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Recruiting Not applicable Interventional

Medication Adherence Program

ClinicalTrials.gov ID: NCT05183763

Public ClinicalTrials.gov record NCT05183763. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 3:04 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Supporting Tailored Adaptive Change and Reinforcement for Medication Adherence Program: Randomized Trial of a Novel Approach to Improve Adherence in Older Hypertensive Women and Men

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Randomized controlled trial testing the efficacy of the Supporting Tailored Adaptive change and Reinforcement for Medication Adherence Program (STAR-MAP), a health coaching approach that aims to improve antihypertensive medication adherence, blood pressure control, and quality of life. Participants (n=402) \>=40 years old with a diagnosis of hypertension, uncontrolled blood pressure, and low antihypertensive medication adherence will be recruited through a statewide health insurer, Blue Cross Blue Shield of Louisiana, and randomized to receive either interactive health coaching sessions with medication reminder tools (intervention) or medication reminder tools only (control) over one year. Data will be collected from participants at baseline, 6 months, 12 months, and 24 months using questionnaires, physical measurement (height, weight, blood pressure), a computer-based single-category implicit association test, and laboratory analysis of antihypertensive medication urinary metabolites.

Study identification

NCT ID
NCT05183763
Recruitment status
Recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Tulane University
Other
Enrollment
402 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 6, 2022
Primary completion
Apr 29, 2027
Completion
Apr 29, 2027
Last update posted
Jun 11, 2026

2022 – 2027

United States locations

U.S. sites
5
U.S. states
1
U.S. cities
5
Facility City State ZIP Site status
Pennington Biomedical Research Center Baton Rouge Louisiana 70808 Recruiting
Tulane Doctors Dermatology & Multispecialty Clinic Covington Louisiana 70433 Recruiting
Tulane Doctors Heart & Vascular and Primary Care Clinic Metairie Louisiana 70002 Recruiting
Tulane University Clinical and Translational Unit New Orleans Louisiana 70112 Recruiting
LSU Health Sciences Shreveport Clinical Trials Office Shreveport Louisiana 71101 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05183763, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 11, 2026 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05183763 live on ClinicalTrials.gov.

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