Text messages to help sticking with oral chemotherapy in ALL and T-cell lymphoma
Official title: Improving Oral Chemotherapy Adherence in Maintenance for Adolescents and Adults With Acute Lymphoblastic Leukemia and T-cell Lymphoblastic Lymphoma Using Text Messages
Run by University of Chicago · NCT06446661 · Data updated 2026-11-12
Researchers are testing whether sending high‑frequency text reminders helps teens and adults on oral mercaptopurine and methotrexate stick with their treatment.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 15 Years and up |
| Sex | All |
| Enrollment | 48 (estimated) |
| Sponsor | University of Chicago Academic / other |
| Drugs / interventions | methotrexate, chemotherapy |
| Locations | 1 site (Chicago, Illinois) |
| Status | Recruiting |
| Started | May 19, 2026 |
| Main results expected | June 15, 2027 |
| Study ends | June 15, 2028 |
| Registry record updated | July 10, 2026 |
| Trial ID | NCT06446661 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Patients aged 15 and older with ALL or T‑cell lymphoblastic lymphoma receiving maintenance therapy including mercaptopurine and methotrexate.
✕Probably not a fit
Patients without access to a cell phone or who do not wish to participate 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 single‑center study has two phases. In a 28‑day pilot, participants rate how acceptable the text message reminders are. In the efficacy phase, adherence to oral chemotherapy will be compared between high‑intensity text messaging and standard care, with the goal of improving adherence during the first treatment cycle.
Why it matters
Potential benefit: If successful, patients may have better adherence to oral chemotherapy, which could improve treatment effectiveness.
How similar studies have gone: Previous work in other cancers and settings suggests text reminders can improve medication adherence, but results vary by context.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age of 15 years or older at time of enrollment * Diagnosed with ALL or T-cell lymphoblastic lymphoma * Currently receiving treatment with pediatric-based regimen that includes maintenance with mercaptopurine and methotrexate (e.g., CALGB 10403). Study participation begins with the start of maintenance, so enrollment occurs prior to the start of maintenance. Patients in the pilot phase may have already started maintenance as long as the end of their maintenance therapy is scheduled to occur after the end of the 28-day pilot intervention. Exclusion Criteria: * Patient or caregiver who would receive text message reminders does not have a cell phone that receives text messages * Patient does not wish to participate * Text messages will be crafted in the patient's preferred language for medical communication, so English fluency is not an enrollment requirement.
Where it's running
-
University of Chicago Medicine Comprehensive Cancer Center
Chicago, Illinois, United States Recruiting
Study contacts
- Principal investigator: Austin Wesevich — University of Chicago
- Study coordinator: Clinical Trials Intake
- Email: cancerclinicaltrials@bsd.uchicago.edu
- Phone: 1-855-702-8222
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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.