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临床试验 NCT07030686 针对生存期,复发性,复发,癌症,缓解目前招募中。请查看临床试验雷达卡片视图和 AI 发现工具了解所有详情,或在此提出任何问题。 | ||
一个试验符合筛选条件
卡片视图
Association Between Exercise, Patient-Reported Outcomes, and Clinical Events in Adult Cancer Survivors
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临床试验NCT07030686是一项针对生存期,复发性,复发,癌症,缓解的观察研究试验,目前试验状态为招募中。试验始于2020年3月19日,计划招募1,000名患者。该研究由纪念斯隆-凯特琳癌症中心主导,预计于2026年3月19日完成。试验数据来源于ClinicalTrials.gov,最后更新时间为2025年11月26日。
简要概括
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.
官方标题
Association Between Exercise, Patient-Reported Outcomes, and Clinical Events in Adult Cancer Survivors
疾病
生存期复发性复发癌症缓解其他研究标识符
- 20-101
NCT编号
实际开始日期
2020-03-19
最近更新发布
2025-11-26
预计完成日期
2026-03-19
计划入组人数
1,000
研究类型
观察研究
试验状态
招募中
关键词
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
试验组/干预措施
| 参与者组/试验组 | 干预措施/治疗方法 |
|---|---|
Arm 1: Usual Care | 不适用 |
Arm 2: Exercise | 锻炼 Exercise following completion of active treatment for the primary index cancer |
主要终点
| 结果指标 | 度量标准描述 | 时间框架 |
|---|---|---|
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 |
资格标准
适龄参与研究
成人, 老年人
最低年龄要求
18 Years
适龄性别
全部
接受健康志愿者
是
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.
研究中心联系人
联系人: Jessica Scott, PhD, 646-888-8093, [email protected]
联系人: Chaya Moskowitz, PhD, 646-227-3607, [email protected]
4 位于 1 个国家/地区的研究中心
California
City of Hope Cancer Center (Data Analysis Only), Duarte, California, 91010, United States
Lee Jones, PhD, 联系人, 646-677-7440
尚未招募
University of California, Los Angeles (Data or Specimen Analysis Only), Los Angeles, California, 90095-1781, United States
Paul Boutros, PhD, 联系人, 310-794-7160
尚未招募
New York
Weill Cornell Medical College (Data or Specimen Analysis Only), New York, New York, 10021, United States
Xiaoyue Ma, 联系人, 646-962-8029
尚未招募
Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York, 10065, United States
Jessica Scott, PhD, 联系人, 646-888-8093
招募中