Patient Navigation and Tailored Treatment Planning in Latina Patients With Breast Cancer
Breast Cancer Patient Navigation and Tailored Treatment Planning: A Process Evaluation Study for LAC+USC Patient Navigation, Treatment Planning, and Ongoing Support for Latina Women
調査の概要
詳細な説明
PRIMARY OBJECTIVES:
I. Successful navigation of patients being screened or treated for breast cancer through the continuum of their care (from visit to visit; from surgical care to radiologic care to oncologic care; from oncologic care to supportive care; etc).
II. Supply individualized in-language treatment summaries and follow-up care plans to enrolled patients.
III. Supply tailored in-language survivorship plan summaries to enrolled patients.
OUTLINE:
Patients receive treatment summaries and plan report that captures patient data through the use of an "intake checklist" completed during the initial consultation with the breast oncology team and used to guide referrals to existing services and programmed with generic information related to disease and treatment management plan. Additional elements, such as psycho-social services, exercise, and/or nutrition, identified by the patient self-report, will be incorporated. Patients also complete 3 questionnaires at each clinic visit.
After completion of study, patients are followed up at 6 months or 12 months.
研究の種類
入学 (実際)
連絡先と場所
研究場所
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California
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Los Angeles、California、アメリカ、90033
- USC / Norris Comprehensive Cancer Center
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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:
- Patients receiving ongoing care at LAC+USC
- Self-identified as Latina (or Hispanic)
- Known or suspected breast cancer
- Being seen in a breast cancer high risk, screening or prevention program or clinic or in one of the breast cancer clinics (surgical or medical oncology)
Exclusion Criteria:
- Inability to sign informed consent or complete questionnaires and forms
- Self-identified as non-Latina (or non-Hispanic)
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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Observational (treatment summaries and plan report)
Patients receive treatment summaries and plan report that captures patient data through the use of an "intake checklist" completed during the initial consultation with the breast oncology team and used to guide referrals to existing services and programmed with generic information related to disease and treatment management plan.
Additional elements, such as psycho-social services, exercise, and/or nutrition, identified by the patient self-report, will be incorporated.
Patients also complete 3 questionnaires at each clinic visit.
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補助研究
他の名前：
アンケートに記入する
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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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Number of missed appointments from the time of initial diagnosis to the completion of primary treatment (chemotherapy, surgery and radiation as applicable) as measured by CCCQ
時間枠：Up to 12 months
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Questionnaire scores will be expressed as median values with 95% confidence intervals.
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Up to 12 months
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Number of patients enrolled on clinical trials (interventional and non-interventional)
時間枠：Up to 12 months
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Number of patients enrolled on clinical trials (interventional and non-interventional) will be quantified and compared to historical controls.
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Up to 12 months
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Number of special referrals made
時間枠：Up to 12 months
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Number of special referrals made (eg.
social worker, genetic counseling, fertility) through the navigation system will quantified and compared to historical controls.
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Up to 12 months
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Overall experience with breast cancer (broadly) and at LAC+USC as measured by experience-based questionnaire
時間枠：Up to 12 months
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Up to 12 months
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Usefulness, accessibility, and quality of the patient navigation model as measured by Continuity/Coordination of Care Questionnaire (CCCQ)
時間枠：Up to 12 months
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Means and standard deviations will be summarized per outcome measures at 3, 6, and 12 months after baseline, and 95% confidence intervals for the difference in means will be calculated for each assessment time for total scores and subscale scores.
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Up to 12 months
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協力者と研究者
捜査官
- 主任研究者：Heather Macdonald、University of Southern California
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 (見積もり)
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。
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