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Behavioural Intervention

BASIS-T Strategy for Childhood Behavior Challenges (BASIS-T Trial)

N/A
Recruiting
Led By Aaron Lyon, PhD
Research Sponsored by University of Washington
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 beginning of school year, mid-school year, end of school year
Awards & highlights

BASIS-T Trial Summary

This trial will test a new strategy to help educators implement evidence-based practices to reduce social, emotional, and behavioral challenges in kids. This strategy focuses on motivating and influencing educators to help kids.

Who is the study for?
This trial is for K-5th grade teachers at elementary or K-8 schools who haven't been trained or supervised in Positive Greetings at the Door (PGD) in the past 5 years. Special education-only classroom teachers are not eligible.Check my eligibility
What is being tested?
The BASIS-T efficacy trial is testing a strategy called BASIS-T, designed to help teachers adopt and implement school-based practices to improve student social, emotional, and behavioral outcomes. It's compared with an Attention Control group.See study design
What are the potential side effects?
Since this trial involves educational strategies rather than medical interventions, it does not have side effects in the traditional sense. However, there may be varying impacts on teacher workload and stress.

BASIS-T Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~beginning of school year, mid-school year, end of school year
This trial's timeline: 3 weeks for screening, Varies for treatment, and beginning of school year, mid-school year, end of school year for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Implementation Outcome: Adoption
Implementation Outcome: Fidelity and Sustainment - Observed
Implementation Outcome: Fidelity and Sustainment - Self Report
+5 more
Secondary outcome measures
Student Behavioral Outcomes
Student Educational Outcomes

BASIS-T Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: BASIS-TExperimental Treatment1 Intervention
BASIS-T is designed to address the behavioral components often missing from standard EBPP training and consultation that relate to motivation prior to receiving EBPP training, and volition after EBPP training. It is an EBPP-agnostic implementation strategy designed to be delivered within the Preparation/Adoption phase, immediately prior to Active Implementation (CITE EPIS). BASIS-T targets behavioral intentions via improvement in attitudes, subjective norms, and self-efficacy.
Group II: Attention ControlPlacebo Group1 Intervention
Teachers assigned to the ACC will receive pre- and post-training experiences designed to mirror those received in the BASIS-T condition. These training experiences will be virtual, delivered by the same interventionist, and be approximately the same length as the BASIS-T experiences, but will not contain any of the BASIS-T content or mechanisms of change. The ACC pre-training experience will define, describe, and advocate for EBP implementation in schools. Content will be didactic, as is typical in professional development training for teachers.

Find a Location

Who is running the clinical trial?

Institute of Education SciencesFED
8 Previous Clinical Trials
2,936 Total Patients Enrolled
University of WashingtonLead Sponsor
1,741 Previous Clinical Trials
1,847,484 Total Patients Enrolled
Aaron Lyon, PhDPrincipal InvestigatorUniversity of Washington
3 Previous Clinical Trials
442 Total Patients Enrolled

Media Library

Attention Control (ACC) (Behavioural Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT05989568 — N/A
Childhood Behavior Research Study Groups: BASIS-T, Attention Control
Childhood Behavior Clinical Trial 2023: Attention Control (ACC) Highlights & Side Effects. Trial Name: NCT05989568 — N/A
Attention Control (ACC) (Behavioural Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05989568 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is there still space available for potential participants in this research project?

"Based on the data available from clinicaltrials.gov, this medical trial is still actively searching for participants. The original posting date was September 1st 2021 and it has been edited as recently as August 9th 2023."

Answered by AI

How many participants are currently eligible for this clinical research?

"Affirmative. Clinicaltrials.gov's records show that this research project, originally posted on September 1st 2021, is still recruiting participants for its experimental trials. The study requires 276 individuals to be recruited from a single designated medical centre."

Answered by AI
~184 spots leftby Jul 2026