Clinical trial Recruiting at 1 site Observational Ages 18 and up

SMS text check-ins to track symptoms for people with plasma cell disorders

Official title: SMS-Based Remote Symptom Monitoring for Patients With Plasma Cell Disorders

Run by Mayo Clinic · NCT07850284 · Data updated 2026-11-12

This study tests whether daily SMS symptom prompts are feasible and acceptable for adults starting treatment for multiple myeloma or AL amyloidosis.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment150 (estimated)
SponsorMayo Clinic
Academic / other
Locations1 site (Rochester, Minnesota)
StatusRecruiting
StartedAugust 25, 2026
Main results expectedAugust 25, 2028
Study endsAugust 25, 2028
Registry record updatedSeptember 30, 2026
Trial IDNCT07850284 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) starting a new treatment for MM or AL amyloidosis within about two weeks of enrollment and able to provide informed consent.

Probably not a fit

Patients who are unable to provide informed consent or who do not have access to or preferences against SMS communication may not benefit.

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

What this trial studies

This observational, non-interventional study from Mayo Clinic explores using everyday text message reminders to monitor symptoms in adults starting a new therapy for MM or AL amyloidosis. Researchers aim to see if this approach is feasible, acceptable, and capable of identifying symptoms early that may need clinical attention. The study does not assign a treatment but observes how patients respond to routine SMS monitoring during their care.

Why it matters

Potential benefit: If successful, daily text-based monitoring could help patients and clinicians catch troubling symptoms earlier, potentially improving safety and communication.

How similar studies have gone: Prior work in other cancers and chronic conditions suggests SMS-based monitoring is feasible and acceptable, with potential for early symptom detection, though results vary by context.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age \>= 18 years
* Diagnosis of MM or AL based on IMWG diagnostic criteria
* Planned to start a new treatment within 14 days (+/-7 days)
* Able to provide written informed consent

Exclusion Criteria:

* Not able to give informed consent

Where it's running

  • Mayo Clinic in Rochester
    Rochester, Minnesota, 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.