RECRUITING

K-ORCA: Testing a Decision Support Tool and Group Process for Selecting Interventions

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

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.

Official Title

Refining and Pilot Testing a Decision Support Intervention to Facilitate Adoption of Evidence-Based Programs to Improve Parent and Child Mental Health

Quick Facts

Study Start:2024-02-01
Study Completion:2027-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06375551

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:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Non-institutionalized
  2. * Adults (18 years or older).
  3. * English-Speaking
  4. * Involved in initial state decision-making related to Family First Prevention Services Act.
  5. * Willing to participate in two data collection occasions.
  6. * Non-institutionalized
  7. * Adults (18 years or older). English-Speaking.
  8. * Involved in ongoing state decision-making related to Family First Prevention Services Act.
  9. * Willing to participate in three measurement occasions.
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Gracelyn Cruden, PhD
CONTACT
843-513-9928
gcruden@chestnut.org
Kelli Wright
CONTACT
kwright@chestnut.org

Principal Investigator

Gracelyn Cruden, PhD
PRINCIPAL_INVESTIGATOR
Chestnut Health Systems

Study Locations (Sites)

Chestnut Health Systems
Eugene, Oregon, 97401
United States

Collaborators and Investigators

Sponsor: Chestnut Health Systems

  • Gracelyn Cruden, PhD, PRINCIPAL_INVESTIGATOR, Chestnut Health Systems

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 Date2024-02-01
Study Completion Date2027-07-31

Study Record Updates

Study Start Date2024-02-01
Study Completion Date2027-07-31

Terms related to this study

Additional Relevant MeSH Terms

  • Child Abuse
  • Decision Making
  • Child Welfare
  • Decision Making, Shared
  • Decision Support Technique
  • Social Facilitation
  • Implementation Science
  • Policy
  • Organizations
  • Consensus
  • Mental Health
  • Family