A Study of Cognitive Health in Survivors of Prostate Cancer

  • End date
    Sep 8, 2024
  • participants needed
  • sponsor
    Memorial Sloan Kettering Cancer Center
Updated on 3 April 2023


The purpose of this study is to collect information that may help the researchers understand the relationship between prostate cancer survivors' experiences of cancer-related cognitive dysfunction (CRCD) and their other conditions (co-morbid factors), including anxiety, depression, and insomnia. The researchers will also find out how additional things may contribute to CRCD, including social factors, the characteristics of participants' prostate cancer, and the type of cancer treatment or other medications they received.

Condition Prostate Cancer, Survivorship
Treatment PROMIS-SF v2.0 -Cognitive Function 8a
Clinical Study IdentifierNCT05540782
SponsorMemorial Sloan Kettering Cancer Center
Last Modified on3 April 2023


Yes No Not Sure

Inclusion Criteria

Age 18 years or older
History of histologically documented PC of any stage
No evidence of PC Disease

Exclusion Criteria

<1 month since completion of surgery, radiation, chemotherapy, or ADT
Diagnosis of Alzheimer's disease, vascular dementia, Parkinson disease, or other organic brain disorder
Score >10 indicative of dementia on Blessed Orientation Memory Concentration
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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