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Breast CancerNCT06954337

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

A study testing Usual practice pattern (UPP) and Experimental: Enhanced Telehealth (ET) in people with Breast Cancer and Prostate Cancer, run by Memorial Sloan Kettering Cancer Center at 7 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial 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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Breast Cancer, Prostate Cancer
What is being tested?
Usual practice pattern (UPP) and Experimental: Enhanced Telehealth (ET)
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1,750 participants
Where
7 sitesUnited States
Study dates
1 May 2025to 1 May 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

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

Who cannot join

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

Trial locations and contacts

7 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Erin Bange, MD, MSCE contact

646-422-4680

bangee@mskcc.org

Deborah Schrag, MD, MPH contact

212-639-5851

7 sites in 1 country

United States7 sites, 7 recruiting
  • Memorial Sloan Kettering Basking Ridge (All Protocol Activities)

    Basking Ridge, New Jersey, 07920

    Erin Bange, MD, MSCE, 646-422-4680

    Recruiting
  • Memorial Sloan Kettering Suffolk - Commack (All Protocol Activities)

    Commack, New York, 11725

    Erin Bange, MD, MSCE, 646-422-4680

    Recruiting
  • Memorial Sloan Kettering Westchester (All Protocol Activities)

    Harrison, New York, 10604

    Erin Bange, MD, MSCE, 646-422-4680

    Recruiting
  • Memorial Sloan Kettering Monmouth (All Protocol Activities)

    Middletown, New Jersey, 07748

    Erin Bange, MD, MSCE, 646-422-4680

    Recruiting
  • Memorial Sloan Kettering Bergen (All Protocol Activities)

    Montvale, New Jersey, 07645

    Erin Bange, MD, MSCE, 646-422-4680

    Recruiting
  • Memorial Sloan Kettering Cancer Center (All Protocol Activites)

    New York, New York, 10065

    Erin Bange, MD, MSCE, 646-422-4680

    Recruiting
  • Memorial Sloan Kettering Nassau (All Protocol Activities)

    Uniondale, New York, 11553

    Erin Bange, MD, MSCE, 646-422-4680

    Recruiting

Other trials in United States

About this study

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.

Being tested
Usual practice pattern (UPP), Experimental: Enhanced Telehealth (ET)
Keywords
Telehealth, Cancer Care at Home, 25-055
Medical subject headings
Breast Neoplasms, Prostatic Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Usual practice pattern (UPP)Other

    Patient follows usual practice pattern for routine care

  • Experimental: Enhanced Telehealth (ET)Other

    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

Study groups in NCT06954337
Study groupRoleWhat they receive
Usual practice pattern (UPP)Active comparatorUsual practice pattern (UPP) of patient's medical oncologist
Receives: Other: Usual practice pattern (UPP); Other: Experimental: Enhanced Telehealth (ET)
Enhanced Telehealth (ET)ExperimentalEnhanced Telehealth (ET) practice pattern of patient's medical oncologist
Receives: Other: Usual practice pattern (UPP); Other: Experimental: Enhanced Telehealth (ET)

What is being measured

The primary outcome is the main question the study is designed to answer.

  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

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 May 2025
  2. Study start1 May 2025
  3. Primary completion1 Mar 2027 (estimated)
  4. Study completion1 May 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
1,750 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06954337
Sponsor's protocol ID
25-055
Status last verified
Oct 2026
First submitted
24 Apr 2025
Last updated
3 Nov 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
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.

Questions about this trial

What is this clinical trial studying?

A study testing Usual practice pattern (UPP) and Experimental: Enhanced Telehealth (ET) in people with Breast Cancer and Prostate Cancer, run by Memorial Sloan Kettering Cancer Center at 7 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 3 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 7 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Erin Bange, MD, MSCE (646-422-4680, bangee@mskcc.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Proportion of routine face to face medical oncology related visits out of total medical oncology related visits (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Nov 2026.

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