Exercise Exposure Data Collection in Patients Undergoing Tumor Molecular Profiling (NCT03208374)
🩺 Plain-English Summary (8th-Grade Level)
This study will recruit approximately 5,000 patients with histologically confirmed cancer who have successfully completed MSK-IMPACT panel testing and collect information about tumor genetic results and patient exercise behavior history. The purpose of the study is to create a registry to collect exercise behavior history in patients who had IMPACT genetic panel testing on protocol IRB #12-245 "Genomic Profiling in Cancer Patients", IRB #06-107 "Storage and Research Use of Human Biospecimens," or IRB #09-141 "Collection of Human Biological Specimens from Patients for Research Studies." The investigators want to find a way to create an exercise database. This database will collect information about tumor genetic results and patient exercise behavior history.
Who can join: Review the eligibility criteria below.
Location: Memorial Sloan Kettering Basking Ridge (Consent only) — Basking Ridge, New Jersey
Age range: 18 Years
🧪 Interventions in This Study
- Prior Exercise Behavior Questions - Harvard Health Professionals Exercise Questionnaire (BEHAVIORAL)
- Current Exercise Behavior Questions: International Physical Activity Questionnaire Short Form (IPAQ SF) (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (7 Sites)
- Memorial Sloan Kettering Basking Ridge (Consent only) — Basking Ridge, New Jersey
- Memorial Sloan Kettering Monmouth (Consent only) — Middletown, New Jersey
- Memorial Sloan Kettering Bergen (Consent only) — Montvale, New Jersey
- Memorial Sloan Kettering Commack (Consent only) — Commack, New York
- Memorial Sloan Kettering Westchester (Consent only) — Harrison, New York
- Memorial Sloan Kettering Cancer Center — New York, New York
- Memorial Sloan Kettering Nassau (Consent only) — Uniondale, New York
📞 Contact the Study Coordinator
Phone: (800) 525-2225
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.