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L'essai clinique NCT07030686 pour Survie, Récurrent, Récidive, CANCER, Rémission est en recrutement. Consultez la vue en carte du Radar des Essais Cliniques et les outils de découverte par IA pour tous les détails, ou posez vos questions ici. | ||
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Vue en carte
Association Between Exercise, Patient-Reported Outcomes, and Clinical Events in Adult Cancer Survivors
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L'étude clinique NCT07030686 est un essai observationnel pour Survie, Récurrent, Récidive, CANCER, Rémission. Son statut actuel est : en recrutement. L'étude a débuté le 19 mars 2020 et vise à recruter 1 000 participants. Dirigé par le Centre de cancérologie Memorial Sloan Kettering, l'essai devrait être terminé d'ici le 19 mars 2026. Les données du site ClinicalTrials.gov ont été mises à jour pour la dernière fois le 26 novembre 2025.
Résumé succinct
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.
Titre officiel
Association Between Exercise, Patient-Reported Outcomes, and Clinical Events in Adult Cancer Survivors
Conditions
SurvieRécurrentRécidiveCANCERRémissionAutres identifiants de l'essai
- 20-101
Numéro NCT
Date de début (réel)
2020-03-19
Dernière mise à jour publiée
2025-11-26
Date de fin (estimée)
2026-03-19
Inscription (estimée)
1 000
Type d'essai
Observationnel
Statut
En recrutement
Mots clés
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
Bras / Interventions
| Groupe de participants/Bras | Intervention/Traitement |
|---|---|
Arm 1: Usual Care | N/A |
Arm 2: Exercise | EXERCICE Exercise following completion of active treatment for the primary index cancer |
Critère principal d'évaluation
| Critères d'évaluation | Description de critères | Période |
|---|---|---|
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 |
Critères d'éligibilité
Âges éligibles
Adulte, Adulte âgé
Âge minimum
18 Years
Sexes éligibles
Tous
Accepte les volontaires en bonne santé
Oui
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.
Contact central de l'essai
Contact: Jessica Scott, PhD, 646-888-8093, [email protected]
Contact: Chaya Moskowitz, PhD, 646-227-3607, [email protected]
4 Centres de l'essai dans 1 pays
California
City of Hope Cancer Center (Data Analysis Only), Duarte, California, 91010, United States
Lee Jones, PhD, Contact, 646-677-7440
Pas encore en recrutement
University of California, Los Angeles (Data or Specimen Analysis Only), Los Angeles, California, 90095-1781, United States
Paul Boutros, PhD, Contact, 310-794-7160
Pas encore en recrutement
New York
Weill Cornell Medical College (Data or Specimen Analysis Only), New York, New York, 10021, United States
Xiaoyue Ma, Contact, 646-962-8029
Pas encore en recrutement
Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York, 10065, United States
Jessica Scott, PhD, Contact, 646-888-8093
En recrutement