Decision Support Tools for Mental Health
(K-ORCA Trial)
Trial Summary
What is the purpose of this trial?
This proposal responds to NIMH Objective 4.2.c to develop "decision-support tools and technologies that increase the effectiveness and continuous improvement of mental health interventions" by leveraging the Family First Prevention Services Act (FFPSA) policy opportunity. First, a web-based platform to host (a) a decision-support tool and (b) automated facilitation for group decisions with the tool will be developed with state partners' feedback. Next, decision makers leading their states' FFPSA quality improvement efforts will be engaged to pilot a decision-support intervention comprised of the tool and live or automated facilitation, and to evaluate the implementation quality of evidence-based programs adopted with the decision-support intervention.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications.
What data supports the effectiveness of the treatment Optimizing Responses with Collaborative Assessments-Automated (ORCA-A) and Optimizing Responses with Collaborative Assessments-Live (ORCA-L)?
Research shows that using routine outcome monitoring (ROM) and feedback tools can improve mental health treatment outcomes by helping clinicians make better decisions. Similar tools, like the ACORN Toolkit, have been shown to enhance psychotherapy results by providing valuable feedback to therapists.12345
How does the Decision Support Tools for Mental Health treatment differ from other treatments for mental health conditions?
This treatment is unique because it uses decision support tools, which are computer-based systems that help clinicians and patients make informed decisions by providing evidence-based recommendations and personalized feedback. Unlike traditional treatments, these tools facilitate collaborative decision-making and can be accessed via the internet or smartphones, allowing for real-time tracking and adjustment of treatment plans.678910
Research Team
Gracelyn Cruden, PhD
Principal Investigator
Chestnut Health Systems
Eligibility Criteria
This trial is for adults over 18 who speak English, are not institutionalized, and are involved in state decision-making related to the Family First Prevention Services Act. They must be willing to participate in multiple data collection events.Inclusion Criteria
Timeline
Development
Development of a web-based platform to host the decision-support tool and automated facilitation strategy with input from decision makers.
Pilot Testing
Decision makers pilot the decision-support intervention comprised of the tool and live or automated facilitation.
Follow-up
Participants are monitored for the quality of decision experiences, processes, and outcomes post-intervention.
Treatment Details
Interventions
- Optimizing Responses with Collaborative Assessments-Automated (ORCA-A)
- Optimizing Responses with Collaborative Assessments-Live (ORCA-L)
Find a Clinic Near You
Who Is Running the Clinical Trial?
Chestnut Health Systems
Lead Sponsor
National Institute of Mental Health (NIMH)
Collaborator