PROMIS-SF v2.0 -Cognitive Function 8a
BehavioralPatient-Reported Outcomes (PROs)
NCT Number: NCT05540782
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.
This study is active but is not currently recruiting participants.
Notify Me18 year and older
Male
Observational
Memorial Sloan Kettering Basking Ridge, Basking Ridge, New Jersey, United States
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patient-Reported Outcomes (PROs)
Time frame: 1 year
All participants will be evaluable as long as they have completed the PROMIS-SF v2.0 - Cognitive Function 8a.
Memorial Sloan Kettering Cancer Center
Other
Prostate Cancer Survivorship and Cognitive Health (PRO-HEALTH)
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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