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Clinical Trials/NCT05416996
NCT05416996
Active, not recruiting
Not Applicable

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

Memorial Sloan Kettering Cancer Center1 site in 1 country88 target enrollmentJune 5, 2022
ConditionsProstate Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
Memorial Sloan Kettering Cancer Center
Enrollment
88
Locations
1
Primary Endpoint
accrual number
Status
Active, not recruiting
Last Updated
11 months ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
June 5, 2022
End Date
June 2026
Last Updated
11 months ago
Study Type
Observational
Sex
Male

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 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

Exclusion Criteria

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

Outcomes

Primary Outcomes

accrual number

Time Frame: 1 year

patient satisfaction

Time Frame: 1 week

using MSK Engage portal survey

Secondary Outcomes

  • adherence to active surveillance(6 months)

Study Sites (1)

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