Lexington, KYNCT05548413Now EnrollingIRB Ready

Medication Adherence Clinical Trial in Lexington, KY

Access cutting-edge medication adherence treatment through this clinical trial at a research site in Lexington. Study-provided care at no cost to qualified participants.

Sponsored by Jia-Rong Wu

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Expert Care in Lexington

Access medication adherence specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related medication adherence treatment provided free

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Check if you qualify for this medication adherence clinical trial in Lexington, KY

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Lexington

    Convenient for KY residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Lexington site if eligible
  4. 4Begin participation

About This Medication Adherence Study in Lexington

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.

Sponsor: Jia-Rong Wu

Who Can Participate

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

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Lexington?

Yes, this clinical trial (NCT05548413) has an active research site in Lexington, KY that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Medication Adherence Treatment Options in Lexington, KY

If you're searching for medication adherence treatment options in Lexington, KY, this clinical trial (NCT05548413) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Lexington research site is actively enrolling participants for this clinical trial. You'll receive care from experienced medication adherence specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all medication adherence clinical trials near you to find additional studies recruiting in your area.

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