Trial Radar AI
Clinical Trial NCT07030686 for Survivorship, Recurrent, Recurrence, Cancer, Remission is recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here.
One trial matched filter criteria
Card View

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

Recruiting
Clinical Trial NCT07030686 is an observational study for Survivorship, Recurrent, Recurrence, Cancer, Remission that is recruiting. It started on 19 March 2020 with plans to enroll 1,000 participants. Led by Memorial Sloan Kettering Cancer Center, it is expected to complete by 19 March 2026. The latest data from ClinicalTrials.gov was last updated on 26 November 2025.
Brief Summary
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.
Official Title

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

Conditions
SurvivorshipRecurrentRecurrenceCancerRemission
Other Study IDs
  • 20-101
NCT ID Number
Start Date (Actual)
2020-03-19
Last Update Posted
2025-11-26
Completion Date (Estimated)
2026-03-19
Enrollment (Estimated)
1,000
Study Type
Observational
Status
Recruiting
Keywords
Survivorship
Exercise
cancer survivor
adult cancer survivor
no evidence of disease
20-101
Memorial Sloan Kettering Cancer Center
Arms / Interventions
Participant Group/ArmIntervention/Treatment
Arm 1: Usual Care
N/A
Arm 2: Exercise
Exercise
Exercise following completion of active treatment for the primary index cancer
Primary Outcome Measures
Outcome MeasureMeasure DescriptionTime Frame
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
Eligibility Criteria

Eligible Ages
Adult, Older Adult
Minimum Age
18 Years
Eligible Sexes
All
Accepts Healthy Volunteers
Yes

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 Cancer Center
Study Central Contact
Contact: Jessica Scott, PhD, 646-888-8093, [email protected]
Contact: Chaya Moskowitz, PhD, 646-227-3607, [email protected]
4 Study Locations in 1 Countries

California

City of Hope Cancer Center (Data Analysis Only), Duarte, California, 91010, United States
Lee Jones, PhD, Contact, 646-677-7440
Not yet recruiting
University of California, Los Angeles (Data or Specimen Analysis Only), Los Angeles, California, 90095-1781, United States
Paul Boutros, PhD, Contact, 310-794-7160
Not yet recruiting

New York

Weill Cornell Medical College (Data or Specimen Analysis Only), New York, New York, 10021, United States
Xiaoyue Ma, Contact, 646-962-8029
Not yet recruiting
Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York, 10065, United States
Jessica Scott, PhD, Contact, 646-888-8093
Recruiting