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
調査の概要
詳細な説明
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.
研究の種類
入学 (実際)
連絡先と場所
研究場所
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Pennsylvania
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Pittsburgh、Pennsylvania、アメリカ、15215
- UPMC Magee Womens Hospital
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
サンプリング方法
調査対象母集団
説明
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
研究計画
研究はどのように設計されていますか？
デザインの詳細
コホートと介入
グループ/コホート |
介入・治療 |
|---|---|
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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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この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Themes surrounding mothers' pain/recover experience
時間枠：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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協力者と研究者
スポンサー
捜査官
- 主任研究者：Grace Lim, MD MS、University of Pittsburgh
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。