Cervical Ca PROs in Clinical Practice
キーワード
概要
日付
最終確認済み: | 03/31/2019 |
最初に提出された: | 02/06/2017 |
提出された推定登録数: | 02/06/2017 |
最初の投稿: | 02/08/2017 |
最終更新が送信されました: | 04/23/2019 |
最終更新日: | 04/24/2019 |
実際の研究開始日: | 02/26/2017 |
一次完了予定日: | 10/31/2020 |
研究完了予定日: | 10/31/2020 |
状態または病気
介入/治療
Other: Cervical Cancer Patients
Other: Oncologist
段階
アームグループ
腕 | 介入/治療 |
---|---|
Cervical Cancer Patients Adult, English-speaking cervical cancer patients, who have been treated with curative intent chemo-radiotherapy. | Other: Cervical Cancer Patients Disease specific Patient Reported Outcome measurement tool developed by the European Organization for Research and Treatment of Cancer (EORTC). This questionnaire covers symptoms common to women with cervical cancer and captures the impact of disease and/or treatment on domains including: urologic and gastro-intestinal symptoms, sexual functioning and body image. |
Oncologist Oncologists who treat cervix cancer, with at least one consenting patient enrolled in the study. | Other: Oncologist This Feedback form to be completed by oncologists who have had at least one consenting patient participating in this study. |
適格基準
研究の対象となる年齢 | 18 Years に 18 Years |
研究に適格な性別 | All |
サンプリング方法 | Non-Probability Sample |
健康なボランティアを受け入れる | はい |
基準 | Patient Inclusion Criteria: 1. Adult (> 18 years) English speaking patients 2. Treated with curative intent with chemo-radiotherapy 3. Seen in routine clinic follow-up within 5 years post completion of treatment Patient Exclusion Criteria: 1. Patients at their anticipated last clinic visit prior to cancer center discharge 2. Patients unable to complete the EORTC QLQ CX-24 questionnaire due to inability to read or write. 3. Non-English speaking patients 4. Patients of the principal investigator. The rationale for this is that patients of the principal investigator who complete the Feedback form may be biased and this may be reflected in the results. Oncologist Inclusion Criteria: 1. Oncologists who treat cervix cancer 2. Oncologists with at least one consenting patient enrolled in the study Oncologist Exclusion Criteria: 1) Principal investigator listed on the protocol. The rationale for this is that oncologists who are also investigators on this study may have inherent bias in the study which may be reflected in the results of the Feedback form. |
結果
主な結果の測定
1. Percentage of EORTC QLQ CX24 questionnaire completed [9 months]
2. Percentage of favorable scores (Agree or strongly agree) on Feedback Form [9 months]