- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05661864
Multi-Tiered Systems of Support for Teacher Training in Classroom Management
February 8, 2023 updated by: Western Kentucky University
Multi-Tiered Systems of Teacher Training and Classroom Management
The goal of this clinical trial is to test the effects of a responsive approach to training teachers to increase their use of evidence-based classroom management practices.
The main question to answer is whether teachers increase their use of a target classroom management practice when they receive the intervention.
All participants will receive the intervention.
The target practice for which they receive intervention will be randomly assigned.
Participants will submit videos of an instructional activity in their classroom 1-2 times per week over a period of 12-15 weeks.
They will be asked to complete online modules on classroom management practices and to self-monitor their use of one classroom management practice.
Participants may also be asked to graph their data, watch videos of themselves teaching, or implement peer coaching with a classmate or other participant.
Researchers will compare the change in target classroom management practices between groups to test if the change in the group who targeted the practice is greater than the change in the group who did not target the practice.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
70
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
-
-
Kentucky
-
Bowling Green, Kentucky, United States, 42101
- Recruiting
- Western Kentucky University
-
-
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
- CHILD
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Enrolled in EDU 502 or PK-12 classroom teacher
Exclusion Criteria:
- Inability to submit video recordings of instruction for data collection and analysis
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: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Multi-Tiered Systems of Support for Teacher Training Evaluation
Participants will be randomized to a target practice group.
The group will receive the multi-tiered systems of support (online instruction, self-monitoring, self-management) for the target practice.
They will not receive instruction on the non-target practice until after study data collection concludes.
|
In tier 1 of the intervention, all participants will complete online modules on the target practice and self-monitoring.
They will then self-monitor the target practice for approximately three weeks.
Non-responders will receive intensified intervention (tier 2) in which they will complete an online module on self-management.
They will then self-manage their use of the target practice for approximately 3 weeks.
Continued non-responders will receive peer coaching on the target practice (tier 3).
Responders to tiers 2-3 will move down a tier after 3 weeks of response.
|
|
NO_INTERVENTION: Control
Participants will not receive intervention on the non-target practice until after study data collection concludes.
This practice will serve as the comparison for the group who received intervention on the practice.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in the frequency of the target practice
Time Frame: Baseline, endpoint (15 weeks from start date)
|
The investigators will measure the frequency of the target practice during baseline and treatment sessions.
|
Baseline, endpoint (15 weeks from start date)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
August 22, 2022
Primary Completion (ANTICIPATED)
May 1, 2023
Study Completion (ANTICIPATED)
May 1, 2023
Study Registration Dates
First Submitted
December 14, 2022
First Submitted That Met QC Criteria
December 14, 2022
First Posted (ACTUAL)
December 22, 2022
Study Record Updates
Last Update Posted (ACTUAL)
February 10, 2023
Last Update Submitted That Met QC Criteria
February 8, 2023
Last Verified
February 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 1950299-1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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