跳至主要内容
临床试验/NCT02660619
NCT02660619已完成不适用

Validation of PRISM-5-Op, Measure Of Addiction To Prescription Opioid Medication

Member Companies of the Opioid PMR Consortium0 个研究点目标入组 606 人开始时间: 2015年11月17日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
606
主要终点
Diagnoses of Addiction to Prescription Opioids via PRISM-5-Op

研究概览

简要总结

The purpose is to validate the PRISM-5-Op as a measurement of prescription opioid substance use disorder.

详细描述

"Based on a review of the literature, the Food and Drug Administration (FDA) concluded that more data are needed regarding the serious risks of misuse, abuse, addiction, overdose, and death associated with the long-term use of extended release/long acting (ER/LA) opioid analgesics. Thus, the FDA is requiring that ER/LA opioid analgesic drug sponsors conduct post-marketing studies to assess these risks. The present study, PMR Study #2065-2, focuses on addiction, and addresses the FDA requirement to conduct a validation study of the measure of addiction that will be used in PMR Study #2065-1.

The primary objective for Study 2b is to validate PRISM-5-Op measures of DSM-5 prescription opioid SUD/addiction in patients who have, or have had, a prescription for opioids for at least 30 days to treat chronic pain"

研究设计

研究类型
Observational
观察模型
Other
时间视角
Cross Sectional

入排标准

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

入选标准

  • Has or has had a prescription for opioids for chronic pain for at least 30 days
  • Age 18 years or older and English-speaking
  • Willing and able to provide informed consent"

排除标准

  • Patient has a hearing or vision impairment that would preclude an interview or completion of self-administered questionnaires
  • Patient too cognitively impaired to give informed consent or participate in the evaluations.

结局指标

主要结局

Diagnoses of Addiction to Prescription Opioids via PRISM-5-Op

时间窗: Up to 14 days (reliability determined by re-interviews 1-14 days after first interview)

PRISM-5-Op diagnoses of DSM-5 SUD/addiction to prescription opioids. These diagnoses will be in two forms: unadjusted, meaning that the criteria will be rated positive if present without regard to the intent of the behavior, and adjusted, i.e., that criteria will be rated positive only if structured evaluation indicates that they represent addiction indicators (non-therapeutic intent) rather than treatment of pain (therapeutic intent).

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

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