Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Phone app for remote symptom monitoring and management during cancer treatment

Official title: Pilot Randomized Controlled Trial of a Remote Monitoring and Symptom Management Intervention (ASSIST) Among Patients Receiving Systemic Therapy

Run by Massachusetts General Hospital · NCT07553572 · Data updated 2026-11-12

This trial will test whether the ASSIST smartphone app can be used and is liked by people with breast cancer, colorectal cancer, or lymphoma who are starting systemic treatment.

More Colorectal Cancer trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorMassachusetts General Hospital
Academic / other
Locations1 site (Boston, Massachusetts)
StatusRecruiting
StartedApril 14, 2026
Main results expectedNovember 30, 2026
Study endsMarch 31, 2027
Registry record updatedApril 28, 2026
Trial IDNCT07553572 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) with locally advanced or metastatic breast cancer, colorectal cancer, or lymphoma who are starting systemic treatment within about four weeks, expect treatment for at least 12 weeks, can read English, and have or can receive a smartphone are ideal candidates.

Probably not a fit

Patients with cognitive, visual, or motor impairments that prevent smartphone use, those who cannot use English, or those with expected survival under three months are unlikely to benefit from this app-based intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Participants will be assigned to use the ASSIST phone application for 12 weeks or to receive usual clinical care, and participants in both groups will complete regular surveys. The app uses artificial intelligence to collect patient-reported symptoms and deliver remote monitoring and symptom-management support. The study focuses on feasibility (can patients use the app) and acceptability (do patients like it) rather than clinical outcomes. Enrollment is limited to adults starting definitive systemic therapy who can read English and have or will receive a smartphone.

Why it matters

Potential benefit: If successful, ASSIST could help detect and manage treatment symptoms earlier and improve the patient experience during systemic cancer therapy.

How similar studies have gone: Prior research on remote symptom monitoring and patient-reported outcome apps in oncology has shown improved symptom control and quality-of-life measures, so the approach has supporting evidence though ASSIST itself is being specifically tested for feasibility and acceptability.

Who can join: the full rules

Show full inclusion / exclusion 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

Where it's running

  • Massachusetts General Hospital
    Boston, Massachusetts, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.