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Recruiting NCT07073807

NCT07073807 Mobile Health Intervention to Improve Adherence to Oral Anticancer Therapy

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Clinical Trial Summary
NCT ID NCT07073807
Status Recruiting
Phase
Sponsor University of California, Irvine
Condition Cancer
Study Type INTERVENTIONAL
Enrollment 35 participants
Start Date 2025-08-26
Primary Completion 2026-08

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
All Conditions
Interventions
SMART Intervention using TAPPT® for Adherence, Symptom, Financial, and Social Needs Monitoring

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 35 participants in total. It began in 2025-08-26 with a primary completion date of 2026-08.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

New oral anticancer treatments have improved survival across cancer types but introduced challenges in medication adherence and symptom management. The SMART pilot trial will test a new mobile health intervention that facilitates remote adherence and symptom monitoring, patient-provider communication outside of clinic visits regarding the use of oral anticancer treatments, and support for financial and social needs, as well as health literacy support, for 30 English- and Spanish-speaking patients. This study will increase understanding of barriers and facilitators to the use of the proposed mHealth intervention.

Eligibility Criteria

Inclusion Criteria: * Must speak English or Spanish * Must be 18 years of age or older * Have a diagnosis of any type and stage of cancer * Have a new prescription for an oral anticancer therapy (OAT) initiated within the last 90 days or planned to start within the next 15 days * Be receiving treatment at UCI Chao Family Comprehensive Cancer Center-affiliated oncology clinics * Own a smartphone and be willing to receive study-related text messages. Exclusion Criteria: * Have an Eastern Cooperative Oncology Group (ECOG) performance status greater than 2 * Be medically or cognitively unable to give consent or participate in the study * Be participating in another clinical trial that monitors adherence or symptoms related to the newly prescribed OAT

Contact & Investigator

Central Contact

Gelareh Sadigh, MD

✉ gsadigh@hs.uci.edu

📞 (714) 456-3610

Frequently Asked Questions

Who can join the NCT07073807 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07073807 currently recruiting?

Yes, NCT07073807 is actively recruiting participants. Contact the research team at gsadigh@hs.uci.edu for enrollment information.

Where is the NCT07073807 trial being conducted?

This trial is being conducted at Irvine, United States, Newport Beach, United States, Newport Beach, United States, Orange, United States and 1 additional location.

Who is sponsoring the NCT07073807 clinical trial?

NCT07073807 is sponsored by University of California, Irvine. The trial plans to enroll 35 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology