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
- Diseases
- Prostate cancer
- 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
Sites (3)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Memorial Sloan Kettering Westchester Coordinator of this site? Confirm its status | Harrison | United States | Unknown status |
| Mount Sinai Hospital Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Memorial Sloan-Kettering Cancer Center Coordinator of this site? Confirm its status | New York | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.