Smartphone app and wearable sensor team up to catch infections early in cancer care

NCT ID NCT07810400

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Sep 09, 2026 · Last updated Sep 11, 2026 · Updated 2 times

Summary

Researchers at Mayo Clinic are studying a remote monitoring program called SHIELD for cancer patients who are starting systemic therapy. Participants use a smartphone app to report symptoms and wear a small temperature sensor. The app and sensor send data to the medical record, where nurses and clinical assistants can review alerts and decide if a patient needs care. The study checks whether this approach is practical, acceptable, and able to catch infectious complications early.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
A remote monitoring program combining a smartphone app for symptom reporting with a wearable continuous temperature sensor
What this could lead to
If it works, cancer patients starting treatment could spot infections earlier from home, possibly avoiding emergency visits and catching problems before they become serious.
What could go wrong
This is an early implementation study, not a test of whether the program saves lives. Patients may not stick with the app or sensor, alerts may overwhelm clinic staff, and the program may not work outside Mayo Clinic.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 470 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Nov 2026

An estimate. Start dates often move.

Expected to finish

Jun 2031

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

1 year and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Patient Inclusion Criteria, Aim 1: * Documented history of cancer * Actively receiving cancer care at any Mayo Clinic Midwest practice site * Involved in or impacted by the care or participation of eligible patients Patient Inclusion Criteria, Aim 2 * Documented diagnosis of cancer * ≥ 1 year of age as the CTM device only supports these ages * Initiating systemic cancer-directed treatment at a Mayo Clinic Midwest site * Able to read and speak English or Spanish (or have a caregiver capable of either) as the current technologies only support those languages Caregiver Inclusion Criteria * Age 18 years or older. * Identified as the eligible minor pediatric patient's parent or legal guardian Healthcare Professional Inclusion Criteria * A hematology/oncology clinical, research, RPM, operational, administrative, managerial, or technical/electronic health record (EHR) or other healthcare professional supporting or supervising, or directly affected by the SHIELD program development and pilot implementation study at a participating Mayo Clinic Health System site or Mayo Clinic in Rochester work unit. Exclusion Criteria: Patient Exclusion Criteria: * History of hematopoietic cell transplant or adoptive cellular or bispecific antibody therapy \[i.e., chimeric antigen receptor (CAR) T-cell (CAR-T)\] within the prior 100 days * Enrolled in hospice or expected life span \< 6 months Caregiver and Healthcare Professional Exclusion Criteria * Unable or unwilling to provide consent to participate in study procedures

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

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  1. The study's own enquiry address

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  2. The places running it

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  3. The official record

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  4. A doctor treating you

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Contacts and locations

Study contacts

  • Contact

    Email: •••••@•••••

Locations

  • Mayo Clinic in Rochester

    Rochester, Minnesota, 55905, United States

    Contact Email: •••••@•••••

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