RecruitingNot ApplicableNCT06374277

Pharmacy-led Transitions of Care Intervention to Improve Medication Adherence

Pharmacy-led Transitions of Care Intervention to Address System-Level Barriers and Improve Medication Adherence in Socioeconomically Disadvantaged Populations


Sponsor

University of Tennessee

Enrollment

388 participants

Start Date

Apr 6, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Socioeconomically disadvantaged populations with multiple chronic conditions have high rates of nonadherence to essential chronic disease medications after hospital discharge. Medication nonadherence after hospital discharge is significantly associated with increased mortality and higher rates of readmissions and costs among these patients. Major patient-reported barriers to essential medication use after hospital discharge among low-income individuals are related to social determinants of health (SDOH) and include: 1) financial barriers , 2) transportation barriers, and 3) system-level barriers. Although, medication therapy management services are important during care transitions, these services have not proven effective in improving medication adherence after hospital discharge, highlighting a critical need for innovative interventions. The Medication Affordability, Accessibility, and Availability in Care Transitions (Med AAAction) Study will test the effectiveness of a pharmacy-led care transitions intervention versus usual care through a pragmatic randomized controlled trial of 388 Medicaid and uninsured hospital in-patients with MCC from three large healthcare systems in Tennessee. The intervention will involve: 1) medications with zero copay, 2) bedside delivery then home delivery of medications, and 3) care coordination provided by certified pharmacy technicians/health coaches to assist with medication access, medication reconciliation, and rapid and ongoing primary care follow-up. We will examine the impact of the intervention during 12 months on 1) medication adherence (primary outcome) and 2) rapid primary care follow-up, 30-day readmissions, hospitalizations and emergency department visits, and costs. We will conduct key informant interviews to understand patient experience with the acre received during and after care transitions. By examining effectiveness of the intervention on outcomes including medication adherence, health care utilization, costs, and patient experience, this study will provide valuable results to health systems, payers, and policymakers to assist in future implementation and sustainability of the intervention for socioeconomically disadvantaged populations.


Eligibility

Min Age: 18 Years

Inclusion Criteria5

  • Medicaid or uninsured inpatients
  • years or older
  • ≥2 of the complex chronic conditions during index admission or prescribed/using ≥2 chronic medications for these conditions
  • Patients receiving chronic disease medications from the hospital pharmacy.
  • Patients will be eligible if they have multiple complex chronic conditions including diabetes, hypertension, high cholesterol, coronary artery disease, congestive heart failure, chronic lung disease, chronic kidney disease, arrhythmia, stroke, psychiatric disorders including depression and anxiety, or who are prescribed or using anticoagulants.

Exclusion Criteria5

  • Medicare and Medicaid dual eligible patients.
  • If the primary reason for the index admission is related to cancer, pregnancy, or a surgical procedure for an acute problem
  • If patients have diagnoses of active psychosis, substance abuse, or suicidal ideation during the index admission.
  • If the planned discharge location is not home.
  • If patients are part of an existing pharmacy discharge program.

Interventions

OTHERMed AAAction intervention

The Med AAAction intervention will include the following components: 1) medications with zero copay, 2) bedside delivery and subsequent home delivery of medications, and 3) care coordination provided by certified pharmacy technicians/health coaches to assist with medication access, medication reconciliation, and rapid and ongoing primary care follow-up after hospital discharge. The intervention will be provided for one-year.


Locations(2)

University of Tennessee Medical Center

Knoxville, Tennessee, United States

University of Tennessee Health Science Center/Regional One Health

Memphis, Tennessee, United States

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NCT06374277


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