跳至主要内容
临床试验/NCT05758376
NCT05758376
已完成
不适用

Recovery Bridge: A Peer Facilitated Intervention to Help Bridge the Transition From Psychiatric Inpatient Hospitalized to Living in the Community

VA Office of Research and Development1 个研究点 分布在 1 个国家目标入组 15 人2023年12月1日
干预措施Recovery Bridge

概览

阶段
不适用
干预措施
Recovery Bridge
疾病 / 适应症
Mental Illness
发起方
VA Office of Research and Development
入组人数
15
试验地点
1
主要终点
Feasibility 1: Recruitment Benchmark
状态
已完成
最后更新
10天前

概览

简要总结

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.

详细描述

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.

注册库
clinicaltrials.gov
开始日期
2023年12月1日
结束日期
2024年12月31日
最后更新
10天前
研究类型
Interventional
研究设计
Single Group
性别
All

研究者

责任方
Sponsor

入排标准

入选标准

  • Inclusion Criteria for active sample:
  • 18 years of age or older
  • enrolled in the inpatient program
  • planned discharge to the community

排除标准

  • Inability to provide consent
  • No access to either a computer or a telephone after discharge (as at least one of these will be needed should the Veteran and PS interventionist decide to continue to meet remotely)

研究组 & 干预措施

Recovery Bridge

Open trial single arm pilot study

干预措施: Recovery Bridge

结局指标

主要结局

Feasibility 1: Recruitment Benchmark

时间窗: 3 months

Recruitment (number consented divided by number approached)

Feasibility 2: Intervention Engagement (Percentage of Sample That Completes at Least 3 Intervention Sessions-with One of the Three Occurring Inpatient

时间窗: 3 months

Percentage of sample that completes at least 3 intervention sessions-with one of the three occurring inpatient

Feasibility 3: Drop Out Rate (Percent That Did Not Complete Post-intervention Assessment)

时间窗: 3 months

Drop out Rate: Percent that do not complete post-intervention assessment (based on count of participants)

Fidelity

时间窗: 3 months

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.

Acceptability (Patient Satisfaction Questionnaire--administered Post Intervention)

时间窗: 3 months

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).

研究点 (1)

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