Actively Recruiting
Systematic Efficacy Replication Study of Conjoint Behavioral Consultation in Elementary Schools
Led by American Institutes for Research · Updated on 2023-02-09
720
Participants Needed
1
Research Sites
192 weeks
Total Duration
On this page
Sponsors
A
American Institutes for Research
Lead Sponsor
W
Wisconsin Center for Education Research
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this project is to conduct an impact evaluation of the Conjoint Behavioral Consulting (CBC) intervention under real-world conditions as an IES Efficacy Replication trial. CBC is a family-school partnership intervention proven efficacious for children with serious emotional and behavior problems. The investigation will conduct a systematic efficacy replication of CBC to identify important process and context variables in need of attention prior to a CBC effectiveness study. School-based specialists (SBSs) will implement CBC and will be responsible for working directly with parents and teachers who have a student with or at risk for severe emotional disturbance, with more implementation support (i.e., non-routine conditions) than would be expected under routine conditions to ensure adequate fidelity of implementation. The research questions examine the impact of CBC, when implemented by SBSs, on student, parent, and teacher outcomes, as well its effect on mediational pathways. In addition, the research team will gather stakeholder feedback in focus groups to provide information about factors that stakeholders perceive as impeding or promoting CBC adoption, implementation, and sustainability.
CONDITIONS
Official Title
Systematic Efficacy Replication Study of Conjoint Behavioral Consultation in Elementary Schools
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Enrolled in kindergarten, Grade 1, Grade 2, Grade 3, or Grade 4 at recruitment
- Among the 12 students with the highest risk score on the Behavioral and Emotional Screening System 3 Behavioral and Emotional Screening System (BASC3-BESS) in the above grade span in their school (among those with parental consent for screening).
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Trial Site Locations
Total: 1 location
1
Madison Metropolitan School District
Madison, Wisconsin, United States, 53703
Actively Recruiting
Research Team
E
Elizabeth Spier, PhD
CONTACT
Y
Yibing Li, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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