Obstetric Pain Management for Women With Opioid Use Disorder (QUEST) (QUEST)
Obstetric Pain Management for Women With Opioid Use Disorder: A Longitudinal, Qualitative Mixed-methods Evaluation of Patients and Provider Perspectives
研究概览
详细说明
A fine understanding of the attitudes and beliefs about pain and its management for patients with opioid use disorder is currently lacking. These psychological aspects of pain and analgesia are expected to have significant effects on nociception, pain experience, analgesic efficacy, and opioid requirements and its subsequent risks for relapse/treatment noncompliance. There is also have little understanding of provider-held attitudes and beliefs which can influence pain and its treatment for this population.
The findings from this study will inform patient-centered approaches to pain management for obstetric patients with OUD. They will also shape an appropriate patient-centered research agenda for obstetric pain management in patients with OUD. This work will find new patient-centered endpoints for this special population that may be currently overlooked with existing standard pain assessments.
研究类型
注册 (实际的)
联系人和位置
学习地点
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Pennsylvania
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Pittsburgh、Pennsylvania、美国、15215
- UPMC Magee Womens Hospital
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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
取样方法
研究人群
描述
Inclusion Criteria:
- Pregnant women who are 18 years of age or older
- History of opioid use disorder, on medication assisted therapy
- Currently in their third trimester
Exclusion Criteria:
- Unable to participate in informed consent discussions
- Unable to give informed consent for any reason
- Not fluent in English (surveys are validated in English language)
- Unable to participate fully in all study procedures for any reason
学习计划
研究是如何设计的？
设计细节
队列和干预
团体/队列 |
干预/治疗 |
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Patient participants
This cohort will include pregnant patients with a history of opiate use disorder (OUD) who will be followed from the third trimester of pregnancy until five days postpartum.
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Semi-structured interviews
Validated surveys on pain, fear, anxiety, depression, beliefs
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Provider participants
This cohort will include clinicians who provide care for pregnant patients with OUD.
Providers will be interviewed and will complete one survey cross-sectionally.
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Semi-structured interviews
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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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Themes surrounding mothers' pain/recover experience
大体时间：Through study completion, an average of 6 weeks (from enrollment through labor and delivery)
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The endpoint of this mixed-methods investigation is to identify themes surrounding mothers' pain/recovery experiences that correlate with quantified pain and analgesic needs.
Endpoint will take the form of words/terms, phrases, or sentences.
Identification of these terms, phases, or sentences are not identified a priori in this qualitative investigation.
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Through study completion, an average of 6 weeks (from enrollment through labor and delivery)
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合作者和调查者
调查人员
- 首席研究员：Grace Lim, MD MS、University of Pittsburgh
研究记录日期
研究主要日期
学习开始 (实际的)
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 (实际的)
研究记录更新
最后更新发布 (实际的)
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.
阿片类药物使用障碍的临床试验
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Hospital Universitari Vall d'Hebron Research InstituteInstituto de Salud Carlos III完全的
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Interview的临床试验
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Norwegian Institute of Public HealthStatistics Norway; Society of Interventional Oncology完全的
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