Trial Radar IA | ||
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Lo studio clinico NCT07030686 per Sopravvivenza, Recidivante, Recidiva, CANCRO, Remissione è in arruolamento. Consulti la vista a schede del Radar degli Studi Clinici e gli strumenti di scoperta IA per tutti i dettagli. Oppure, ponga pure una domanda qui. | ||
Un studio corrisponde ai criteri del filtro
Vista a schede
Association Between Exercise, Patient-Reported Outcomes, and Clinical Events in Adult Cancer Survivors
I dettagli dello studio clinico sono disponibili principalmente in inglese. Tuttavia, Trial Radar IA può essere d'aiuto! Basta cliccare su 'Spiega lo studio' per visualizzare e discutere le informazioni sullo studio nella lingua selezionata.
La sperimentazione clinica NCT07030686 è uno studio osservazionale per Sopravvivenza, Recidivante, Recidiva, CANCRO, Remissione, attualmente in arruolamento. Avviato il 19 marzo 2020, prevede di arruolare 1.000 partecipanti. Sotto la guida di il Centro oncologico Memorial Sloan Kettering, dovrebbe concludersi entro il 19 marzo 2026. I dati più recenti da ClinicalTrials.gov sono stati aggiornati l'ultima volta il 26 novembre 2025.
Sommario breve
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.
Titolo ufficiale
Association Between Exercise, Patient-Reported Outcomes, and Clinical Events in Adult Cancer Survivors
Condizioni
SopravvivenzaRecidivanteRecidivaCANCRORemissioneAltri ID dello studio
- 20-101
Numero NCT
Data di inizio (effettiva)
2020-03-19
Ultimo aggiornamento pubblicato
2025-11-26
Data di completamento (stimata)
2026-03-19
Arruolamento (previsto)
1.000
Tipo di studio
Osservazionale
Stato
In arruolamento
Parole chiave
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
Bracci / Interventi
| Gruppo/Braccio di partecipanti | Intervento/Trattamento |
|---|---|
Arm 1: Usual Care | N.D. |
Arm 2: Exercise | Esercizio Exercise following completion of active treatment for the primary index cancer |
Esito primario
| Misure di esito | Descrizione della misura | Arco temporale |
|---|---|---|
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 |
Criteri di eleggibilità
Età idonea
Adulto, Adulto anziano
Età minima
18 Years
Sessi idonei
Tutti
Accetta volontari sani
Sì
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.
Contatti principali dello studio
Contatto: Jessica Scott, PhD, 646-888-8093, [email protected]
Contatto: Chaya Moskowitz, PhD, 646-227-3607, [email protected]
4 Centri dello studio in 1 paesi
California
City of Hope Cancer Center (Data Analysis Only), Duarte, California, 91010, United States
Lee Jones, PhD, Contatto, 646-677-7440
Non ancora in arruolamento
University of California, Los Angeles (Data or Specimen Analysis Only), Los Angeles, California, 90095-1781, United States
Paul Boutros, PhD, Contatto, 310-794-7160
Non ancora in arruolamento
New York
Weill Cornell Medical College (Data or Specimen Analysis Only), New York, New York, 10021, United States
Xiaoyue Ma, Contatto, 646-962-8029
Non ancora in arruolamento
Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York, 10065, United States
Jessica Scott, PhD, Contatto, 646-888-8093
In arruolamento