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NCT05416996Active, not recruiting

A Study of Telemedicine Shared Medical Appointments (SMAs) Versus Individual Telemedicine Visits for People With Prostate Cancer

Feasibility Study of Randomizing Patients to Telemedicine Shared Medical Appointments Versus Telemedicine Single Visits for Men With Prostate Cancer on Active Surveillance

Source: ClinicalTrials.gov · Last updated 21 Jul 2026

Brief summary (registry, in English)

The purpose of this study is to see if a telemedicine group doctor's appointment is a practical (feasible) and acceptable method for following people with prostate cancer being managed with active surveillance when compared with the usual approach of individual telemedicine visits, which involve the participant visiting a doctor on their own. The researchers will compare the telemedicine group and individual visits by measuring on participant satisfaction and quality of life in each type of visit. Telemedicine is the use of secure video technology on a desktop computer, laptop, smartphone, or tablet to provide and receive healthcare from a distance.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
88 (actual)
First submitted
7 Jun 2022
Start date
5 Jun 2022
Primary completion date
Jun 2027
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT05416996

What you commit to

  • Study type: Observational
  • Participants enrolled: 88
  • From 5 Jun 2022 to the primary completion date, Jun 2027
  • 1 site 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, not your situation.

Who cannot take part

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

Other

  • Plan to undergo a prostate biopsy at this follow-up visit

Who the study is looking for

  • A scheduled appointment for a subsequent Active Surveillance (AS) follow-up visit for management of localized prostate cancer
  • Biopsy Gleason score 3+3=6 (Grade Group 1) or biopsy Gleason score 3+4=7 (Grade Group 2)
  • Clinical T stage ≤T2B
  • Access to a device with Zoom
  • Ability to speak and understand English

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite 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.