NCT07082010

Brief 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?

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
55

participants targeted

Target at P25-P50 for not_applicable

Timeline
3mo left

Started May 2025

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress81%
May 2025Aug 2026

First Submitted

Initial submission to the registry

May 14, 2025

Completed
1 day until next milestone

Study Start

First participant enrolled

May 15, 2025

Completed
2 months until next milestone

First Posted

Study publicly available on registry

July 24, 2025

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Last Updated

April 20, 2026

Status Verified

April 1, 2026

Enrollment Period

1.1 years

First QC Date

May 14, 2025

Last Update Submit

April 15, 2026

Conditions

Keywords

anxietydepressionbehavioral activationtask-sharingcommunity health workersdigital health

Outcome Measures

Primary Outcomes (2)

  • Change in Behavioral Activation (BA) Quality over Sessions

    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.

    12 weeks, from enrollment to study completion (assessed every 4 weeks)

  • Change in Self-Efficacy

    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.

    12 weeks, from enrollment to study completion (assessed at Baseline and Endline)

Secondary Outcomes (2)

  • System Usability

    End of 12 weeks, at study completion

  • System User Satisfaction

    End of 12 weeks, at study completion

Study Arms (1)

MBPS App

EXPERIMENTAL

Study participants (i.e., non-specialist providers) will use a web application to support measurement-based peer supervision (MBPS) activities (e.g., rating and reviewing therapy sessions) performed with standardized patients in mock scenarios

Device: MBPS App

Interventions

MBPS AppDEVICE

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.

MBPS App

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • years of age or older;
  • English-speaking; and
  • Completed EMPOWER Behavioral Activation training

You may not qualify if:

  • \- Unable to participate in virtual meetings

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Baylor Scott & White Health

Dallas, Texas, 75204, United States

Location

Related Publications (1)

  • Poudyal A, Lewis DM, Taha S, Martinez AJ, Magoun L, Ho YX, Carmio N, Naslund JA, Sanchez K, Lesh N, Patel V. Designing an App to Support Measurement-Based Peer Supervision of Frontline Health Workers Delivering Brief Psychosocial Interventions in Texas: Multimethod Study. JMIR Form Res. 2024 Mar 11;8:e55205. doi: 10.2196/55205.

    PMID: 38466971BACKGROUND

MeSH Terms

Conditions

Anxiety DisordersDepression

Condition Hierarchy (Ancestors)

Mental DisordersBehavioral SymptomsBehavior

Study Officials

  • Yun Xian Ho, PhD

    Dimagi Inc.

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
SINGLE GROUP
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 14, 2025

First Posted

July 24, 2025

Study Start

May 15, 2025

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

August 1, 2026

Last Updated

April 20, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

There is currently no plan to share individual participant data; results will ll be reported in aggregate.

Locations