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Trial · NCT03748420

Medication Adherence Clinical Decision Support

NCT03748420, Not applicable, Completed, HealthPartners Institute; results first posted 2024-02-26

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Medication Adherence Clinical Decision Support. Trials, record NCT03748420. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03748420

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Medication Adherence Clinical Decision Support
NCT number
NCT03748420
Status
Completed
Phases
Not applicable
Enrollment
5,421 participants, actual
Lead sponsor
HealthPartners Institute
Conditions
Hyperlipidemia, Hypertension, Diabetes, Medication Nonadherence
Interventions
Adherence Intervention
First posted
2018-11-20
Last updated
2024-02-26
Results first posted
2024-02-26
Limitations and caveats
Because this study was conducted at a single, relatively high-performing medical group, generalizability of results to other care delivery systems or patient populations is uncertain.

Source ClinicalTrials.gov

Registered outcomes6

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryBlood Pressure Medication Adherence12 months after an index visit
Number of patients who achieve a proportion of days covered (PDC) greater than or equal to 80% for at least one antihypertensive medication in each currently prescribed blood pressure medication class at 12 months following the index office visit date.
PrimaryNon-Insulin Glycemic Medication Adherence12 months after an index visit
Number of patients who achieve a proportion of days covered (PDC) greater than or equal to 80% for at least one non-insulin glycemic medication in each currently prescribed glycemic medication class at 12 months following the index office visit date.
PrimaryStatin Medication Adherence12 months after an index visitNumber of patients who achieve a proportion of days covered (PDC) greater than or equal to 80% for a statin medication if currently prescribed at 12 months following the index office visit date.
PrimaryMean Change in Systolic Blood Pressure12 months after an index visitMean change in systolic blood pressure (SBP) from index to the last SBP value within 12 months after the index visit.
PrimaryMean Change in A1c12 months after an index visitMean change in A1c (glycated hemoglobin) value from the index visit to the last lab test within 12 months after the index visit.
SecondaryClinic-based Medical Care Costs12 months after an index visitChange in annual clinic-based medical care costs, defined from the health system perspective.

Outcomes6

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYBlood Pressure Medication Adherence12 months after an index visitParticipants that were not at evidence-based goals for blood pressure (BP) and had PDC less than 80% with moderate to high confidence.ParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYNon-Insulin Glycemic Medication Adherence12 months after an index visitParticipants that were not at evidence-based goals for glucose (A1c) and had PDC less than 80% with moderate to high confidence.ParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYStatin Medication Adherence12 months after an index visitParticipants that had PDC less than 80% with moderate to high confidence.ParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYMean Change in Systolic Blood Pressure12 months after an index visitNot at evidence-based clinical goals for SBP and had proportion of days covered (PDC) greater than or equal to 80%.mm HgMEAN
PRIMARYMean Change in A1c12 months after an index visitParticipants that were not at evidence-based goals for hemoglobin A1c and had PDC less than 80% with moderate to high confidence.percentage of glycated hemoglobinMEAN
SECONDARYClinic-based Medical Care Costs12 months after an index visit
All enrolled participants that were not at evidence-based goals for blood pressure (BP) or glucose and had proportion of days covered (PDC) less than 80% with moderate to high confidence for blood pressure, glucose, or statin medications.
US dollarsMEAN

Results by group12

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Blood Pressure Medication AdherenceUsual Care396Participants
Blood Pressure Medication AdherenceAdherence Intervention470Participants
Non-Insulin Glycemic Medication AdherenceUsual Care279Participants
Non-Insulin Glycemic Medication AdherenceAdherence Intervention296Participants
Statin Medication AdherenceUsual Care529Participants
Statin Medication AdherenceAdherence Intervention586Participants
Mean Change in Systolic Blood PressureUsual Care-15.295% Confidence Interval -16.7 to -13.6mm Hg
Mean Change in Systolic Blood PressureAdherence Intervention-13.895% Confidence Interval -15.3 to -12.3mm Hg
Mean Change in A1cUsual Care-1.195% Confidence Interval -1.2 to -0.9percentage of glycated hemoglobin
Mean Change in A1cAdherence Intervention-1.295% Confidence Interval -1.4 to -1.0percentage of glycated hemoglobin

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDUsual Care2,676
Overall StudySTARTEDAdherence Intervention2,745
Overall StudyCOMPLETEDUsual Care2,421
Overall StudyCOMPLETEDAdherence Intervention2,486
Overall StudyNOT COMPLETEDUsual Care255
Overall StudyNOT COMPLETEDAdherence Intervention259

Adverse events16

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherHypoglycemiaEndocrine disordersUsual Care162,808
otherHypoglycemiaEndocrine disordersAdherence Intervention262,879
otherHypotensionVascular disordersUsual Care222,808
otherHypotensionVascular disordersAdherence Intervention162,879
otherHypokalemiaMetabolism and nutrition disordersUsual Care672,808
otherHypokalemiaMetabolism and nutrition disordersAdherence Intervention522,879
otherHyperkalemiaMetabolism and nutrition disordersUsual Care172,808
otherHyperkalemiaMetabolism and nutrition disordersAdherence Intervention122,879
otherHyponatremiaMetabolism and nutrition disordersUsual Care152,808
otherHyponatremiaMetabolism and nutrition disordersAdherence Intervention282,879

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityUsual Care242,808
Total, all-cause mortalityAdherence Intervention282,879
Total, other adverse eventsUsual Care1272,808
Total, other adverse eventsAdherence Intervention1272,879
Total, serious adverse eventsUsual Care5572,808
Total, serious adverse eventsAdherence Intervention5592,879

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
37956792DERIVEDPubMed
39786775DERIVEDPubMed

Grants1

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
R01HL136937A Team-Based and Technology Driven Adherence Intervention to Improve Chronic Disease OutcomesSPERL-HILLEN, JOANN MHEALTHPARTNERS INSTITUTENATIONAL HEART, LUNG, AND BLOOD INSTITUTE2018 to 2022

Trial comparisons5

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
Adherence Intervention vs Usual Care: Blood Pressure Medication AdherenceTrial comparisons
Adherence Intervention vs Usual Care: Non-Insulin Glycemic Medication AdherenceTrial comparisons
Adherence Intervention vs Usual Care: Statin Medication AdherenceTrial comparisons
Adherence Intervention vs Usual Care: deaths from any causeTrial comparisons
Adherence Intervention vs Usual Care: serious adverse eventsTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT03748420

GET https://conductscience.org/api/trials/v1/NCT03748420/registered