollment since its initial post date of August 1st, 2023 and last update four days later. Despite this setback, 15 other studies have been made available to prospective participants as alternatives."
Answered by AI
Is the enrollment period for this research trial open to adults 18 and older?
"The requisite age range for this medical trial is between 10 and 25 years old. There are 8 sub-studies available to participants below the legal consenting age, while 4 studies specifically cater towards individuals aged 65 or older."
Answered by AI
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