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Implementation of an Oral Chemotherapy Adherence Intervention
Sponsor: UNC Lineberger Comprehensive Cancer Center
Summary
The goal of this study is to evaluate the effectiveness and usability of a newly developed oral anticancer agent adherence program implemented across 6 cancer clinics (two academic, two urban, and two rural). The study will include 160 adult participants with either solid tumors or hematologic malignancies who have been taking oral anticancer agents for at least six months. This study will have two groups of participants, a pre- and post-implementation group. In the pre-implementation of the program group, investigators will administer a survey to the 80 participants and gather information about their medication prior to their enrollment of the program. Similarly, 80 participants who have been enrolled into this program for at least 6 months will serve as the post-implementation group. These patients will be administered the same survey. The results from both groups will be analyzed to see how effective the medication adherence program is.
Official title: Design and Implementation of a Social Cognitive Theory-based Medication Adherence Intervention
Key Details
Gender
All
Age Range
21 Years - Any
Study Type
INTERVENTIONAL
Enrollment
160
Start Date
2025-05-28
Completion Date
2028-08-30
Last Updated
2025-07-08
Healthy Volunteers
No
Conditions
Interventions
Multilevel Adherence Intervention
Participants enrolled in this adherence program will have individualized counseling sessions with their clinical pharmacists regarding their oral anticancer agent based on their risk-stratified monitoring category. Participants will be followed longitudinally and will receive tailored support.
Locations (1)
UNC Chapel Hill
Chapel Hill, North Carolina, United States