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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05183763
Other study ID # 2020-2221
Secondary ID R01HL153750
Status Recruiting
Phase N/A
First received
Last updated
Start date March 7, 2022
Est. completion date April 30, 2027

Study information

Verified date April 2024
Source Tulane University
Contact Erin M Peacock, PhD, MPH
Phone 504-988-1075
Email epeacoc@tulane.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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) >=50 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 402
Est. completion date April 30, 2027
Est. primary completion date April 30, 2026
Accepts healthy volunteers No
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria: - 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 next year - English-speaking - telephone access - aged =50 years - diagnosis of essential hypertension (ICD-10-CM code I10) - currently filling antihypertensive medication - low antihypertensive medication refill (proportion of days covered (PDC) <0.8) - low self-report adherence (4-item Krousel-Wood Medication Adherence Scale (K-Wood-MAS-4) score =1) - uncontrolled blood pressure (BP) (systolic BP =130 mm Hg or diastolic BP =80 mm Hg) - desire to improve BP Exclusion Criteria: - living in a household with someone already enrolled in the study - enrollment in another clinical trial for drug adherence or BP control - moderate to severe cognitive impairment

Study Design


Intervention

Behavioral:
STAR-MAP health coaching
Interactive health coaching delivered in 11 sessions over one year; focusing on using adaptive change tactics to improve medication-taking behavior
Medication reminder tools
Medication-taking reminder app and pillbox

Locations

Country Name City State
United States Pennington Biomedical Research Center Baton Rouge Louisiana
United States Tulane Doctors Dermatology & Multispecialty Clinic Covington Louisiana
United States Tulane Doctors Heart & Vascular and Primary Care Clinic Metairie Louisiana
United States Tulane University Clinical and Translational Unit New Orleans Louisiana
United States LSU Health Sciences Shreveport Clinical Trials Office Shreveport Louisiana

Sponsors (4)

Lead Sponsor Collaborator
Tulane University Minds at Work, National Heart, Lung, and Blood Institute (NHLBI), Ohio State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Difference in mean change in 4-item Krousel-Wood Medication Adherence Scale score, baseline to 6 months Self-reported adherence measured by 4-item Krousel-Wood Medication Adherence Scale (K-Wood-MAS-4; minimum value: 0 (better adherence); maximum value: 4 (worse adherence)) Baseline to 6 months
Other Difference in proportion with 4-item Krousel-Wood Medication Adherence Scale score <1 at 6 months Self-reported adherence measured by 4-item Krousel-Wood Medication Adherence Scale (K-Wood-MAS-4; minimum value: 0 (better adherence); maximum value: 4 (worse adherence)) 6 months
Other Difference in change in proportion with high adherence as measured by urine metabolite analysis, baseline to 6 months Adherence determined by liquid chromatography tandem mass spectrometry analysis of urinary metabolites of antihypertensive medications Baseline to 6 months
Other Difference in proportion with controlled BP at 6 months Controlled blood pressure (BP) defined as systolic BP <130 mm Hg and diastolic BP <80 mm Hg; BP measured using standardized protocol 6 months
Other Difference in mean change in SBP, baseline to 6 months Systolic blood pressure (SBP) measured using standardized protocol Baseline to 6 months
Other Difference in mean change in DBP, baseline to 6 months Diastolic blood pressure (DBP) measured using standardized protocol Baseline to 6 months
Other Difference in mean change in health-related quality of life scores, baseline to 6 months Quality of life measured using 12-item Short Form Survey (SF-12); scores for eight subscales, Mental Component Summary, and Physical Component Summary calculated and compared (minimum: 0 (worse quality of life); maximum: 100 (better quality of life)) Baseline to 6 months
Other Difference in proportion with PDC >=0.8 at 24 months Proportion of days covered (PDC) calculated from pharmacy refill data 24 months
Other Difference in mean change in PDC, baseline to 24 months Proportion of days covered (PDC) calculated from pharmacy refill data Baseline to 24 months
Other Difference in mean change in 4-item Krousel-Wood Medication Adherence Scale score, baseline to 24 months Self-reported adherence measured by 4-item Krousel-Wood Medication Adherence Scale (K-Wood-MAS-4; minimum value: 0 (better adherence); maximum value: 4 (worse adherence)) Baseline to 24 months
Other Difference in proportion with 4-item Krousel-Wood Medication Adherence Scale score <1 at 24 months Self-reported adherence measured by 4-item Krousel-Wood Medication Adherence Scale (K-Wood-MAS-4; minimum value: 0 (better adherence); maximum value: 4 (worse adherence)) 24 months
Other Difference in change in proportion with high adherence as measured by urine metabolite analysis, baseline to 24 months Adherence determined by liquid chromatography tandem mass spectrometry analysis of urinary metabolites of antihypertensive medications Baseline to 24 months
Other Difference in proportion with controlled BP at 24 months Controlled blood pressure (BP) defined as systolic BP <130 mm Hg and diastolic BP <80 mm Hg; BP measured using standardized protocol 24 months
Other Difference in mean change in SBP, baseline to 24 months Systolic blood pressure (SBP) measured using standardized protocol Baseline to 24 months
Other Difference in mean change in DBP, baseline to 24 months Diastolic blood pressure (DBP) measured using standardized protocol Baseline to 24 months
Other Difference in mean change in health-related quality of life scores, baseline to 24 months Quality of life measured using 12-item Short Form Survey (SF-12); scores for eight subscales, Mental Component Summary, and Physical Component Summary calculated and compared (minimum: 0 (worse quality of life); maximum: 100 (better quality of life)) Baseline to 24 months
Primary Difference in proportion with PDC >=0.8 at 12 months Proportion of days covered (PDC) calculated from pharmacy refill data 12 months
Secondary Difference in mean change in PDC, baseline to 12 months Proportion of days covered (PDC) calculated from pharmacy refill data Baseline to 12 months
Secondary Difference in mean change in 4-item Krousel-Wood Medication Adherence Scale score, baseline to 12 months Self-reported adherence measured by 4-item Krousel-Wood Medication Adherence Scale (K-Wood-MAS-4; minimum value: 0 (better adherence); maximum value: 4 (worse adherence)) Baseline to 12 months
Secondary Difference in proportion with 4-item Krousel-Wood Medication Adherence Scale score <1 at 12 months Self-reported adherence measured by 4-item Krousel-Wood Medication Adherence Scale (K-Wood-MAS-4; minimum value: 0 (better adherence); maximum value: 4 (worse adherence)) 12 months
Secondary Difference in change in proportion with high adherence as measured by urine metabolite analysis, baseline to 12 months Adherence determined by liquid chromatography tandem mass spectrometry analysis of urinary metabolites of antihypertensive medications Baseline to 12 months
Secondary Difference in proportion with controlled BP at 12 months Controlled blood pressure (BP) defined as systolic BP <130 mm Hg and diastolic BP <80 mm Hg; BP measured using standardized protocol 12 months
Secondary Difference in mean change in SBP, baseline to 12 months Systolic blood pressure (SBP) measured using standardized protocol Baseline to 12 months
Secondary Difference in mean change in DBP, baseline to 12 months Diastolic blood pressure (DBP) measured using standardized protocol Baseline to 12 months
Secondary Difference in mean change in health-related quality of life scores, baseline to 12 months Quality of life measured using 12-item Short Form Survey (SF-12); scores for eight subscales, Mental Component Summary, and Physical Component Summary calculated and compared (minimum: 0 (worse quality of life); maximum: 100 (better quality of life)) Baseline to 12 months
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