RECRUITING

Pharmacy-led Transitions of Care Intervention to Improve Medication Adherence

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2024-04-06
Study Completion:2028-01-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06374277

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Medicaid or uninsured inpatients
  2. * 21 years or older
  3. * ≥2 of the complex chronic conditions during index admission or prescribed/using ≥2 chronic medications for these conditions
  4. * Patients receiving chronic disease medications from the hospital pharmacy.
  5. * 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.
  1. * Medicare and Medicaid dual eligible patients.
  2. * If the primary reason for the index admission is related to cancer, pregnancy, or a surgical procedure for an acute problem
  3. * If patients have diagnoses of active psychosis, substance abuse, or suicidal ideation during the index admission.
  4. * If the planned discharge location is not home.
  5. * If patients are part of an existing pharmacy discharge program.

Contacts and Locations

Study Contact

Satya Surbhi, PhD
CONTACT
646-438-0919
ssurbhi@uthsc.edu
Elizabeth A Tolley, PhD
CONTACT
901.422.6733
btolley@uthsc.edu

Principal Investigator

Satya Surbhi, PhD
PRINCIPAL_INVESTIGATOR
UTHSC

Study Locations (Sites)

University of Tennessee Medical Center
Knoxville, Tennessee, 37920
United States
University of Tennessee Health Science Center/Regional One Health
Memphis, Tennessee, 38103
United States

Collaborators and Investigators

Sponsor: University of Tennessee

  • Satya Surbhi, PhD, PRINCIPAL_INVESTIGATOR, UTHSC

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-04-06
Study Completion Date2028-01-31

Study Record Updates

Study Start Date2024-04-06
Study Completion Date2028-01-31

Terms related to this study

Additional Relevant MeSH Terms

  • Diabetes
  • Hypertension
  • High Cholesterol/Hyperlipidemia
  • Coronary Artery Disease
  • Congestive Heart Failure
  • Chronic Lung Disease
  • Chronic Kidney Diseases
  • Arrythmia
  • Stroke
  • Depression
  • Anxiety
  • Pulmonary Embolism
  • Heart Attack