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治験 NCT07030686(対象:生存、再発性、再発、癌、寛解)は募集中です。詳細は治験レーダーのタイル表示と AI 発見ツールで確認するか、ここで質問してください。 | ||
フィルター基準に一致する試験が1件見つかりました
タイル表示
Association Between Exercise, Patient-Reported Outcomes, and Clinical Events in Adult Cancer Survivors
治験(臨床試験)の詳細は主に英語で提供されています。しかし、治験レーダーAIが支援できます!「治験を説明」をクリックして、選択した言語で試験情報を表示し、議論してください。
治験番号 NCT07030686 は 観察研究 臨床試験 で、生存、再発性、再発、癌、寛解 に関するものです。現在は 募集中 で、2020年3月19日 から開始しています。1,000 名の参加者 の募集が計画されています。この治験は メモリアル・スローン・ケタリングがんセンター によって主催され、2026年3月19日 に完了予定です。ClinicalTrials.gov からの最新更新日は 2025年11月26日 です。
概要
This protocol is a retrospective study using observational data to conduct a target trial emulation to examine the association of exercise on cancer specific endpoints and other clinical outcomes in cancer survivors.
公式タイトル
Association Between Exercise, Patient-Reported Outcomes, and Clinical Events in Adult Cancer Survivors
疾患/病気
生存再発性再発癌寛解その他の研究識別子
- 20-101
NCT番号
開始日
2020-03-19
最終更新日
2025-11-26
終了予定日
2026-03-19
目標参加者数
1,000
試験の種類
観察研究
状況
募集中
キーワード
Survivorship
Exercise
cancer survivor
adult cancer survivor
no evidence of disease
20-101
Memorial Sloan Kettering Cancer Center
Exercise
cancer survivor
adult cancer survivor
no evidence of disease
20-101
Memorial Sloan Kettering Cancer Center
群(アーム)/介入
| 参加グループ/群 | 介入/治療法 |
|---|---|
Arm 1: Usual Care | 該当なし |
Arm 2: Exercise | 運動 Exercise following completion of active treatment for the primary index cancer |
主要評価項目
| 評価指標 | 指標の説明 | 時間枠 |
|---|---|---|
Invasive disease-free survival (IDFS) | To estimate the association of exercise vs. usual care (control) with invasive disease-free survival (IDFS) among patients following the completion of active treatment for the primary index cancer being monitored at MSK. | 5 years |
適格基準
対象年齢
成人, 高齢者
試験の最低年齢
18 Years
対象性別
全て
健康なボランティアを受け入れる
はい
Target trial (ideal RCT)
- Adult (≥18 years of age) patients with history of primary invasive cancer under surveillance at Memorial Sloan Kettering Cancer Center (MSK).
- Completion of an exercise survey (baseline) as part of MSK Cancer Survivorship Program and completion of a historical survey in the MSK Cancer Survivorship Program 9-15 months (time th) prior reporting non-exercising status [i.e., reporting <10 metabolic equivalent-hours per week (MET-h/week)]. Patients completing an additional exercise survey between th and baseline are excluded.
- No evidence of recurrent or metastatic disease in the 15 months prior to the baseline exercise assessment
- Completion of all definitive primary adjuvant therapy (e.g., chemotherapy, radiotherapy, targeted therapy) at least 3 months prior to completion of the historical exercise survey in a MSK Cancer Survivorship Program. Adjuvant hormonal therapy is permitted at any time.
- Undergoing surveillance in the Cancer Survivorship Program at MSK
Emulation using observational data
- Adult (≥18 years of age) cancer survivors under surveillance at Memorial Sloan Kettering Cancer Center (MSK) between 2011 and 2023.
- Assessment of self-reported exercise status via completion of an exercise survey as part of MSK Cancer Survivorship Program standard intake (baseline assessment).
- Non-exercising (i.e., reporting <5 MET-h/week) via completion of an exercise survey as part of MSK Cancer Survivorship Program standard intake 9-15 months prior to the baseline exercise assessment (historical exercise survey).
- Documented history of the following absolute contraindications to moderate-intensity exercise at any time prior to the baseline exercise assessment, assessed using the Elixhauser ICD codes: Congestive heart failure, valvular disease, chronic pulmonary disease, or renal failure.
- No evidence of recurrent or metastatic disease via radiological or pathological in EMR in the 15 months prior to the baseline exercise assessment.
- Completion of all definitive primary adjuvant therapy (e.g., chemotherapy, radiotherapy, targeted therapy) at least 3 months prior to completion of historical exercise survey (i.e., at least 3 months prior to t-1) as part of MSK Cancer Survivorship Program standard intake. Adjuvant endocrine therapy is permitted.
試験中央連絡先
連絡先: Jessica Scott, PhD, 646-888-8093, [email protected]
連絡先: Chaya Moskowitz, PhD, 646-227-3607, [email protected]
4 1カ国の場所
California
City of Hope Cancer Center (Data Analysis Only), Duarte, California, 91010, United States
Lee Jones, PhD, 連絡先, 646-677-7440
募集未定
University of California, Los Angeles (Data or Specimen Analysis Only), Los Angeles, California, 90095-1781, United States
Paul Boutros, PhD, 連絡先, 310-794-7160
募集未定
New York
Weill Cornell Medical College (Data or Specimen Analysis Only), New York, New York, 10021, United States
Xiaoyue Ma, 連絡先, 646-962-8029
募集未定
Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York, 10065, United States
Jessica Scott, PhD, 連絡先, 646-888-8093
募集中