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Middle School Teacher Module for a Brief Bullying Intervention Program
N/A
Waitlist Available
Research Sponsored by Boise State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediate post-training (50 minutes)
Awards & highlights
No Placebo-Only Group
Summary
This study evaluates the feasibility and short-term outcomes of a teacher training designed as a companion module to a bullying bystander intervention (STAC) for middle school students in rural communities. The aim of this project is to provide a brief, low-cost intervention that can be easily disseminated as part of a school-based bullying prevention program to address this important public health problem.
Eligible Conditions
- Bullying
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ immediate post-training (50 minutes)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~immediate post-training (50 minutes)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Bullying Self-Efficacy
Comfort Managing Bullying
Confidence Managing Bullying
+2 moreSecondary study objectives
Number of Participants Reporting a Score of 3 or 4 on Acceptability and Relevance of the Teacher STAC Training
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: STAC Teacher ModuleExperimental Treatment1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
STAC Teacher Module
2022
N/A
~20
Find a Location
Who is running the clinical trial?
Boise State UniversityLead Sponsor
12 Previous Clinical Trials
6,502 Total Patients Enrolled
3 Trials studying Bullying
1,015 Patients Enrolled for Bullying
Mental Research InstituteUNKNOWN
1 Previous Clinical Trials
16 Total Patients Enrolled