RECRUITING

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

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Type III Hybrid Effectiveness-Implementation Trial of a Clinical Decision Support System for the Implementation of Problem-Solving Treatment in Community Health Centers

Quick Facts

Study Start:2024-11-06
Study Completion:2028-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06494384

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.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Practitioner Participants. (a) are employed by a clinic that is an OCHIN clinical network member;
  2. * Practitioner Participants. (b) hold a master's degree in social work, psychology, counseling, or a related field;
  3. * Practitioner Participants. (c) provide psychotherapeutic care in the OCHIN network;
  4. * 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;
  5. * Practitioner Participants. (e) are not currently receiving specialized training outside of standard clinic support to implement a depression-specific psychosocial intervention; and
  6. * Practitioner Participants. (f) are English-speaking.
  7. * Client Participants. a) 18+,
  8. * Client Participants. b) English-speaking,
  9. * Client Participants. c) have a diagnosis of unipolar depression per provider report, and
  10. * Client Participants. d) have a PHQ-9 score ≥ 10, which is above the clinical cutoff for depression symptoms.
  1. * Client Participants. (a) history or presence of psychiatric diagnoses other than unipolar, nonpsychotic depression or anxiety disorders,
  2. * Client Participants. (b) active suicidal ideation,
  3. * Client Participants. (c) current alcohol or substance abuse disorders, or
  4. * Client Participants. (d) have dementia
  5. * Client Participants. (e) all exclusion criteria cannot be confirmed via provider report.
  6. * Practitioner Participants. Exclusion criteria are those that do not meet the inclusion criteria listed above.

Contacts and Locations

Study Contact

Helen Haile
CONTACT
206-616-2129
hghaile@uw.edu

Principal Investigator

Patrick Raue, PhD
PRINCIPAL_INVESTIGATOR
University of Washington

Study Locations (Sites)

OCHIN, Inc.
Portland, Oregon, 97228-5426
United States

Collaborators and Investigators

Sponsor: University of Washington

  • Patrick Raue, PhD, PRINCIPAL_INVESTIGATOR, University of Washington

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 Registration Dates

Study Start Date2024-11-06
Study Completion Date2028-03-31

Study Record Updates

Study Start Date2024-11-06
Study Completion Date2028-03-31

Terms related to this study

Additional Relevant MeSH Terms

  • Depression