Cognition in Older Breast Cancer Survivors: Treatment Exposure, APOE and Smoking History (NCT02122107)
๐ฉบ Plain-English Summary (8th-Grade Level)
In this study,the investigators are looking to see how older women who are survivors of breast cancer and either did or did not receive chemotherapy are affected by treatment, compared to older women who have never had cancer. Thinking and memory abilities normally decrease with age and the investigators want to see if the long-term effects of cancer treatments may make these problems worse. The investigators will also look at how thinking and memory abilities of older women are affected by genetics and smoking history. Genetics and other factors may affect the brain's chemicals or structure, and may either protect against the negative effects on thinking or make someone more at risk for them. MSK participants who previously consented to allostatic blood and saliva collection but have not yet provided any allostatic blood or saliva samples for this study, will not be asked to provide any further samples at follow-up. Participants who have consented to allostatic sample collection and provided one set of allostatic blood and saliva samples at a previous follow-up study visit will still be asked to provide a second set of samples at a later follow-up. COH participants will continue to provide allostatic blood and saliva collection as originally outlined
Who can join: Review the eligibility criteria below.
Location: City of Hope โ Duarte, California
Age range: 60 Years
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (2 Sites)
- City of Hope โ Duarte, California
- Memorial Sloan Kettering Cancer Center โ New York, New York
๐ Contact the Study Coordinator
Phone: (800) 826-4673
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ 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 ยง 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.
More studies in Breast Cancer Survivors
- Feasibility and Tolerability of Transcranial Direct Current Stimulation With Concurrent Cognitive Training โ New York, New York
- Improving Cognition After Cancer โ La Jolla, California
- Evaluation of an Online, Remote Cognitive Battery for Use in Cancer Survivorship โ New York, New York
- A Study of Attention and Memory Processes in Breast Cancer Survivors โ New York, New York
- taVNS for Breast Cancer Pain and Symptom Management โ Tallahassee, Florida
Explore by condition: All Breast Cancer Survivors clinical trials
๐ก 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.