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 type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 150 (estimated) |
| Sponsor | Mayo Clinic Academic / other |
| Locations | 1 site (Rochester, Minnesota) |
| Status | Recruiting |
| Started | August 25, 2026 |
| Main results expected | August 25, 2028 |
| Study ends | August 25, 2028 |
| Registry record updated | September 30, 2026 |
| Trial ID | NCT07850284 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
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Mayo Clinic in Rochester
Rochester, Minnesota, United States Recruiting
Study contacts
- Principal investigator: Nadine H. Abdallah, MD — Mayo Clinic in Rochester
- Study coordinator: Clinical Trials Referral Office
- Email: mayocliniccancerstudies@mayo.edu
- Phone: 855-776-0015
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.