跳至主要内容
临床试验/NCT03996239
NCT03996239进行中(未招募)不适用

Exercise as Interception Therapy: A "Proof-of-Concept" Digitized Trail

Memorial Sloan Kettering Cancer Center10 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2019年6月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
38
试验地点
10
主要终点
number of patients with variant allele frequency (VAF)

研究概览

简要总结

This study is being done to answer the following question: Will aerobic exercise (exercise that stimulates and strengthens the heart and lungs, and improves the body's use of oxygen) change the biomarkers (signs of disease) found in the blood?

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

盲法说明

For cohort 3 only. Men with histologically-confirmed localized prostate cancer undergoing active surveillance. Both patients and investigators will be fully blinded to the ctDNA status of patients during study participation.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Cohort 1: CH
  • •CH called by MSK practices as documented by an MSK physician
  • •Age ≥18 yrs
  • •Completion of all anticancer therapy
  • •High risk of cardiovascular disease defined by presence of at least one of the following:
  • •Prior treatment with chemotherapy
  • •Prior left-sided breast and/or chest wall radiotherapy
  • •Currently receiving or previously received androgen deprivation therapy Prior bone marrow transplant
  • •History of smoking
  • •Currently treated for one or more cardiovascular risk factors (i.e., hypertension, diabetes, hyperlipidemia)
  • •Performing less than 150 minutes of structured moderate-intensity or strenuous-intensity exercise per week, as evaluated by self-report
  • •Willingness to comply with all study-related procedures
  • •Cohort 2: Solid Tumor
  • •Patients at risk of harboring circulating tumor DNA as defined by one of the following:
  • •Histologically confirmed stage III (i.e., high risk of recurrence) colorectal cancer within 2 years of completion of all adjuvant therapy.
  • •Histologically confirmed stage III breast cancer with residual disease after neoadjuvant therapy and within 12 months of completing (neo)adjuvant chemotherapy
  • •Patients with metastatic breast cancer and radiographic stable disease or NED for ≥6 months and not currently receiving chemotherapy (endocrine therapy and anti-HER2 antibodies allowed)
  • •Age ≥ 18 yrs
  • •Performing less than 150 minutes of structured moderate-intensity or strenuous-intensity exercise per week, as evaluated by self-report
  • •Willingness to comply with all study-related procedures
  • •Cohort 3: Active Surveillance
  • •Men with histologically confirmed localized prostate cancer undergoing active surveillance
  • •Age ≥ 18 yrs
  • •Performing less than 15 minutes of structured moderate-intensity or strenuous-intensity exercise per week, as evaluated by self-report
  • •Willingness to comply with all study-related procedures
  • •Cleared for exercise participation as per pre-screening clearance via PAR-Q+
  • •Cohort 4: Lynch Syndrome
  • •Age ≥18 yrs
  • •Hereditary colorectal cancer syndrome, specifically Lynch syndrome, defined by the presence of a deleterious germline mutation in the MLH1, MSH2, MSH6, PMS2 or EPCAM genes
  • •Have a portion of the distal colon or rectosigmoid intact to enable collection of normal mucosa biopsies
  • •Performing less than 150 minutes of structured moderate-intensity or strenuous-intensity exercise per week, as evaluated by self-report
  • •Willingness to comply with all study-related procedures
  • •Cleared for exercise participation as per pre-screening clearance via PAR-Q+
  • •Cohort 5: EDD Phase 0a
  • •Age ≥18 yrs
  • •Receiving investigational agent under an EDD protocol for at least 2 months.
  • •Performing less than 150 minutes of structured moderate-intensity or strenuous-intensity exercise per week, as evaluated by self-report
  • •Willingness to comply with all study-related procedures
  • •Cleared for exercise participation as per pre-screening clearance via PAR-Q+
  • •Age ≥18 yrs
  • •Newly Within 3 months of initiating investigational agent on an EDD Service protocol
  • •Performing less than 150 minutes of structured moderate-intensity or strenuous-intensity exercise per week, as evaluated by self-report
  • •Willingness to comply with all study-related procedures
  • •Cleared for exercise participation as per pre-screening clearance via PAR-Q+

排除标准

  • •Concurrent use of any form of antitumor therapy (endocrine therapy and anti-HER2 antibodies allowed)
  • •Enrollment onto any other interventional investigational study except interventions determined by the PI not to confound study outcomes (does not apply to Cohort 5: EDD)
  • •Any other condition or intercurrent illness that, in the opinion of the investigator, makes the subject a poor candidate for study participation.
  • •Mental impairment leading to inability to cooperate
  • •Any of the following contraindications to cardiopulmonary exercise testing (Cohorts 1 and 2 only):
  • •Acute myocardial infarction within 3-5 days of any planned study procedures;
  • •Unstable angina
  • •Uncontrolled arrhythmia causing symptoms or hemodynamic compromise
  • •Recurrent syncope
  • •Active endocarditis
  • •Acute myocarditis or pericarditis
  • •Symptomatic severe aortic stenosis
  • •Uncontrolled heart failure
  • •Acute pulmonary embolus or pulmonary infarction within 3 months of any planned study procedures
  • •Thrombosis of lower extremities within 3 months of any planned study procedures
  • •Suspected dissecting aneurysm
  • •Uncontrolled asthma
  • •Pulmonary edema
  • •Respiratory failure
  • •Acute non-cardiopulmonary disorders that may affect exercise performance
  • •Room air desaturation at rest ≤ 85% (Cohorts 1 and 2 only)

研究组 & 干预措施

Individuals enrolled on Early Drug Development (EDD) trials

Experimental

Participants will receive structured exercise therapy for 24 weeks. Participants will be followed by standard of care clinical follow-up

干预措施: exercise (walking) (Behavioral)

patients with clonal hematopoiesis

Experimental

Exercise treatment will consist of individualized walking delivered up to 5 times weekly. Patients in all cohorts will receive one dose of exercise (i.e., ~300 mins/wk following a non-linear dosing schedule) in both cohorts. Patients will have the option to receive exercise treatment at MSK or at their residence. Home-based exercise will be implemented and monitored using a telemedicine approach (i.e.,TeleEx) established in the Exercise-Oncology (ExOnc) Service

干预措施: exercise (walking) (Behavioral)

Individuals with Lynch Syndrome

Experimental

Exercise treatment will consist of individualized walking delivered up to 5 times weekly. Patients in all cohorts will receive one dose of exercise (i.e., ~300 mins/wk following a non-linear dosing schedule) in both cohorts. Patients will have the option to receive exercise treatment at MSK or at their residence. Home-based exercise will be implemented and monitored using a telemedicine approach (i.e.,TeleEx) established in the Exercise-Oncology (ExOnc) Service

干预措施: exercise (walking) (Behavioral)

Individuals with Lynch Syndrome

Experimental

Exercise treatment will consist of individualized walking delivered up to 5 times weekly. Patients in all cohorts will receive one dose of exercise (i.e., ~300 mins/wk following a non-linear dosing schedule) in both cohorts. Patients will have the option to receive exercise treatment at MSK or at their residence. Home-based exercise will be implemented and monitored using a telemedicine approach (i.e.,TeleEx) established in the Exercise-Oncology (ExOnc) Service

干预措施: plasma samples (Other)

Individuals with Lynch Syndrome

Experimental

Exercise treatment will consist of individualized walking delivered up to 5 times weekly. Patients in all cohorts will receive one dose of exercise (i.e., ~300 mins/wk following a non-linear dosing schedule) in both cohorts. Patients will have the option to receive exercise treatment at MSK or at their residence. Home-based exercise will be implemented and monitored using a telemedicine approach (i.e.,TeleEx) established in the Exercise-Oncology (ExOnc) Service

干预措施: blood draw (Other)

patients with clonal hematopoiesis

Experimental

Exercise treatment will consist of individualized walking delivered up to 5 times weekly. Patients in all cohorts will receive one dose of exercise (i.e., ~300 mins/wk following a non-linear dosing schedule) in both cohorts. Patients will have the option to receive exercise treatment at MSK or at their residence. Home-based exercise will be implemented and monitored using a telemedicine approach (i.e.,TeleEx) established in the Exercise-Oncology (ExOnc) Service

干预措施: blood draw (Other)

post treatment patients with breast or colorectal cancer

Experimental

Exercise treatment will consist of individualized walking delivered up to 5 times weekly. Patients in all cohorts will receive one dose of exercise (i.e., ~300 mins/wk following a non-linear dosing schedule) in both cohorts. Patients will have the option to receive exercise treatment at MSK or at their residence. Home-based exercise will be implemented and monitored using a telemedicine approach (i.e.,TeleEx) established in the Exercise-Oncology (ExOnc) Service

干预措施: exercise (walking) (Behavioral)

post treatment patients with breast or colorectal cancer

Experimental

Exercise treatment will consist of individualized walking delivered up to 5 times weekly. Patients in all cohorts will receive one dose of exercise (i.e., ~300 mins/wk following a non-linear dosing schedule) in both cohorts. Patients will have the option to receive exercise treatment at MSK or at their residence. Home-based exercise will be implemented and monitored using a telemedicine approach (i.e.,TeleEx) established in the Exercise-Oncology (ExOnc) Service

干预措施: plasma samples (Other)

post treatment patients with breast or colorectal cancer

Experimental

Exercise treatment will consist of individualized walking delivered up to 5 times weekly. Patients in all cohorts will receive one dose of exercise (i.e., ~300 mins/wk following a non-linear dosing schedule) in both cohorts. Patients will have the option to receive exercise treatment at MSK or at their residence. Home-based exercise will be implemented and monitored using a telemedicine approach (i.e.,TeleEx) established in the Exercise-Oncology (ExOnc) Service

干预措施: blood draw (Other)

men with localized prostate cancer undergoing active surveillance

Experimental

Exercise treatment will consist of individualized walking delivered up to 5 times weekly. Patients in all cohorts will receive one dose of exercise (i.e., ~300 mins/wk following a non-linear dosing schedule) in both cohorts. Patients will have the option to receive exercise treatment at MSK or at their residence. Home-based exercise will be implemented and monitored using a telemedicine approach (i.e.,TeleEx) established in the Exercise-Oncology (ExOnc) Service

干预措施: exercise (walking) (Behavioral)

men with localized prostate cancer undergoing active surveillance

Experimental

Exercise treatment will consist of individualized walking delivered up to 5 times weekly. Patients in all cohorts will receive one dose of exercise (i.e., ~300 mins/wk following a non-linear dosing schedule) in both cohorts. Patients will have the option to receive exercise treatment at MSK or at their residence. Home-based exercise will be implemented and monitored using a telemedicine approach (i.e.,TeleEx) established in the Exercise-Oncology (ExOnc) Service

干预措施: plasma samples (Other)

men with localized prostate cancer undergoing active surveillance

Experimental

Exercise treatment will consist of individualized walking delivered up to 5 times weekly. Patients in all cohorts will receive one dose of exercise (i.e., ~300 mins/wk following a non-linear dosing schedule) in both cohorts. Patients will have the option to receive exercise treatment at MSK or at their residence. Home-based exercise will be implemented and monitored using a telemedicine approach (i.e.,TeleEx) established in the Exercise-Oncology (ExOnc) Service

干预措施: blood draw (Other)

结局指标

主要结局

number of patients with variant allele frequency (VAF)

时间窗: 2 years

measured by targeted CH panel in peripheral blood

changes in residual tumor burden (Solid tumor group)

时间窗: 2 years

measured by the amount of circulating tumor DNA (ctDNA)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (10)

Loading locations...

相似试验