Training of Mental Health ProfessionalsTraining of Frontline Health Workers
Investigational drug(s) / intervention(s)
MBPS App
MBPS App: A MBPS web application designed and built on a customizable case management platform (CommCare) to support non-specialist providers will be used by study participants for approximately 3 months.
Study summary
The goal of this project is to enhance and evaluate the efficacy of a scalable digital solution designed to help train and support the work of non-specialist providers (NSPs), such as community health workers, to deliver therapy to individuals with anxiety and/or depression. The main questions this project aims to answer are:
* Can a digital tool help NSPs feel more confident in counseling patients?
* How can a digital tool be designed to optimally support the work of NSPs?
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
* 18 years of age or older;
* English-speaking; and
* Completed EMPOWER Behavioral Activation training
Exclusion Criteria:
\- Unable to participate in virtual meetings
Primary outcome measure(s)
Change in Behavioral Activation (BA) Quality over Sessions — 12 weeks, from enrollment to study completion (assessed every 4 weeks) The BA Quality Scale for Healthy Activity Program score will be used to assess differences in BA quality over 3 sessions as scored by self and peer based on review of recordings. The BA Quality Scale ranges from 0 to 8, with higher scores indicating higher quality.
Change in Self-Efficacy — 12 weeks, from enrollment to study completion (assessed at Baseline and Endline) The Counselor Self-Efficacy Scale (SE-12) will be used to assess change in self-efficacy before and after the intervention. The scale ranges from 0 to 120 with higher scores indicating higher self-efficacy.
Trial sites (1)
Facility
City
Region
Status
Baylor Scott & White Health
Dallas
Texas
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
We use cookies to analyse site traffic and improve your experience. With your consent, we may also use cookies for advertising. You can change your choice at any time.