Improving Medication Adherence Using Family-focused and Literacy-sensitive Strategies
Jia-Rong Wu · with National Institute of Nursing Research (NINR) · NCT05548413
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 328
- US sites recruiting
- 1
- Study start
- January 4, 2023
- Record last updated
- May 5, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
People with heart failure who do not take their medications as prescribed are at high risk of complications leading to hospitalization, death and poor quality of life. In the proposed intervention, nurses will use easy-to-understand language to coach patients and their care partners to help them work together and build skills to overcome their individual barriers to adherence in order to 1) improve and sustain patient medication adherence; 2) reduce hospitalization; 3) improve quality of life. If effective, this intervention will support long-term medication adherence, thus reducing hospitalizations related to heart failure and quality of life.
Being studied: FamLit; Attention Control
Conditions: Medication Adherence; Heart Failure
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria - Patient Participants
- confirmed diagnosis of heart failure (HF), either systolic or diastolic HF
- ave suboptimal medication adherence
- have a care partner (CP) (either spouse, daughter/son, partner, other relative, friend) who is identified by the patient as the person most involved in HF care
- willingness to have a CP be involved in their medication taking
- have undergone evaluation of HF and prescribed stable doses of HF medications for at least 3 months
- live in a setting where the patient is responsible for their ow medication administration
- willing to use the SimpleMed+ (i.e., an electronic pillbox to measure objective medication adherence)
- availability by phone
Exclusion Criteria - Patient Participants
- cognitive impairment as indicated by having difficulties to understand and give informed consent
- a recent hospitalization within 3 months of study enrollment
- co-existing end-stage renal disease or terminal illness such as advanced malignancy, or any other condition with less than 1-year life expectancy
- psychotic illness
- current alcohol dependence or other substance abuse
- inability to speak English or other communication barrier
- currently or have received any similar self-care intervention recently in the past year
Inclusion Criteria - Care Partners
- unpaid family member, friend, partner, or other relation who is involved in the patients' care at least 3 times a week, designated by the patient
- willing to receive interventions with the patient together
- 18 years of age or older
Exclusion Criteria - Care Partners
- cognitive impairment as indicated by having difficulties to understand and give informed consent
- coexisting terminal illness
- non-English speaking or any other communication barrier
Recruiting US locations
Jia-Rong Wu
Lexington, KY 40536
Site contact: Jia-Rong Wu, PhD · 859-323-4712 · jiarong.wu2@uky.edu
Study contacts (from the official record)
- Jia-Rong Wu, PhD · 8593234712 · jiarong.wu2@uky.edu
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