跳至主要内容
临床试验/NCT06696066
NCT06696066已完成不适用

Pilot Evaluation of a Peer Recovery Support Program Adapted to Target Retention in Clinic-based Medication for Opioid Use Disorder Treatment

Geisinger Clinic1 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2025年2月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
13
试验地点
1
主要终点
Feasibility - Participant Engagement in the Peer Recovery Support Program

研究概览

简要总结

The goal of this pilot study is to evaluate the feasibility and acceptability of implementing a peer recovery support program to support patient engagement in medication treatment for opioid use disorder (MOUD). The program, entitled "Promoting Enhanced Engagement through Recovery Support" (PEERS) was developed in collaboration with community and clinical partners for the MOUD outpatient setting. Information gathered during this pilot study will inform refinements to the program and study components for a future clinical trial that will evaluate the effectiveness of the peer recovery support program in increasing patient retention in MOUD.

The investigators will recruit 12 participants to the pilot study, all of whom will receive the PEERS program. The study will take place in Geisinger outpatient addiction treatment clinics in northeast Pennsylvania. Patients initiating MOUD treatment at one of the clinics will be eligible for participation, and will be recruited via email, patient portal messages, and phone. Each participant will receive the PEERS program, entailing regular sessions with a Certified Recovery Specialist (CRS) for 6 months. Participants will also be asked to complete assessments at baseline and 12 weeks and will be invited to provide qualitative feedback on their experience with the program through an interview conducted between 8-12 weeks. As the focus of the pilot pertains to the feasibility and acceptability of the program and the study components, study outcomes focus on participant engagement in and acceptance of the program, CRS fidelity to the program, barriers to implementation, and feasibility of data collection.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 89 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult ≥ 18 years of age
  • Initiated medication for opioid use disorder at a Geisinger outpatient addiction treatment clinic within the past 45 days
  • Willing to participate in the Peer Recovery Support program
  • Able and willing to provide consent

排除标准

  • Received medication for opioid use disorder at a Geisinger outpatient addiction treatment clinic in the 90 days prior to the treatment initiation date
  • Not proficient in English

研究组 & 干预措施

Peer Recovery Support Pilot Program Implementation and Assessment

Experimental

Participants will be offered services from a certified recovery specialist (CRS; i.e., the Peer Recovery Support program). This will entail a CRS meeting one-on-one with the patient at regular intervals (e.g., weekly) to provide support to the participant for a 6-month period. CRS services are patient-centered and driven by a patient's own recovery goals, thus the frequency, timing, duration, modality (in-person, phone), and location of meetings (in the clinic or in a community setting such as a coffeeshop) are flexible and determined collaboratively by the CRS and patient.

干预措施: PRS Program (Behavioral)

结局指标

主要结局

Feasibility - Participant Engagement in the Peer Recovery Support Program

时间窗: Baseline to 12 weeks

Percent of participants who attended at least 2 sessions with the Certified Recovery Specialist

Acceptability - Participant Alliance With Certified Recovery Specialist

时间窗: 12 weeks

Participants' average scores for the Scales for Participant Alliance with Recovery Coach (SPARC-2); score can range from 1-5 and a high score indicates greater satisfaction with the CRS.

次要结局

  • Feasibility - Feasibility of Assessment Completion(Baseline)
  • Feasibility - Feasibility of Assessment Completion(12 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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