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The time following discharge from psychiatric hospitalization is a high-risk period and has been associated with a range of negative outcomes including high rates of hospital readmission and suicide. The purpose of this proposal is to: 1) create a Peer Specialist facilitated intervention, called Recovery Bridge, designed to facilitate the transition from inpatient psychiatric hospitalization to community living; 2) examine feasibility, fidelity, and acceptability; and preliminarily explore the impact of the intervention on: a) readmission rates and connection to outpatient care compared to a control group identified from administrative data; and b) change in recovery and quality of life measures over time in the intervention participants. Results from the proposed open pilot trial will set the stage for next steps including a larger effectiveness trial followed by a possible hybrid-I effectiveness/implementation trial to inform future dissemination and implementation of the intervention more broadly across the VA.
Background: The time following discharge from psychiatric hospitalization is a high-risk period and has been associated with a range of negative outcomes, including high rates of hospital readmission and suicide (1). Because the evidence for transitional discharge interventions with bridging components is mixed and limited in terms of how Peer Specialists (PS) can help support such interventions, additional research is needed. This proposal calls for the development and preliminary evaluation of a PS facilitated technology-supported intervention based on the existing and frequently used My Recovery Plan program. However, to date, no studies have examined use of this tool to improve post-hospital discharge outcomes. Given the importance of the problem for the VA, and the fact that the VA has both a large PS infrastructure that is valued by both professional providers and Veterans, the investigators' work offers sound justification and the unique opportunity to test the proposed intervention in a single integrated system of inpatient and outpatient services.
Significance: The significance of this project lies in its ability to actively address an important gap in the research, namely PS interventions focused on reducing readmission and supporting recovery-oriented outcomes in Veterans. Further relating to important HSR&D priorities the project is designed to advance scientific knowledge and clinical practice in the areas of access to care, mental health, and suicide prevention.
Innovation and Impact: A key innovation of the proposed research is the potential to efficiently optimize existing resources to target the widespread challenges associated with transitioning out of acute inpatient settings and effectively connect Veterans to preferred services (in this case peer support) in order to prevent re-admission, and improve utilization of VA outpatient mental health services. Finally, in relationship to impact, Recovery Bridge has potential to result in improvement across multiple clinical and functional outcomes that are applicable to a broad Veteran population (rather than only in small select diagnostically specific subpopulations).
Specific Aim 1: Integrate the My Recovery Plan tool and existing PS tools and strategies to develop a manualized intervention called Recovery Bridge for use by VA PS working to help Veterans make the transition from acute inpatient psychiatric hospitalization to community living.
Specific Aim 2: Complete an open pilot trial (n=15) to examine the feasibility, fidelity, and acceptability of the Recovery Bridge intervention in relation to well specified benchmarks supporting continued and expanded investigation.
[Specific Aim 3: As part of the open pilot trial: 1) explore the impact of the intervention on readmission rates (at 30 and 90 days), and connection to outpatient care compared to a control group (n=15) identified from administrative data, and; 2) explore the change in recovery and Quality of Life measures over time in the intervention participants].
Methodology: Source documents described in the proposal will be used to create the Recovery Bridge intervention (as Specified in Aim 1). Quantitative, qualitative, and administrative services data the investigators will be used to complete an open trial of the intervention (as specified in Aim 2 and Aim 3).
Next Steps: Benchmarks across the domains of feasibility, fidelity, and acceptability; as well as exploratory outcomes specified in Aim 3, will be used to inform next steps including a larger effectiveness trial followed by a possible hybrid-I effectiveness/implementation trial to inform future dissemination and implementation of the intervention more broadly across the VA.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Recovery Bridge | Experimental | Open trial single arm pilot study |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Recovery Bridge | Behavioral | Recovery Bridge is a Peer Specialist facilitated intervention designed to help Veterans being discharged from an inpatient psychiatric hospitalization bridge the gap to outpatient care and community living |
| Measure | Description | Time Frame |
|---|---|---|
| Feasibility 1: Recruitment Benchmark | Recruitment (number consented divided by number approached) | 3 months |
| Feasibility 2: Intervention Engagement (Percentage of Sample That Completes at Least 3 Intervention Sessions-with One of the Three Occurring Inpatient | Percentage of sample that completes at least 3 intervention sessions-with one of the three occurring inpatient | 3 months |
| Feasibility 3: Drop Out Rate (Percent That Did Not Complete Post-intervention Assessment) | Drop out Rate: Percent that do not complete post-intervention assessment (based on count of participants) | 3 months |
| Fidelity | Greater than 90% of all Adherence and Competence Items Rated as Acceptable or Higher. Higher ratings of acceptability are considered to be the better outcome. | 3 months |
| Acceptability (Patient Satisfaction Questionnaire--administered Post Intervention) | Score of 26 percent or higher on Patient Satisfaction Questionnaire. Scale ranges from 8-32, higher score is associated with "better outcome" (i.e. higher satisfaction). | 3 months |
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Inclusion Criteria:
Inclusion Criteria for active sample:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Richard W Goldberg, PhD | Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD | Baltimore | Maryland | 21201 | United States |
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Single Arm Open Trial (for primary outcomes)
The primary outcomes in this open trial were only for the single arm actively recruited for the study
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| ID | Title | Description |
|---|---|---|
| FG000 | Recovery Bridge | Recovery Bridge is a Peer Specialist facilitated intervention designed to help Veterans being discharged from an inpatient psychiatric hospitalization bridge the gap to outpatient care and community living |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
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| ID | Title | Description |
|---|---|---|
| BG000 | Recovery Bridge | Recovery Bridge is a Peer Specialist facilitated intervention designed to help Veterans being discharged from an inpatient psychiatric hospitalization bridge the gap to outpatient care and community living |
| Units | Counts |
|---|---|
| Participants |
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| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Feasibility 1: Recruitment Benchmark | Recruitment (number consented divided by number approached) | Overall Number of Participants Analyzed reflects the number of participants approached | Posted | Number | participants | 3 months |
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from baseline until post-assessment (up to 3 months)
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Recovery Bridge | Recovery Bridge is a Peer Specialist facilitated intervention designed to help Veterans being discharged from an inpatient psychiatric hospitalization bridge the gap to outpatient care and community living |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Richard Goldberg, Ph.D. (Principal Investigator) | VISN 5 MIRECC | 410-637-1851 | Richard.Goldberg@va.gov |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Jun 26, 2025 | Dec 11, 2025 | Prot_SAP_001.pdf |
| ICF | No | No | Yes | Informed Consent Form | Oct 31, 2023 | Feb 4, 2025 | ICF_000.pdf |
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| ID | Term |
|---|---|
| D001523 | Mental Disorders |
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Open Pilot Trial (n=15) to examine feasibility, fidelity, and acceptability of study intervention (called Recovery Bridge)
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| years |
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| Sex: Female, Male | Count of Participants | Participants | No |
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| Race (NIH/OMB) | Count of Participants | Participants | No |
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| Primary | Feasibility 2: Intervention Engagement (Percentage of Sample That Completes at Least 3 Intervention Sessions-with One of the Three Occurring Inpatient | Percentage of sample that completes at least 3 intervention sessions-with one of the three occurring inpatient | Posted | Count of Participants | Participants | 3 months |
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| Primary | Feasibility 3: Drop Out Rate (Percent That Did Not Complete Post-intervention Assessment) | Drop out Rate: Percent that do not complete post-intervention assessment (based on count of participants) | Posted | Count of Participants | Participants | 3 months |
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| Primary | Fidelity | Greater than 90% of all Adherence and Competence Items Rated as Acceptable or Higher. Higher ratings of acceptability are considered to be the better outcome. | among the sessions reviewed for fidelity across the two criteria (adherence and competence) | Posted | Number | % of reviewed items meeting fidelity | 3 months | Number of Fidelity Items Analyzed | Number of Fidelity Items Analyzed |
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| Primary | Acceptability (Patient Satisfaction Questionnaire--administered Post Intervention) | Score of 26 percent or higher on Patient Satisfaction Questionnaire. Scale ranges from 8-32, higher score is associated with "better outcome" (i.e. higher satisfaction). | only those completing intervention | Posted | Mean | Standard Deviation | score on a scale | 3 months |
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| 0 |
| 15 |
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| 15 |
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| 15 |
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