- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03791281
Beliefs and Attitudes for Successful Implementation in Schools (BASIS)
December 29, 2018 updated by: Aaron Lyon, University of Washington
The goal of this study is to adapt and test the feasibility and potential efficacy of a theory-driven pre-implementation intervention to address individual-level barriers to EBP implementation - Beliefs and Attitudes for Successful Implementation in Schools (BASIS) - designed to improve school mental health providers' implementation of EBPs.
BASIS is intended to be a feasible and scalable first-line or adjunctive implementation enhancement intervention that is facilitative of other efforts (e.g., organizational interventions) that target high quality EBP implementation.
Aims of this study are to: (1) Adapt an existing, theory-driven implementation intervention (BASIS), previously used with educators, to improve the EBP implementation behaviors of school mental health providers; and (2) Assess the viability of a later clinical trial by: (a) establishing the feasibility, acceptability, and appropriateness of the BASIS intervention among school mental health providers, and (b) Pilot testing BASIS, as compared to an Attention Control, delivered as pre-implementation intervention prior to training in a specific, existing EBP.
Key organizational factors (e.g., implementation climate) will also be evaluated and included as covariates and we will explore trends in the data to inform the design of a larger trial.
Ultimately, BASIS offers an innovative and scalable approach to improving school mental health providers' uptake and use of EBPs in order to increase the number of youth with mental health problems who receive high quality services.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
35
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
-
-
Washington
-
Seattle, Washington, United States, 98115-8160
- University of Washington School Mental Health Assessment, Research, and Training (SMART) Center
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion:
School mental health providers (school psychologists, school social workers, etc.) recruited from middle and high schools in two economically and ethnically diverse districts in the Seattle area.
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: BASIS
Received a 3-hour BASIS implementation strategy.
|
|
Active Comparator: Attention Control
Received a 3-hour session designed to control for dose, information provided, and presenter effects.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Attitudes toward Evidence-Based Practices
Time Frame: Pre-intervention/baseline, post-intervention (1-2 weeks), 4-month follow-up
|
Evidence-Based Practice Attitudes Scale (EBPAS) is a widely used 26-item tool designed to assess evidence-based practice (EBP) attitudes with items measured on a 0-4 scale and 6 subscales: (1) likelihood of adopting if the EBP were a requirement; (2) likelihood of adopting if the EBP were appealing to you; (3) openness to new practices; (4) perceived divergence between current practices and EBPs; (5) fit of EBPs with current practices; and (6) burden of EBPs.
Subscale and total scores are mean scores of items with a range of 0-4.
Higher scores reflect more favorable attitudes (perceived divergence is reverse-coded).
|
Pre-intervention/baseline, post-intervention (1-2 weeks), 4-month follow-up
|
Change in Subjective Norms
Time Frame: Pre-intervention/baseline, post-intervention (1-2 weeks), 4-month follow-up
|
Subjective Norms Scale is based on Theory of Planned Behavior (TPB) constructs.
Two subscales measure two types implementation-related subjective norms: injunctive norms and descriptive norms.
Four items load on each subscale and mean score range from -3 to +3, with positive scores reflecting more positive subjective injunctive and descriptive norms.
|
Pre-intervention/baseline, post-intervention (1-2 weeks), 4-month follow-up
|
Change in Perceived Behavioral Control
Time Frame: Pre-intervention/baseline, post-intervention (1-2 weeks), 4-month follow-up
|
Perceived Behavioral Control Scale is a modified version of the Teacher's Self-Efficacy Scale, which has 10 items assessing perceived behavioral control in implementing evidence-based practices.
Items are scored on a 1-4 scale with a total mean score ranging from 1-4.
Higher scores reflect greater (i.e., more favorable) perceived behavioral control.
|
Pre-intervention/baseline, post-intervention (1-2 weeks), 4-month follow-up
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in School Implementation Citizenship Behaviors
Time Frame: Pre-intervention/baseline, post-intervention (1-2 weeks), 4-month follow-up
|
The School Implementation Citizenship Behaviors Scale (S-ICBS) includes 15 items and measures clinicians' perceptions of how school staff engage with evidence-based practices in their specific school context.
There are 4 subscales: (1) helping others; (2) keeping informed; (3) taking initiative; and (4) advocacy.
Subscale and total scores are mean scores of items with a range of 0-4.
Higher scores reflect greater (i.e., more favorable) implementation citizenship behavior.
|
Pre-intervention/baseline, post-intervention (1-2 weeks), 4-month follow-up
|
Change in Intentions to Implement
Time Frame: Pre-intervention/baseline, post-intervention (1-2 weeks), 4-month follow-up
|
The Modified Intentions to Use Scale has 9 items assessing school mental health providers' intentions to implement evidence-based practices.
A total mean score is computed with a range of 0-4 and higher scores indicate more favorable intentions.
Two versions of this scale were administered.
At baseline, all providers were asked about general intentions to implement evidence-based practices.
After training, clinicians were asked about intentions to implement the specific intervention for which they had received training.
|
Pre-intervention/baseline, post-intervention (1-2 weeks), 4-month follow-up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Aaron R Lyon, PhD, University of Washington
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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 15, 2016
Primary Completion (Actual)
July 31, 2018
Study Completion (Actual)
July 31, 2018
Study Registration Dates
First Submitted
December 21, 2018
First Submitted That Met QC Criteria
December 29, 2018
First Posted (Actual)
January 2, 2019
Study Record Updates
Last Update Posted (Actual)
January 2, 2019
Last Update Submitted That Met QC Criteria
December 29, 2018
Last Verified
December 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- 52139
- 1R21MH108714 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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