Actively Recruiting
K-ORCA: Testing a Decision Support Tool and Group Process for Selecting Interventions
Led by Chestnut Health Systems · Updated on 2026-03-18
80
Participants Needed
1
Research Sites
65 weeks
Total Duration
On this page
Sponsors
C
Chestnut Health Systems
Lead Sponsor
N
National Institute of Mental Health (NIMH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
K-ORCA: Testing a Decision Support Tool and Group Process for Selecting Interventions
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Non-institutionalized adults aged 18 years or older
- English-speaking
- Involved in initial or ongoing state decision-making related to the Family First Prevention Services Act
- Willing to participate in two or more data collection occasions, including bi-weekly assessments up to two years
You will not qualify if you...
- Not involved in or unable to influence child welfare intervention decisions
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Chestnut Health Systems
Eugene, Oregon, United States, 97401
Actively Recruiting
Research Team
G
Gracelyn Cruden, PhD
CONTACT
K
Kelli Wright
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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