Implementation of Problem-Solving Treatment in Community Health Centers (PST-Aid)

University of Washington

Status: Enrolling

Conditions: Depression

Treatments: Behavioral: Problem Solving Treatment as usual (PST as usual); Behavioral: Problem Solving Treatment Aid (PST-Aid)

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT06494384

P50MH115837-06 (U.S. NIH Grant/Contract)

STUDY00020564

Details and patient eligibility

About

Although evidence-based clinical interventions (CI) are a preferred treatment option for patients with depression, CIs are rarely available in community primary care settings. When available, CIs are often delivered with poor fidelity and abandoned by practitioners during the initial months post-training. Identifying effective implementation strategies to support the adoption, reach, and sustained use with fidelity of these CIs could enhance the effectiveness of primary care-based treatment of depression, as primary care is where most treatment for this disorder is delivered. Current models of primacy care practitioner training and supervision follow standard formal didactic procedures that might not be sufficient for successful adoption, high-fidelity delivery, and sustainment of CIs. Automated decision support tools and feedback systems embedded in health informatics technology have been found to be effective in supporting the use of best practices and hence might be useful for the transition from training to sustained CI use. In practice, however, these tools are ignored by practitioners, have mixed success on outcomes, and can hinder clinical care owing to poor design. Problem Solving Treatment Aid (PST-Aid), an educate and reorganize implementation strategy, is a web-based app that promotes practitioner-client collaboration in the use of PST for goal setting and action planning. A pilot randomized trial comparing Problem Solving Treatment (PST) training-as-usual to training plus PST-Aid found PST-Aid was deemed to be appropriate and usable to both practitioner and client users with preliminary support for benefits in depression outcomes.

Full description

This study is a hybrid type III effectiveness-implementation randomized clinical trial comparing standard PST implementation with PST augmented by the PST-Aid implementation strategy. The study will test whether:

1. PST Aid results in improved implementation outcomes (initial and sustained fidelity, adoption, reach, and reduced reactive adaptations);
2. Changes in usability, engagement, and appropriateness mediate the effect of PST Aid on implementation outcomes; and
3. PST Aid is more effective in reducing client depressive symptoms and improving functioning.

Enrollment: 410 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Practitioner Participants. (a) are employed by a clinic that is an OCHIN clinical network member;
• Practitioner Participants. (b) hold a master's degree in social work, psychology, counseling, or a related field;
• Practitioner Participants. (c) provide psychotherapeutic care in the OCHIN network;
• Practitioner Participants. (d) have not previously received formal training in PST as defined by University of Washington Advancing Integrated Mental Health Solutions Center (AIMS) criteria;
• Practitioner Participants. (e) are not currently receiving specialized training outside of standard clinic support to implement a depression-specific psychosocial intervention; and
• Practitioner Participants. (f) are English-speaking.
• Client Participants. a) 18+,
• Client Participants. b) English-speaking,
• Client Participants. c) have a diagnosis of unipolar depression per provider report, and
• Client Participants. d) have a PHQ-9 score ≥ 10, which is above the clinical cutoff for depression symptoms.

Exclusion criteria

• Client Participants. (a) history or presence of psychiatric diagnoses other than unipolar, nonpsychotic depression or anxiety disorders,
• Client Participants. (b) active suicidal ideation,
• Client Participants. (c) current alcohol or substance abuse disorders, or
• Client Participants. (d) have dementia
• Client Participants. (e) all exclusion criteria cannot be confirmed via provider report.
• Practitioner Participants. Exclusion criteria are those that do not meet the inclusion criteria listed above.

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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410 participants in 2 patient groups

Problem Solving Treatment as usual (PST as usual)

Active Comparator group

Description:

Participants in this arm will receiving training in PST as usual.

Treatment:

Behavioral: Problem Solving Treatment as usual (PST as usual)

Problem Solving Treatment Aid (PST-Aid)

Experimental group

Description:

Participants in this arm will receiving training in PST with PST-Aid.

Treatment:

Behavioral: Problem Solving Treatment Aid (PST-Aid)