Mental Health Clinical Trial
— K-ORCAOfficial title:
Refining and Pilot Testing a Decision Support Intervention to Facilitate Adoption of Evidence-Based Programs to Improve Parent and Child Mental Health
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.
Status | Not yet recruiting |
Enrollment | 80 |
Est. completion date | July 31, 2027 |
Est. primary completion date | July 31, 2027 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Non-institutionalized - Adults (18 years or older). - English-Speaking Aim 1: - Involved in initial state decision-making related to Family First Prevention Services Act. - Willing to participate in two data collection occasions. Aim 2: - Non-institutionalized - Adults (18 years or older). English-Speaking. - Involved in ongoing state decision-making related to Family First Prevention Services Act. - Willing to participate in three measurement occasions. Aim 3: -Willing to participate in multiple (bi-weekly up to two years) measurement occasions. Exclusion Criteria: -Not involved in or potentially influencing child welfare intervention decisions |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
---|---|
Chestnut Health Systems | National Institute of Mental Health (NIMH) |
Alley ZM, Chapman JE, Schaper H, Saldana L. The relative value of Pre-Implementation stages for successful implementation of evidence-informed programs. Implement Sci. 2023 Jul 21;18(1):30. doi: 10.1186/s13012-023-01285-0. — View Citation
Cruden G, Frerichs L, Powell BJ, Lanier P, Brown CH, Lich KH. Developing a Multi-Criteria Decision Analysis Tool to Support the Adoption of Evidence-Based Child Maltreatment Prevention Programs. Prev Sci. 2020 Nov;21(8):1059-1064. doi: 10.1007/s11121-020-01174-8. Epub 2020 Oct 11. — View Citation
Oetzel JG, Wallerstein N, Duran B, Sanchez-Youngman S, Nguyen T, Woo K, Wang J, Schulz A, Keawe'aimoku Kaholokula J, Israel B, Alegria M. Impact of Participatory Health Research: A Test of the Community-Based Participatory Research Conceptual Model. Biomed Res Int. 2018 Apr 24;2018:7281405. doi: 10.1155/2018/7281405. eCollection 2018. — View Citation
Weiner BJ, Lewis CC, Stanick C, Powell BJ, Dorsey CN, Clary AS, Boynton MH, Halko H. Psychometric assessment of three newly developed implementation outcome measures. Implement Sci. 2017 Aug 29;12(1):108. doi: 10.1186/s13012-017-0635-3. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Mean changes in decision assumptions, decision goals Pre and Immediately Post-intervention | A two-item, quantitative measure will inquire about assumptions and goals in the decision to adopt an intervention. This uses a 5-point Likert scale ranging from 1 (Strongly disagree) to 5 (Strongly Agree). This outcome is part of Aim 2b: Decision quality based on intervention fit to local context. | Baseline; Immediately Post-intervention | |
Primary | Mean changes in decision experience quality pre-post intervention | This will be measured across five validated, quantitative sub-scales from a measure of community partnered research: Partner Values, Synergy, Conflict and Cooperation, Participation, Participatory decision-making. Each scale has a range of 1 (Strongly Disagree) to 5 (Strongly Agree). | Baseline; Immediately Post-intervention | |
Primary | Mean changes in decision commitment pre-post intervention | A two-item, Likert-scale measure regarding the decision maker's confidence in and commitment to implementing the selected intervention(s) will be gathered using a two-item measure. This uses a 5-point Likert scale ranging from 1 (Strongly disagree) to 5 (Strongly Agree). These scales relate to Aim 2a: decision experience quality. | Baseline; Immediately Post-intervention | |
Primary | Mean changes in perceived potential community health impact pre-post intervention | This will be measured across a validated, quantitative sub-scale from a measure for community partnered research: Community Health Improvement. This scale has a range of 1 (Strongly Disagree) to 5 (Strongly Agree). This is part of Aim 2b: Decision quality. | Baseline; Immediately Post-intervention; 12-month follow-up | |
Primary | Descriptive changes in ordinal intervention rankings assisted (with ORCA) compared to unassisted (no ORCA) | Decision makers will rank interventions in an ordinal manner at baseline using a study-specific survey. Rankings will be calculated post-intervention by ORCA as a function of completing the ORCA tool. The number of ordinal rankings will depend on the number of interventions considered, to be determined by participants. A rank of 1 = highest, followed by 2 ...n. This is part of Aim 2c: Decision quality. | Baseline; Immediately Post-intervention | |
Primary | Qualitatively described rationale for program adoption from pre-post intervention | This is a study-specific, short, open-ended survey to understand decision makers' rationale for adopting programs during initial Family First Prevention Services Act decisions. There is no scale for the items, given the qualitative, open-ended nature. These are one survey of similar, but related constructs of intervention feasibility, acceptability, and appropriateness. This is part of Aim 2c: Decision quality. | Baseline; Immediately Post-intervention | |
Primary | Descriptive, mean group-level changes in perceived feasibility of intervention Pre-post intervention | The validated, quantitative Feasibility of Intervention Measure (FIM) will be used to assess perceived implementation feasibility for each intervention considered with ORCA. Scale ranges from 1 (Completely Disagree) to 5 (Completely Agree). This outcome is part of Aim 2b regarding decision quality operationalized as intervention fit to local context. | Baseline; Immediately Post-intervention; 12-month post-intervention | |
Primary | Descriptive, mean group-level changes in perceived acceptability of intervention for implementation | The validated, quantitative Acceptability of Intervention Measure (AIM) will be used to assess perceived implementation feasibility for each intervention considered with ORCA. Scale ranges from 1 (Completely Disagree) to 5 (Completely Agree). This outcome is part of Aim 2b regarding decision quality operationalized as intervention fit to local context. | Baseline; Immediately Post-intervention; 12-month post-intervention | |
Primary | Descriptive, mean group-level changes in perceived appropriateness of intervention for implementation | The validated, quantitative Intervention Appropriateness Measure (IAM) will be used to assess perceived acceptability for each intervention considered with ORCA. Scale ranges from 1 (Completely Disagree) to 5 (Completely Agree). This outcome is part of Aim 2b regarding decision quality operationalized as intervention fit to local context. | Baseline; Immediately Post-intervention; 12-month post-intervention | |
Primary | Descriptive differences in implementation process fidelity (activities completed) for interventions adopted with ORCA | A validated measure of implementation activities across 8 stages and 3 phases will be used (Universal Stages of Implementation Completion). Dates are recorded for each activity to be reported or as missing the date, but still being completed. One of the results for the calculated scores is the proportion of activities completed. A higher proportion of activities is generally positive. | Immediately Post-intervention; bi-weekly through 12-month post-intervention | |
Primary | Descriptive differences in implementation process fidelity (timing) for interventions adopted with ORCA | A validated measure of implementation activities across 8 stages and 3 phases will be used (Universal Stages of Implementation Completion). Dates are recorded for each activity to be reported or as missing the date, but still being completed. One of the results for the calculated scores is the duration (time elapsed). The ideal duration depends on the proportion score. | Immediately Post-intervention; bi-weekly through 12-month post-intervention | |
Secondary | Qualitative changes in decision reasoning pre- post-intervention | Group discussion transcripts will be analyzed using directed content analysis to identify themes. At baseline and post-intervention, a single-item, study-specific questionnaire will ask participants to express their rationale for adopting the selected intervention(s). | Baseline; Immediately Post-intervention | |
Secondary | Qualitative changes in decision goals pre- post-intervention | Group discussion transcripts will be analyzed using directed content analysis to identify themes. At baseline and post-intervention, a single-item, study-specific questionnaire (the same as in Outcome 12) will ask participants to express their rationale for adopting the selected intervention(s). | Baseline; Immediately Post-intervention | |
Secondary | Qualitative changes in decision consensus pre- post-intervention | Group discussion transcripts will be analyzed using directed content analysis to identify themes. At baseline and post-intervention, a single-item, study-specific questionnaire (the same as in Outcome 12) will ask participants to express their rationale for adopting the selected intervention(s). | Baseline; Immediately Post-intervention | |
Secondary | Time to adoption or re-adoption of interventions with ORCA | Days elapsed from completing ORCA initial time to official decision regarding adopting or re-adopting an intervention. This outcome relates to Aim 2a: decision process quality. | Baseline to adoption of an intervention for implementation, assessed for up to 24 months |
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