Actively Recruiting

Phase Not Applicable
Age: 40Years +
All Genders
ID05183763

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

Led by Tulane University · Updated on 2026-05-20

402

Participants Needed

5

Research Sites

N/A

Total Duration

On this page

Sponsors

T

Tulane University

Lead Sponsor

O

Ohio State University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the Supporting Tailored Adaptive change and Reinforcement for Medication Adherence Program (STAR-MAP), a health coaching approach designed to improve medication adherence, blood pressure control, and quality of life for adults aged 40 and older with hypertension. This randomized controlled trial compares the STAR-MAP program with medication reminder tools alone among participants who have uncontrolled blood pressure and low adherence to antihypertensive medication. Participants are randomly assigned to one of two groups: one receives interactive health coaching sessions alongside medication reminder tools, while the other receives only the medication reminder tools. The coaching involves 11 sessions over one year, focusing on adaptive strategies to encourage better medication-taking behaviors. The study collects data at baseline, 6 months, 12 months, and 24 months. Throughout the study, participants undergo questionnaires, physical measurements including height, weight, and blood pressure, a computerized test of implicit associations, and laboratory analysis of urine for medication metabolites. Researchers aim to measure medication adherence using various scales and lab tests, blood pressure control, and health-related quality of life. The main outcome is the difference in medication adherence proportion at 12 months. Safety and progress are monitored over the two-year follow-up period.

CONDITIONS

Brief Title

Medication Adherence Program

Who Can Participate

Age: 40Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Fully insured by Blue Cross Blue Shield of Louisiana (BCBSLA)
  • Continuously enrolled in BCBSLA for one year
  • Planning to remain a member of BCBSLA for the next year
  • English-speaking
  • Telephone access
  • Aged 40 years or older
  • Diagnosis of essential hypertension (ICD-10-CM code I10)
  • Currently filling antihypertensive medication prescriptions
  • Low antihypertensive medication refill (proportion of days covered less than 0.8)
  • Low self-reported adherence (Krousel-Wood Medication Adherence Scale score 1 or higher)
  • Uncontrolled blood pressure (systolic BP 130 mm Hg or higher or diastolic BP 80 mm Hg or higher)
  • Desire to improve blood pressure
Not Eligible

You will not qualify if you...

  • Living in a household with someone already enrolled in the study
  • Enrollment in another clinical trial for drug adherence or blood pressure control
  • Moderate to severe cognitive impairment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or via telephone)

Outpatient Treatment

Duration - 11 sessions over one year

Participants receive either interactive health coaching combined with medication reminder tools or medication reminder tools only to improve medication adherence.

11 coaching sessions over one year

Trial Site Locations

Total: 5 locations

1

Pennington Biomedical Research Center

Baton Rouge, Louisiana, United States, 70808

Actively Recruiting

2

Tulane Doctors Dermatology & Multispecialty Clinic

Covington, Louisiana, United States, 70433

Actively Recruiting

3

Tulane Doctors Heart & Vascular and Primary Care Clinic

Metairie, Louisiana, United States, 70002

Actively Recruiting

4

Tulane University Clinical and Translational Unit

New Orleans, Louisiana, United States, 70112

Actively Recruiting

5

LSU Health Sciences Shreveport Clinical Trials Office

Shreveport, Louisiana, United States, 71101

Actively Recruiting

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Research Team

E

Erin M Peacock, PhD, MPH

M

Marie A Krousel-Wood, MD, MSPH

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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