Trial Radar KI | ||
|---|---|---|
enums.trial_summary.trial_summary_welcome | ||
Eine Studie entspricht den Filterkriterien
Kartenansicht
Association Between Exercise, Patient-Reported Outcomes, and Clinical Events in Adult Cancer Survivors
Die Details der klinischen Studie sind hauptsächlich auf Englisch verfügbar. Trial Radar KI kann jedoch helfen! Klicken Sie einfach auf 'Studie erklären', um die Informationen zur Studie in der ausgewählten Sprache anzuzeigen und zu besprechen.
Die klinische Studie NCT07030686 ist eine beobachtungsstudie zur Untersuchung von Überlebenszeit, Rezidivierend, Rezidiv, KREBS, Remission und hat den Status offene rekrutierung. Die Studie startete am 19. März 2020 und soll 1.000 Teilnehmer aufnehmen. Durchgeführt von Memorial Sloan Kettering Krebszentrum ist der Abschluss für 19. März 2026 geplant. Die Daten von ClinicalTrials.gov wurden zuletzt am 26. November 2025 aktualisiert.
Kurzbeschreibung
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.
Offizieller Titel
Association Between Exercise, Patient-Reported Outcomes, and Clinical Events in Adult Cancer Survivors
Erkrankungen
ÜberlebenszeitRezidivierendRezidivKREBSRemissionWeitere Studien-IDs
- 20-101
NCT-Nummer
Studienbeginn (tatsächlich)
2020-03-19
Zuletzt aktualisiert
2025-11-26
Studienende (vorauss.)
2026-03-19
Geplante Rekrutierung
1.000
Studientyp
Beobachtungsstudie
Status
Offene Rekrutierung
Stichwörter
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
Studienarme/Interventionen
| Teilnehmergruppe/Studienarm | Intervention/Behandlung |
|---|---|
Arm 1: Usual Care | Nicht zutreffend |
Arm 2: Exercise | Übung Exercise following completion of active treatment for the primary index cancer |
Hauptergebnismessungen
| Ergebnismessung | Beschreibung der Messung | Zeitrahmen |
|---|---|---|
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 |
Eignungskriterien
Zugelassene Altersgruppen
Erwachsene, Ältere Erwachsene
Mindestalter
18 Years
Zugelassene Geschlechter
Alle
Akzeptiert gesunde Freiwillige
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.
Zentrale Studienkontakte
Kontakt: Jessica Scott, PhD, 646-888-8093, [email protected]
Kontakt: Chaya Moskowitz, PhD, 646-227-3607, [email protected]
4 Studienstandorte in 1 Ländern
California
City of Hope Cancer Center (Data Analysis Only), Duarte, California, 91010, United States
Lee Jones, PhD, Kontakt, 646-677-7440
Noch nicht rekrutierend
University of California, Los Angeles (Data or Specimen Analysis Only), Los Angeles, California, 90095-1781, United States
Paul Boutros, PhD, Kontakt, 310-794-7160
Noch nicht rekrutierend
New York
Weill Cornell Medical College (Data or Specimen Analysis Only), New York, New York, 10021, United States
Xiaoyue Ma, Kontakt, 646-962-8029
Noch nicht rekrutierend
Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York, 10065, United States
Jessica Scott, PhD, Kontakt, 646-888-8093
Offene Rekrutierung