임상 레이더 AI | ||
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임상시험 NCT07030686은(는) 생존자 상태, 재발성, 재발, 암, 관해에 대해 모집중 상태입니다. 모든 세부 정보를 보려면 임상시험 레이더 카드 뷰와 AI 발견 도구를 확인하거나 여기에서 무엇이든 물어보세요. | ||
하나의 임상시험이 필터 기준과 일치합니다.
카드 뷰
Association Between Exercise, Patient-Reported Outcomes, and Clinical Events in Adult Cancer Survivors
임상시험 세부 정보는 주로 영어로 제공됩니다. 하지만 임상 레이더 AI가 도와드릴 수 있습니다! '시험 설명하기'를 클릭하여 선택한 언어로 임상시험 정보를 확인하고, 이에 대해 AI와 논의해 보세요.
임상시험 NCT07030686은(는) 생존자 상태, 재발성, 재발, 암, 관해에 대해 알아보는 관찰연구입니다. 현재 상태는 모집중이며, 연구는 2020년 3월 19일에 시작되어 1,000명의 참여자를 모집하고 있습니다. 메모리얼 슬론 케터링 암센터이(가) 진행하며, 2026년 3월 19일까지 완료될 예정입니다. ClinicalTrials.gov의 가장 최근 정보는 2025년 11월 26일에 갱신되었습니다.
간단한 개요
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.
공식 제목
Association Between Exercise, Patient-Reported Outcomes, and Clinical Events in Adult Cancer Survivors
질환/상태
생존자 상태재발성재발암관해기타 연구 식별자
- 20-101
NCT 번호
실제 연구 시작일
2020-03-19
최신 업데이트 게시
2025-11-26
예상 연구 완료일
2026-03-19
계획된 등록 인원
1,000
연구종류
관찰연구
상태
모집중
키워드
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
시험군 / 개입
| 참가자 그룹/시험군 | 개입/치료 |
|---|---|
Arm 1: Usual Care | 해당 없음 |
Arm 2: Exercise | 운동 Exercise following completion of active treatment for the primary index cancer |
주요결과변수
| 결과변수 | 측정값 설명 | 시간 범위 |
|---|---|---|
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 |
적격성 기준
연령대
성인, 노인
최소 연령
18 Years
참여 가능한 성별
전체
건강한 참가자 허용
네
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.
연구 대표 연락처
연락처: Jessica Scott, PhD, 646-888-8093, [email protected]
연락처: Chaya Moskowitz, PhD, 646-227-3607, [email protected]
4 1개국에 임상시험 장소
California
City of Hope Cancer Center (Data Analysis Only), Duarte, California, 91010, United States
Lee Jones, PhD, 연락처, 646-677-7440
대상자모집전
University of California, Los Angeles (Data or Specimen Analysis Only), Los Angeles, California, 90095-1781, United States
Paul Boutros, PhD, 연락처, 310-794-7160
대상자모집전
New York
Weill Cornell Medical College (Data or Specimen Analysis Only), New York, New York, 10021, United States
Xiaoyue Ma, 연락처, 646-962-8029
대상자모집전
Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York, 10065, United States
Jessica Scott, PhD, 연락처, 646-888-8093
모집중