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Clinical Trials/NCT04136340
NCT04136340
Completed
N/A

Virtual Visits by Supportive Care Specialists to Cancer Patients at Home: A Randomized Controlled Pilot Noninferiority Trial of Video Telemedicine

Memorial Sloan Kettering Cancer Center1 site in 1 country33 target enrollmentOctober 24, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Cancer
Sponsor
Memorial Sloan Kettering Cancer Center
Enrollment
33
Locations
1
Primary Endpoint
Health-Related Quality of Life: FACT-G
Status
Completed
Last Updated
9 months ago

Overview

Brief Summary

This study will test whether supportive care follow-up delivered to cancer patients at home by telemedicine ("virtual" medical visits using telecommunications technologies) is as effective as in-person supportive care visits in the clinic.

Detailed Description

The protocol was developed and initially implemented when the standard of care for Supportive Care (and oncology) follow-up at MSK was in-person visiting and home telemedicine was only in an early stage of use at the institution. During the COVID-19 crisis, all outpatient Supportive Care visits and most oncology visits at MSK have been handled via telemedicine to protect patient (and staff) safety.

Registry
clinicaltrials.gov
Start Date
October 24, 2019
End Date
July 3, 2025
Last Updated
9 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • age 18 years or older
  • solid tumor of any type
  • completed an initial in-person clinic visit (i.e. an IR/NV or AFX visit) at Rockefeller Outpatient Pavilion with Dr. Saldivar, Dr. Martin, Supportive Care physicians, or Andrea Dolan, a Supportive Care nurse practitioner
  • planned for Supportive Care Service follow-up visits, but none yet completed
  • enrolled on the MyMSK secure online patient portal and have access to the portal off site of MSK campuses
  • resident of New York or New Jersey or Connecticut (clinicians may not be licensed in other states, as would be required for televisits to patients there)

Exclusion Criteria

  • Patients and informal caregivers who cannot communicate with clinicians/respond to instruments in English without the use of an interpreter

Outcomes

Primary Outcomes

Health-Related Quality of Life: FACT-G

Time Frame: Week 14

will be used to quantify health-related quality of life at baseline and Week 14 after randomization. All items in the FACT-G use a 5-point scale (0=Not at all to 4=Very much) and the total score sums four subscales and ranges from 0-108 (higher=better QoL). Change in total score at Week 14 after randomization vs. baseline.

Study Sites (1)

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