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De klinische studie NCT07030686 voor Overleving, Recidiverend, Recidief, KANKER, Remissie is recruterend. Bekijk de kaartweergave van de Klinische Studies Radar en de AI-ontdekkingstools voor alle details. Of stel hier een vraag.
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Kaartweergave

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

Recruterend
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De klinische studie NCT07030686 is een observationeel studie bij Overleving, Recidiverend, Recidief, KANKER, Remissie met de status recruterend. Het doel is om 1.000 deelnemers te includeren vanaf 19 maart 2020. De studie wordt geleid door Memorial Sloan Kettering Kankercentrum en de voltooiing is gepland op 19 maart 2026. Laatste update op ClinicalTrials.gov: 26 november 2025.
Beknopte samenvatting
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.
Officiële titel

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

Aandoeningen
OverlevingRecidiverendRecidiefKANKERRemissie
Andere studie-ID's
  • 20-101
NCT-ID
Startdatum (Werkelijk)
2020-03-19
Laatste update geplaatst
2025-11-26
Verwachte einddatum
2026-03-19
Inschrijving (Geschat)
1.000
Studietype
Observationeel
Status
Recruterend
Trefwoorden
Survivorship
Exercise
cancer survivor
adult cancer survivor
no evidence of disease
20-101
Memorial Sloan Kettering Cancer Center
Armen / Interventies
Deelnemersgroep/StudiearmInterventie/Behandeling
Arm 1: Usual Care
N.v.t.
Arm 2: Exercise
Oefening
Exercise following completion of active treatment for the primary index cancer
Primaire uitkomst
UitkomstmaatBeschrijving van de uitkomstmaatTijdsbestek
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
Geschiktheidscriteria

Leeftijd van deelnemers
Volwassene, Oudere volwassene
Minimumleeftijd
18 Years
Geslachten die in aanmerking komen voor de studie
Allen
Accepteert gezonde vrijwilligers
Ja

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 logoMemorial Sloan Kettering Kankercentrum
Centraal Contactpersoon
Contact: Jessica Scott, PhD, 646-888-8093, [email protected]
Contact: Chaya Moskowitz, PhD, 646-227-3607, [email protected]
4 Studielocaties in 1 landen

California

City of Hope Cancer Center (Data Analysis Only), Duarte, California, 91010, United States
Lee Jones, PhD, Contact, 646-677-7440
Nog niet rekruterend
University of California, Los Angeles (Data or Specimen Analysis Only), Los Angeles, California, 90095-1781, United States
Paul Boutros, PhD, Contact, 310-794-7160
Nog niet rekruterend

New York

Weill Cornell Medical College (Data or Specimen Analysis Only), New York, New York, 10021, United States
Xiaoyue Ma, Contact, 646-962-8029
Nog niet rekruterend
Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York, 10065, United States
Jessica Scott, PhD, Contact, 646-888-8093
Recruterend