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El ensayo clínico NCT07030686 para Supervivencia, Recurrente, Recurrencia, CÁNCER, Remisión está reclutando. Consulte la vista de tarjeta del Radar de Ensayos Clínicos y las herramientas de descubrimiento de IA para conocer todos los detalles. O haga cualquier pregunta aquí.
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Association Between Exercise, Patient-Reported Outcomes, and Clinical Events in Adult Cancer Survivors

Reclutando
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El estudio clínico NCT07030686 es un ensayo observacional para Supervivencia, Recurrente, Recurrencia, CÁNCER, Remisión. Su estado actual es: reclutando. El ensayo se inició el 19 de marzo de 2020, con el objetivo de reclutar a 1000 participantes. Dirigido por el Centro Nacional del Cáncer, Japón, se espera que finalice el 19 de marzo de 2026. Los datos se actualizaron por última vez en ClinicalTrials.gov el 26 de noviembre de 2025.
Resumen
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.
Título oficial

Association Between Exercise, Patient-Reported Outcomes, and Clinical Events in Adult Cancer Survivors

Condiciones médicas
SupervivenciaRecurrenteRecurrenciaCÁNCERRemisión
Otros ID del ensayo
  • 20-101
Número del NCT
Inicio del ensayo (real)
2020-03-19
Última actualización
2025-11-26
Fecha de finalización (estimada)
2026-03-19
Inscripción (prevista)
1000
Tipo de estudio
Observacional
Estado general
Reclutando
Palabras clave
Survivorship
Exercise
cancer survivor
adult cancer survivor
no evidence of disease
20-101
Memorial Sloan Kettering Cancer Center
Brazos / Intervenciones
Grupo de participantesIntervención/Tratamiento
Arm 1: Usual Care
N/A
Arm 2: Exercise
Ejercicio
Exercise following completion of active treatment for the primary index cancer
Resultado primario
Medida de resultadoDescripción de la medidaPeriodo de tiempo
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
Criterios de elegibilidad

Criterios de edad
Adulto, Adulto mayor
Edad mínima
18 Years
Criterios de sexo
Todos
Admisión de voluntarios sanos

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.
Memorial Sloan Kettering Cancer Center logoCentro Nacional del Cáncer, Japón
Contactos centrales del ensayo
Contacto: Jessica Scott, PhD, 646-888-8093, [email protected]
Contacto: Chaya Moskowitz, PhD, 646-227-3607, [email protected]
4 Sitios del ensayo en 1 países

California

City of Hope Cancer Center (Data Analysis Only), Duarte, California, 91010, United States
Lee Jones, PhD, Contacto, 646-677-7440
Aún no recluta
University of California, Los Angeles (Data or Specimen Analysis Only), Los Angeles, California, 90095-1781, United States
Paul Boutros, PhD, Contacto, 310-794-7160
Aún no recluta

New York

Weill Cornell Medical College (Data or Specimen Analysis Only), New York, New York, 10021, United States
Xiaoyue Ma, Contacto, 646-962-8029
Aún no recluta
Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York, 10065, United States
Jessica Scott, PhD, Contacto, 646-888-8093
Reclutando