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Clinical Trial Summary

The purpose of this study is to collect information on how patients and their partners/close allies make treatment decisions when they have been diagnosed with early stage prostate cancer.


Clinical Trial Description

Each patient and his partner will fill out assessments at baseline. Thereafter we will obtain the patients' treatment decision (AT or AS) within approximately 6 months. Once a patient makes a decision, he and his partner will complete another set of questionnaires. The patient and his partner will then complete the remaining questionnaires approximately 6, 12, 18, and 24 months following the treatment decision. We will examine the associations between baseline assessments , and the treatment decision as well as the changes in the assessments and the treatment decision. We will also assess associations between follow-up assessments and the decision to change a treatment decision from AS to AT. Data from patients and partners/close allies will generally be analyzed separately, thus patients who do not have a partner (or partner declines to participate) can still be enrolled and their psychosocial outcomes assessed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01877070
Study type Observational
Source Memorial Sloan Kettering Cancer Center
Contact
Status Active, not recruiting
Phase
Start date June 2013
Completion date June 2025

See also
  Status Clinical Trial Phase
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Recruiting NCT03740191 - Spot-Scanning Based Hypofractionated Proton Therapy for Low and Intermediate Risk Prostate Cancer N/A
Terminated NCT03849365 - Study of Erectile Dysfunction, Urinary Incontinence and Related QoL After TOOKAD® VTP for Low Risk Prostate Cancer Phase 4
Recruiting NCT03088124 - Active Surveillance With or Without Apalutamide Treatment in Low Risk Prostate Cancer Phase 2