Phone Interview to Prevent Recurring Opioid Overdoses (TTIP-PRO)
Pilot Evaluation of the "Tailored Telephone Intervention Delivered by Peers to Prevent Recurring Opioid-Overdoses"
研究概览
详细说明
研究类型
注册 (预期的)
阶段
- 不适用
联系人和位置
学习地点
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Ohio
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Cincinnati、Ohio、美国、45229
- 3131 Harvey Avenue, Suite 104
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Cincinnati、Ohio、美国、45229
- UC Physicians Company, LLC Opioid Treatment Program
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria for participants (receiving the TTIP-PRO intervention):
- have been treated for an OOD by the UCMC ED within the prior 8 months
- have used heroin and/or abused prescription opioids in the prior 12 months
- be 18 years of age or older at time of enrollment
- be able to provide verbal consent to participate in English
Exclusion Criteria for participants (receiving the TTIP-PRO intervention):
- demonstrate difficulty understanding the study as assessed with four true-false questions (i.e., 1. This is a research study; 2. Your participation is entirely voluntary; 3. You will be asked questions about your risk of opioid overdose.; 4. Your participation will involve several phone calls).
Inclusion Criteria for Peer Interventionists:
- be 18 years of age or older at time of enrollment
- be enrolled in a methadone-maintenance or buprenorphine- maintenance treatment program for at least one year
- report being opioid-abstinent for at least one year
- meet at least one of the following: has experienced/witnessed/lost a family member or friend to an overdose
- be able to provide informed consent in English
Exclusion criteria for Peer Interventionists:
- have significant treatment/clinical concerns as determined by treatment program staff
The primary pool of potential Peer Interventionists will be patients enrolled in the UC Health (University of Cincinnati Physicians Company) methadone-maintenance or buprenorphine- maintenance treatment programs. Recruitment will be through clinic postings and word of mouth. It is estimated that 2-3 Peer Interventionists will be enrolled in the study.
学习计划
研究是如何设计的?
设计细节
- 主要用途:预防
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
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其他:TTIP-PRO
Patients who have experienced an OOD in the past 8 months will be eligible to receive TTIP-PRO.
A letter about the study will be sent to those patients.
Interested patients will call the UC Health staff working on this study.
The intervention entails administering the Personal Opioid-Overdose Risk Survey and the Opioid Overdose and Treatment Awareness Survey to the patient.
The TTIP-PRO computer program uses the information to generate the "Personal Feedback Report", which is used by the Peer Interventionist to provide the intervention.
The TTIP-PRO computer program also creates the "Personal Risk Factors Report" which is mailed to the participant with some other helpful information.
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The peer-delivered TTIP-PRO intervention is designed to: 1).
increase the patient's knowledge of risk factors for OOD, with a particular emphasis on the patient's personal risk factors.
This aim is one of harm reduction and is intended to help patients who continue to abuse opioids to use in a safer manner and 2).For patients who are open to considering treatment, to encourage the patient to get treatment for his/her opioid use disorder.
This goal is based on research findings that effective treatment reduces the risk of OOD.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
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Study Acceptability (proportion of patients who: a). call about the study and b). agree to participate in the study and c). who complete the study.)
大体时间:6 months
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Acceptability of the study will be assessed based on the proportion of patients who: a). call about the study and b). agree to participate in the study and c). who complete the study. Acceptability of the study will be further assessed by peer interventionists who: a). complete the training and b). complete the study (i.e. continue to successfully provide intervention to assigned participants through the end of the study). |
6 months
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
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Impact of TTIP-PRO on knowledge about Opioid Overdose. (will be assessed with a paired difference test (e.g., paired t-test))
大体时间:6 months
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The impact of the TTIP-PRO on knowledge about OOD will be assessed with a paired difference test (e.g., paired t-test).
Finally, summary statistics for the proportion of participants willing to be contacted by a MAT staff member after receiving the TTIP-PRO intervention will be calculated.
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6 months
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合作者和调查者
出版物和有用的链接
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.
TTIP-PRO的临床试验
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Abramson Cancer Center at Penn MedicineNational Cancer Institute (NCI)招聘中
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University of AarhusAarhus University Hospital; TrygFonden, Denmark; Sygekassernes Helsefond; Regional Hospital West... 和其他合作者完全的
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Ludwig-Maximilians - University of MunichTherapiezentrum Burgau完全的
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Medtronic Cardiovascular主动,不招人