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Recruiting NCT07553572

NCT07553572 Remote Monitoring and Symptom Management Digital Application

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Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07553572
Status Recruiting
Phase
Sponsor Patrick C. Johnson, MD
Condition Breast Cancer (Locally Advanced or Metastatic)
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2026-04-14
Primary Completion 2026-11-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
ASSIST phone application

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 60 participants in total. It began in 2026-04-14 with a primary completion date of 2026-11-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this clinical trial is to learn if an artificial intelligence phone application called ASSIST can help patients receiving cancer treatment. The main question\[s\] it aims to answer are: Is ASSIST feasible for patients (meaning can it be used by patients)? Is ASSIST acceptable to patients (meaning do patients like it)? Researchers will compare the ASSIST phone application to see how it compares to usual clinical care. Participants on the ASSIST arm will use the ASSIST phone application for 12 weeks, and participants in both groups will complete surveys.

Eligibility Criteria

Inclusion Criteria: 1. Age 18 years or older 2. Ability to understand English 3. About to begin definitive systemic treatment (or within 4 weeks of beginning treatment) based upon the oncology treatment intent form for a new diagnosis of breast cancer, colorectal cancer, or lymphoma. 4. Expected treatment duration of at least 12 weeks 5. Own or willing to receive a smartphone Exclusion Criteria: 1. Cognitive impairment that would interfere with ability to use smartphone application (as assessed by their attending physician) 2. Visual or motor impairment that would prevent smartphone use 3. Expected survival less than 3 months

Contact & Investigator

Central Contact

Patrick C Johnson, MD

✉ pcjohnson@mgh.harvard.edu

📞 6177244000

Frequently Asked Questions

Who can join the NCT07553572 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Breast Cancer (Locally Advanced or Metastatic). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07553572 currently recruiting?

Yes, NCT07553572 is actively recruiting participants. Contact the research team at pcjohnson@mgh.harvard.edu for enrollment information.

Where is the NCT07553572 trial being conducted?

This trial is being conducted at Boston, United States.

Who is sponsoring the NCT07553572 clinical trial?

NCT07553572 is sponsored by Patrick C. Johnson, MD. The trial plans to enroll 60 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology