Methadone Patient Access to Collaborative Treatment
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 102
- 试验地点
- 2
- 主要终点
- methadone treatment retention
研究概览
简要总结
Examine the preliminary effect of the MPACT intervention on methadone treatment retention, in treatment overdose and patient trauma symptoms. The study will also explore the relationship between staff trauma symptoms and MPACT implementation.
详细描述
Specific AIMS:
AIM 1: Develop MPACT through multilevel, iterative planning with OTP staff and people with recent MMT experience.
AIM 2: Conduct a 4-month MPACT pilot test in two AZ OTPs: Mesa (urban) with 50 patients and 22 staff, and Sierra Vista (rural-serving) with 50 patients and 8 staff to:
- Determine MPACT implementation feasibility, acceptability, and preliminary effect on MMT practice change and culture.
- Determine MPACT preliminary effect on MMT retention, in-MMT overdose, and patient PTSS.
- Characterize staff trauma history, PTSS and vicarious trauma, and explore their relationship with MPACT acceptability and implementation fidelity.
AIM 3: Characterize MPACT acceptability, likely adoption, and recruitment feasibility among directors, case managers and counselors from a national random sample of 500 OTPs.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Staff of enrolled opioid treatment programs (methadone clinics) who are involved with methadone treatment
- •Patients receiving methadone at these locations
排除标准
- •Patients not receiving methadone at these locations
- •Staff not involved in methadone treatment at these locations
结局指标
主要结局
methadone treatment retention
时间窗: 4 months (pilot study period)
Retention in methadone treatment (measured by 3 different indicators)
In treatment overdose
时间窗: 4 months (pilot study period)
Reported overdoses during methadone treatment (measured by study constructed algorithm)
次要结局
- Vicarious Trauma symptoms among staff(pilot period of 4 months)
- Trauma symptoms among patients and staff(pilot period of 4 months)