Using Text Messages to Improve Oral Chemotherapy for Adolescents and Adults With Acute Lymphoblastic Leukemia
Part of paid clinical trials in Chicago, Illinois.
- Sponsor
- University of Chicago
- Study ID
- NCT06446661
- Status
- Recruiting
Conditions
- Acute Lymphoblastic Leukemia
- T-cell Lymphoblastic Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 15 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- High Intensity — OTHERDaily texts
- No Text Messagings — OTHERStandard Care
- Low Intensity Text Messaging — OTHERWeekly Texts
Study Details
This is a single center 2-phase study to assess effects of using text messages on adherence to oral chemotherapy for patients with acute lymphoblastic leukemia (ALL) or T-cell lymphoblastic lymphoma.
Key Dates
- First listed
- Jun 6, 2024
- Start date
- May 19, 2026
- Status verified
- Jul 2026
- Primary completion
- Jun 15, 2027
- Completion
- Jun 15, 2028
Study Design
- Enrollment
- 48 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- OTHER
Arms
- Active Comparator: Efficacy Phase: High Intensity MessagingReceives high-intensity text messaging for 2 cycles of treatment
- Active Comparator: Efficacy Phase: Low Intensity MessagingReceives no texts for 1st cycle and low-intensity texts for 2nd cycle
- Experimental: Pilot Phase ArmParticipants receive high-intensity text messaging for 28 days
Primary Outcome Measure
To compare adherence to oral chemotherapy between study groups for first treatment cycle (Efficacy Phase) [ Time Frame: 84 days after completion of enrollment to efficacy phase of study ]
Central Contacts
- Clinical Trials Intake1-855-702-8222
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Chicago Medicine Comprehensive Cancer Center | Chicago | Illinois | 60637 | Austin Wesevich (PRINCIPAL_INVESTIGATOR) |
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