CClinicalTrials.gg
RecruitingNCT06954337Updated Jul 31, 2026

MATCH-UP: MAking Telehealth-Delivery of Cancer Care at Home Effective and Safe-Upscaled: A Pragmatic Cluster Randomized Trial

An interventional study of Usual practice pattern (UPP) and Experimental: Enhanced Telehealth (ET) in Breast Cancer and Prostate Cancer, sponsored by Memorial Sloan Kettering Cancer Center. Recruiting at 7 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-31.

Sponsored by Memorial Sloan Kettering Cancer Center · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Started May 2025; still recruiting 1 year 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
1,750
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

Many people with cancer spend a lot of time and money traveling to and from the doctor's office for cancer care. MSK's goal is to make getting cancer care easier by cutting down the need to make in-person visits to MSK. MSK is trying to do this through a new option called enhanced telehealth.

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Conditions studied

  • Breast Cancer
  • Prostate Cancer

Keywords

  • Telehealth
  • Cancer Care at Home
  • 25-055
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In context

Breast Neoplasms

12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

This study's planned enrollment of 1,750 is above the median of 72 across 9,302 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Memorial Sloan Kettering Cancer Center is the lead sponsor of 1,930 studies on the registry; 328 are open to participants now.

Of its 129 completed or terminated interventional studies of FDA-regulated products, 66 (51%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients with breast or prostate cancer at Memorial Sloan Kettering Cancer Center who have had at least 3 prior medical oncology visits.

Exclusion criteria

Exclusion Criteria:

  • Patient is enrolled on a therapeutic clinical trial.
  • Patients whose primary language is not currently supported by Epic.
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Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
1,750 participants (estimated)

Study arms

  • Active comparator
    Usual practice pattern (UPP)

    Usual practice pattern (UPP) of patient's medical oncologist

    Other: Usual practice pattern (UPP) · Other: Experimental: Enhanced Telehealth (ET)

  • Experimental
    Enhanced Telehealth (ET)

    Enhanced Telehealth (ET) practice pattern of patient's medical oncologist

    Other: Usual practice pattern (UPP) · Other: Experimental: Enhanced Telehealth (ET)

Interventions

  • OtherUsual practice pattern (UPP)

    Patient follows usual practice pattern for routine care

  • OtherExperimental: Enhanced Telehealth (ET)

    Patient follows enhanced telehealth practice pattern. As clinically appropriate, patients given option to shift routine care from face-to-face to at-home services available at institution: telehealth visits, home phlebotomy, and educational support for home administration of injection medications

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What researchers measure

Primary outcomes

  1. Proportion of routine face to face medical oncology related visits out of total medical oncology related visits

    all patients who meet eligibility criteria and have completed at least 2 medical oncology visits during the 12 month follow up period will be included for endpoint evaluability during analyses

    Time frame: 12 months

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Study locations

7 of 7 sites recruiting
  • Memorial Sloan Kettering Basking Ridge (All Protocol Activities)
    Basking Ridge, New Jersey 07920, United States
    • Erin Bange, MD, MSCE · Contact · 646-422-4680
    Recruiting
  • Memorial Sloan Kettering Monmouth (All Protocol Activities)
    Middletown, New Jersey 07748, United States
    • Erin Bange, MD, MSCE · Contact · 646-422-4680
    Recruiting
  • Memorial Sloan Kettering Bergen (All Protocol Activities)
    Montvale, New Jersey 07645, United States
    • Erin Bange, MD, MSCE · Contact · 646-422-4680
    Recruiting
  • Memorial Sloan Kettering Suffolk - Commack (All Protocol Activities)
    Commack, New York 11725, United States
    • Erin Bange, MD, MSCE · Contact · 646-422-4680
    Recruiting
  • Memorial Sloan Kettering Westchester (All Protocol Activities)
    Harrison, New York 10604, United States
    • Erin Bange, MD, MSCE · Contact · 646-422-4680
    Recruiting
  • Memorial Sloan Kettering Cancer Center (All Protocol Activites)
    New York, New York 10065, United States
    • Erin Bange, MD, MSCE · Contact · 646-422-4680
    Recruiting
  • Memorial Sloan Kettering Nassau (All Protocol Activities)
    Uniondale, New York 11553, United States
    • Erin Bange, MD, MSCE · Contact · 646-422-4680
    Recruiting
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References and documents

Individual participant data

Plan to share: Yes — Memorial Sloan Kettering Cancer Center supports the international committee of medical journal editors (ICMJE) and the ethical obligation of responsible sharing of data from clinical trials. The protocol summary, a statistical summary, and informed consent form will be made available on clinicaltrials.gov when required as a condition of Federal awards, other agreements supporting the research and/or as otherwise required. Requests for deidentified individual participant data can be made beginning 12 months after publication and for up to 36 months post publication. Deidentified individual participant data reported in the manuscript will be shared under the terms of a Data Use Agreement and may only be used for approved proposals. Requests may be made to: crdatashare@mskcc.org.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 31, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06954337
Lead sponsor
Memorial Sloan Kettering Cancer Center
Responsible party
Sponsor
First posted
May 1, 2025
Start date
May 1, 2025
Primary completion
Mar 1, 2027 (estimated)
Completion
May 1, 2027 (estimated)
Last update
Jul 31, 2026

Study contacts

Erin Bange, MD, MSCE
Contact
bangee@mskcc.org
646-422-4680
Deborah Schrag, MD, MPH
Contact
212-639-5851
Erin Bange, MD, MSCE
principal investigator · Memorial Sloan Kettering Cancer Center

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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