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NCT01877070Active, not recruiting

Decision Making in Men With Early Stage Prostate Cancer Patients and Partners/Close Allies

Source: ClinicalTrials.gov · Last updated 2 Jul 2026

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
541 (estimated)
First submitted
11 Jun 2013
Start date
Jun 2013
Primary completion date
Jun 2027
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT01877070

What you commit to

  • Study type: Observational
  • Planned participants: 541
  • From Jun 2013 to the primary completion date, Jun 2027
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of a cancer other than prostate cancer and non-melanoma skin cancer
  • Significant psychiatric or cognitive disturbance sufficient, in the investigator's judgment, to preclude providing informed consent or participating in the study activities (i.e., acute psychiatric symptoms which require individual treatment)
    • For partners/close allies:
  • Significant psychiatric or cognitive disturbance sufficient, in the investigator's judgment, to preclude providing informed consent or participating in the study activities (i.e., acute psychiatric symptoms which require individual treatment)

Other

  • For patients:

Who the study is looking for

  • For patients:
  • Men who meet the NCCN guidelines for low risk prostate cancer, which include all of the following:
    • Most recent Gleason score ≤ 6, or clinical stage T1a or less;
    • Most recent PSA level below 10;
    • In the most recent biopsy, had fewer than 3 positive biopsy cores (with ≤ 50% cancer in each); OR the patient's doctor discussed active surveillance as a treatment option (as documented in visit notes of the patient's medical record)
  • Are able to speak, read, write and understand English well enough to provide informed consent and complete study tasks
  • Has not made a treatment decision prior to consent, as per self report
  • 18 years of age or older
    • For partners/close allies:
  • Considered a partner/close ally to the patient in the treatment making decision, as reported by the patient
  • Are able to speak, read, write and understand English well enough to provide informed consent and complete study tasks
  • 18 years old or older

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Memorial Sloan Kettering Westchester
Coordinator of this site? Confirm its status
HarrisonUnited StatesUnknown status
Mount Sinai Hospital
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.