- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05572398
Online Bullying Bystander Intervention for Middle Schools Phase II (STACII)
February 19, 2026 updated by: Klein Buendel, Inc.
Translating an In-Person Brief, Bystander Bullying Intervention (STAC) to a Technology-Based - Phase II
School interventions to reduce bullying can be effective but also require substantial time and resources.
Online technologies have the potential to deliver effective bullying interventions to a large number of middle school students for less cost.
The feasibility of delivering the effective STAC bullying intervention through a mobile web app will be tested using focus groups with middle school students and development and usability testing and the efficacy of the program will be tested using a randomized controlled trial.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
While studies support the efficacy of comprehensive, school-wide interventions in reducing bullying, these types of programs can require significant time and financial resources for implementation, resulting in barriers to providing school-based bullying prevention, especially in low-income and rural communities.
Additionally, although training bystanders to act as "defenders" on behalf of targets of bullying is an important intervention component, few programs include this as part of their comprehensive strategy.
Brief programs that focus on bystander training and require fewer resources are needed to reduce bullying and its negative consequences.
The PI (Dr.
Midgett) developed STAC, a brief, stand-alone bullying bystander intervention for middle school students, to reduce bullying and mental health risks for bystanders.
Brief, in-person programs, however, still pose implementation barrier such as training school personnel, providing external support, and not allowing for large groups of students to be trained at the same time.
For this project, the investigators propose to develop a technology-based STAC intervention (STAC-T) that will allow students to customize their experience by selecting avatars and bullying scenarios based on our previous studies conducted in a range of middle schools, including those in low-income and rural communities.
The investigators will also incorporate an assessment and personalized feedback component to promote behavior change.
The innovative, user-centered design proposed will be inherently sensitive to cultural needs of students and identify personally-appropriate strategies.
The specific aims of this application include building the program leveraging our prior work and expertise of an external advisory board, usability and effectiveness testing with middle school students and stakeholders to evaluate feasibility, and testing the efficacy of the program with a randomized controlled trial.
The technology-based platform will increase the overall reach, impact, and sustainability of the STAC intervention for bullying prevention.
It will substantially reduce cost to increase reach and its interactivity and algorithms can tailor program content to adapt it further for students attending low-income and rural schools.
Thus, this low-cost, easy to disseminate technology-based bullying bystander intervention has the potential to have a substantial impact on the problem of bullying and the negative associated consequences for both students who are targets and bystanders in middle school when the problem of bullying peaks.
There is a large market for the STAC-T intervention with approximately 100,000 public and private schools with middle-school grades in the United States.
Globally, the online education market is growing at 10% a year and the digital health market exceeds $220 billion annually.
Study Type
Interventional
Enrollment (Actual)
613
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 Locations
-
-
Idaho
-
Boise, Idaho, United States, 83725-1135
- Boise State University
-
-
Mississippi
-
University, Mississippi, United States, 38677-1848
- University of Mississippi
-
-
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
11 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria for Students:
- being enrolled in grades 6, 7, or 8 in a middle/junior high school in Idaho, Oregon, Mississippi, or New Hampshire.
- being selected by school counselors and teachers for having a desire to make a positive difference at school, be mature, and have the ability to positively engage with peers and adults (Aims 1 and 2).
- speaks and reads English or Spanish.
- parent consents and student assents for participation.
Exclusion Criteria for Students:
- participated in a previous study on STAC.
- speaks and reads only a language other than English or Spanish.
- does not consent and/or assent for participation.
Inclusion Criteria for School Personnel:
- employed in a middle/junior high school in Idaho or Mississippi with grades 6, 7, or 8.
- employed as a principal, teacher, or school counselor.
- speaks and reads English or Spanish.
- consents to participate.
Exclusion Criteria for School Personnel:
- participated in a previous study on STAC.
- speaks and reads only a language other than English or Spanish.
- does not consent for participation.
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: STAC-T
STAC-T is a brief technology-based bullying bystander intervention using four strategies: "Stealing the show," "Turning it over," "Accompanying others," and "Coaching compassion."
The online curriculum is delivered to middle-school students.
|
Middle school participants will complete online modules to learn about anti-bullying techniques and bystander intervention.
|
|
No Intervention: Assessment Only Control
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Student-Advocates Pre- and Post-Scale (SAPPS)
Time Frame: Baseline assessment, 30-day assessment
|
An 11 item questionnaire measuring students' knowledge of buying, knowledge of the STAC-T strategies, and students' confidence to intervene in bullying situations.
Items are rated on a 4-point Likert Scale ranging from 1 (Totally Disagree) to 4 (Totally Agree) and were summed to compute a total scale score.
The minimum value is 11 and the maximum value is 44, and a higher score means a better outcome.
|
Baseline assessment, 30-day assessment
|
|
Bullying and Cyberbullying Scale for Adolescents (BCS-A) - Victimization Scale at 30 Days
Time Frame: Baseline assessment, 30-day assessment
|
This questionnaire measures bullying and cyberbullying victimization in the past 30 days.
The 13-item Victimization Scale assesses in-person bullying victimization with 8 items and cyberbullying victimization with 5 items.
Items are rated on a 5-point Likert Scale ranging from 0 (Never) to 4 (Four or More Times) and were summed to compute a total scale score.
The minimum value is 0 and the maximum value is 52, and a higher score means a worse outcome.
|
Baseline assessment, 30-day assessment
|
|
Use of Strategies at 30 Days Post-intervention
Time Frame: 30-day assessment
|
Questions rating the student's use of each STAC-T strategy using a single item rated on a 5-point Likert scale: "How often would you say you have used these strategies to stop bullying in the past month?"
(a) Stealing the Show; (b) Turning it Over; (c) Accompanying Others; and (d) Coaching Compassion.
Total strategies reflects the number of students who used at least one of the four STAC-T strategies.
Results are reported for students who reported witnessing bullying in the past 30-days (n=125/229).
|
30-day assessment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Center for Epidemiological Studies Depression Scale for Children
Time Frame: Baseline assessment, 6-week assessment
|
The 20-item CES-DC measures depressive symptoms in children on a four-point Likert Scale.
The minimum value is 0 and the maximum value is 60, and a higher score means a worse outcome.
|
Baseline assessment, 6-week assessment
|
|
The Social Avoidance and Distress Scale - General and Fear of Negative Evaluation Scale in the condition Social Anxiety Scale for Adolescents (SAS-A)
Time Frame: Baseline assessment, 6-week assessment
|
The 18-item Social Avoidance and Distress Scale - General and Fear of Negative Evaluation Scale will measure anxiety.
The minimum value is 0 and the maximum value is 72, and a higher score means a worse outcome.
|
Baseline assessment, 6-week assessment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Mary Buller, MA, Klein Buendel, Inc.
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)
May 26, 2022
Primary Completion (Actual)
November 18, 2024
Study Completion (Actual)
November 18, 2024
Study Registration Dates
First Submitted
September 20, 2022
First Submitted That Met QC Criteria
October 6, 2022
First Posted (Actual)
October 7, 2022
Study Record Updates
Last Update Posted (Actual)
February 24, 2026
Last Update Submitted That Met QC Criteria
February 19, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0337
- 5R42MD014943 (U.S. NIH Grant/Contract)
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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