Oral Adherence in Hematological Oncology Agents and Impact on Comorbid Therapy Adherence

NARecruitingINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

February 8, 2021

Primary Completion Date

December 31, 2023

Study Completion Date

December 31, 2023

Conditions
Chronic Myeloid LeukemiaChronic Lymphocytic LeukemiaMultiple MyelomaMultiple Chronic Conditions
Interventions
OTHER

Patient-reported outcome measure

Participants will complete a patient-reported outcome measure for their oral anticancer agent at two timepoints over 2 months, to assess patient symptoms and adherence to their oral anticancer agent.

OTHER

Comprehensive Medication Review

Following the first patient-reported outcome measure, participants will be contacted by the community pharmacist for a Comprehensive Medication Review (CMR) for their chronic medications. A follow-up CMR will take place after the second patient-reported outcome measure.

OTHER

Pharmacist communication

Throughout the study, the oncology and community pharmacists will communicate about medications through the electronic medical record.

Trial Locations (1)

37232

RECRUITING

Vanderbilt University Medical Center, Nashville

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Vanderbilt University Medical Center

OTHER

collaborator

AstraZeneca

INDUSTRY

lead

University of Tennessee

OTHER